Alvotech er fjölþjóðlegt hátæknifyrirtæki í fremstu röð. Meira en 1400 starfsfólk af um 70 þjóðernum sameinast um að móta framtíðina á sviði líftæknilyfja og tryggja sjúklingum um allan heim betra aðgengi að hágæða lyfjum. Meðal starfsfólks eru margir af færustu vísindamönnum landsins.

Við leyfum fjölbreytileika, forvitni og frumkvæði starfsfólks að njóta sín. Við bjóðum aðlaðandi starfsumhverfi í stöðugri mótun og ögrandi verkefni. Alvotech tryggir að jafnrétti kynjanna til launa og frama nái til alls starfsfólks, hérlendis jafnt sem erlendis. Við viljum laða að okkur færasta fólkið á hverju sviði, án tillits til uppruna eða kyns. Með þessum hætti getum við best þjónað hagsmunum sjúklinga og samstarfsaðilum okkar. 

Vertu með okkur í að bæta lífsgæði fólks og auka aðgengi að hagkvæmum líftæknilyfjum. 


1001-5000

Meginmarkmið jafnlaunavottunar er að vinna gegn kynbundnum launamun og stuðla að jafnrétti kynjanna á vinnumarkaði.

Jafnlaunavottun

Website

Facebook

Instagram

LinkedIn

Activity

Commute

Food / meal at work

Entertainment

Work environment

Alvotech leitar a&eth; &ouml;flugum og n&aacute;kv&aelig;mum launas&eacute;rfr&aelig;&eth;ingi &iacute; t&iacute;mabundi&eth; starf til 6 m&aacute;na&eth;a me&eth; m&ouml;guleika &aacute; framlengingu.
Launateymi Alvotech annast launavinnslu fyrir um 1100 manns &aacute; &Iacute;slandi, auk umsj&oacute;nar launavinnslu &iacute; nokkrum l&ouml;ndum utan &Iacute;slands.
Starfi&eth; felur &iacute; s&eacute;r vinnslu m&aacute;na&eth;arlegra launa, ums&yacute;slu launagagna, samskipti vi&eth; starfsf&oacute;lk og stj&oacute;rnendur &aacute;samt &thorn;v&iacute; a&eth; tryggja a&eth; launavinnsla samr&aelig;mist &iacute;slenskum l&ouml;gum, kjarasamningum og skattareglum.
Vi&eth; leitum a&eth; einstaklingi me&eth; a&eth; l&aacute;gmarki 3 &aacute;ra reynslu af launavinnslu, g&oacute;&eth;a &thorn;ekkingu &aacute; &iacute;slensku launaumhverfi, skattam&aacute;lum og l&iacute;feyrism&aacute;lum. &THORN;ekking &aacute; launavinnslu &iacute; Kjarna er kostur, g&oacute;&eth; Excel-kunn&aacute;tta og h&aelig;fni til a&eth; vinna me&eth; tr&uacute;na&eth;aruppl&yacute;singar af fagmennsku eru skilyr&eth;i. Mj&ouml;g g&oacute;&eth; &iacute;slensku- og enskukunn&aacute;tta er nau&eth;synleg.
Kostur er ef ums&aelig;kjandi hefur reynslu af al&thorn;j&oacute;&eth;legri launavinnslu, umb&oacute;taverkefnum tengdum launaferlum og vinnu &iacute; hr&ouml;&eth;u og krefjandi starfsumhverfi.&nbsp;
[English]&nbsp;
Alvotech is looking for a temporary (6 months contract with the possibility of extension) Payroll Specialist. The Payroll Specialist is responsible for ensuring accurate and timely payroll processing, maintaining compliance with Icelandic labor laws, collective agreements, tax requirements, and internal policies. The role works closely with HR, Finance, managers, external payroll providers, and government authorities to deliver a high-quality payroll service to employees. Key responsibilities:
<ul>
<li>Process monthly payroll accurately and on time.</li>
<li>Review and validate payroll data, including salaries, overtime, shift premiums, bonuses, allowances, and deductions.</li>
<li>Maintain employee payroll records and ensure data accuracy within HR and payroll systems.</li>
<li>Calculate final settlements, vacation pay, and other employee payments.</li>
<li>Support payroll-related month-end and year-end activities.</li>
<li>Ensure compliance with Icelandic labor legislation, tax regulations, social security requirements, and collective bargaining agreements.</li>
<li>Maintain knowledge of relevant laws, regulations, and union requirements.</li>
<li>Prepare and submit payroll-related reports and declarations to authorities and third-party providers.</li>
<li>Support internal and external audits by providing payroll documentation and reports.</li>
<li>Respond to employee and manager inquiries regarding payroll, taxation, benefits, vacation accruals, and deductions.</li>
<li>Provide guidance and support on payroll-related matters in a professional and confidential manner.</li>
<li>Assist with onboarding and offboarding activities related to payroll administration.</li>
<li>The Payroll Specialist is responsible for ensuring accurate and timely payroll processing, maintaining compliance with Icelandic labor laws, collective agreements, tax requirements, and internal policies.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor's degree in Business Administration, Accounting, Human Resources, or a related&nbsp;field, or equivalent experience.</li>
<li>Minimum 3 years of payroll administration experience.</li>
<li>Fluent in Icelandic and English, both written and spoken.</li>
<li>Strong knowledge of Icelandic payroll practices, taxation, pension administration, and labor market requirements.</li>
<li>Experience in working with payroll and HR information systems.</li>
<li>Advanced Excel skills and experience with payroll reporting.</li>
<li>Strong attention to detail and high level of accuracy.</li>
<li>Ability to handle confidential information with discretion.</li>
<li>Experience in supporting multinational payroll operations.</li>
<li>Knowledge of collective bargaining agreements and union requirements in Iceland.</li>
<li>Experience with payroll process improvement and automation initiatives.</li>
<li>Knowledge of Kjarni payroll solutions is a strong advantage.</li>
</ul>
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>

Alvotech hf


Alvotech leitar að öflugum og nákvæmum launasérfræðingi í tímabundið starf til 6 mánaða með möguleika á framlengingu.

Launateymi Alvotech annast launavinnslu fyrir um 1100 manns á Íslandi, auk umsjónar launavinnslu í nokkrum löndum utan Íslands.

Starfið felur í sér vinnslu mánaðarlegra launa, umsýslu launagagna, samskipti við starfsfólk og stjórnendur ásamt því að tryggja að launavinnsla samræmist íslenskum lögum, kjarasamningum og skattareglum.

Við leitum að einstaklingi með að lágmarki 3 ára reynslu af launavinnslu, góða þekkingu á íslensku launaumhverfi, skattamálum og lífeyrismálum. Þekking á launavinnslu í Kjarna er kostur, góð Excel-kunnátta og hæfni til að vinna með trúnaðarupplýsingar af fagmennsku eru skilyrði. Mjög góð íslensku- og enskukunnátta er nauðsynleg.

Kostur er ef umsækjandi hefur reynslu af alþjóðlegri launavinnslu, umbótaverkefnum tengdum launaferlum og vinnu í hröðu og krefjandi starfsumhverfi.


[English]


Alvotech is looking for a temporary (6 months contract with the possibility of extension) Payroll Specialist. The Payroll Specialist is responsible for ensuring accurate and timely payroll processing, maintaining compliance with Icelandic labor laws, collective agreements, tax requirements, and internal policies. The role works closely with HR, Finance, managers, external payroll providers, and government authorities to deliver a high-quality payroll service to employees.

Key responsibilities:


 - Process monthly payroll accurately and on time.

 - Review and validate payroll data, including salaries, overtime, shift premiums, bonuses, allowances, and deductions.

 - Maintain employee payroll records and ensure data accuracy within HR and payroll systems.

 - Calculate final settlements, vacation pay, and other employee payments.

 - Support payroll-related month-end and year-end activities.

 - Ensure compliance with Icelandic labor legislation, tax regulations, social security requirements, and collective bargaining agreements.

 - Maintain knowledge of relevant laws, regulations, and union requirements.

 - Prepare and submit payroll-related reports and declarations to authorities and third-party providers.

 - Support internal and external audits by providing payroll documentation and reports.

 - Respond to employee and manager inquiries regarding payroll, taxation, benefits, vacation accruals, and deductions.

 - Provide guidance and support on payroll-related matters in a professional and confidential manner.

 - Assist with onboarding and offboarding activities related to payroll administration.

 - The Payroll Specialist is responsible for ensuring accurate and timely payroll processing, maintaining compliance with Icelandic labor laws, collective agreements, tax requirements, and internal policies.


Qualifications:


 - Bachelor's degree in Business Administration, Accounting, Human Resources, or a related
field, or equivalent experience.

 - Minimum 3 years of payroll administration experience.

 - Fluent in Icelandic and English, both written and spoken.

 - Strong knowledge of Icelandic payroll practices, taxation, pension administration, and labor market requirements.

 - Experience in working with payroll and HR information systems.

 - Advanced Excel skills and experience with payroll reporting.

 - Strong attention to detail and high level of accuracy.

 - Ability to handle confidential information with discretion.

 - Experience in supporting multinational payroll operations.

 - Knowledge of collective bargaining agreements and union requirements in Iceland.

 - Experience with payroll process improvement and automation initiatives.

 - Knowledge of Kjarni payroll solutions is a strong advantage.


What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


Active

Payroll Specialist

Vi&eth; leitum a&eth; &aacute;hugas&ouml;mum einstaklingi til a&eth; ganga til li&eth;s vi&eth; Visual Inspection teymi&eth; okkar &iacute; framlei&eth;slunni. Starfi&eth; felst &iacute; sj&oacute;nr&aelig;nni g&aelig;&eth;asko&eth;un &aacute; fullb&uacute;nu l&iacute;ft&aelig;knilyfi &iacute; reglubundnu umhverfi. Um er a&eth; r&aelig;&eth;a vaktavinnu. &AElig;skilegt er a&eth; ums&aelig;kjandi s&eacute; n&aacute;kv&aelig;mur og me&eth; gott auga fyrir sm&aacute;atri&eth;um. 
[English] 
We are seeking a Technologist to join our Visual Inspection team, responsible for performing visual inspection of pharmaceutical products in a controlled, non-classified (CNC) environment. This is a shift‑based position, requiring flexibility and availability for assigned shifts. The ideal candidate shows strong attention to detail, patience, and strict adherence to procedures, including cGMP and EHS requirements. 
Key Responsibilities
<ul>
<li>
Perform visual inspection of final pharmaceutical products in&nbsp;controlled/non-classified&nbsp;areas (CNC) in accordance with approved procedures
</li>
<li>
Package final products post-inspection in compliance with established procedures
</li>
<li>
Role may require lifting and handling heavy boxes
</li>
<li>
Use computer systems and software to document inspection activities accurately and in compliance with cGMP and data integrity requirements.
</li>
<li>
Support in GMP production activities, including technical and validation support when required
</li>
<li>
Conduct all activities in full compliance with cGMP, EHS, and company quality systems
</li>
<li>
Adhere strictly to SOPs, work instructions, and job-specific procedures
</li>
<li>
Support and contribute, as required, to audits, inspections, and regulatory interactions, including Pre-Approval Inspections (PAIs)
</li>
<li>
Work performed in a dark room designed for visual inspection 
</li>
</ul>
Qualifications
<ul>
<li>
Strong attention to detail, high concentration, and the ability to perform repetitive tasks accurately.
</li>
<li>
Solid understanding of written procedures and commitment to following cGMP, EHS, SOPs, and quality standards.
</li>
<li>
Proficiency in using computers and standard software tools for documentation and daily operations.
</li>
<li>
Team-oriented mindset with the ability to follow guidance and work collaboratively.
</li>
<li>
Basic technical or administrative knowledge relevant to manufacturing environments.
</li>
<li>
Basic knowledge of GMP manufacturing operations; 1&ndash;2 years of experience in technical or production roles is an advantage.
</li>
<li>
Passing a vision test with good eyesight (with or without corrective lenses) is a mandatory&nbsp;for this position.
</li>
</ul>
Successful candidates must demonstrate visual capability suitable for manual visual inspection. This position is critical to product quality and patient safety and requires consistent performance and procedural discipline. What we offer:
<ul>
<li>
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
</li>
<li>
The chance to be a part of a global and fast-growing company.
</li>
<li>
An international work culture that encourages diversity, collaboration and inclusion.
</li>
<li>
Positive, flexible, and innovative work environment.
</li>
<li>
Support for personal growth and internal career development.
</li>
<li>
Company social events and milestone celebrations.
</li>
<li>
Excellent in-house canteen and coffee house.
</li>
<li>
Exercise and wellbeing support for full-time employees.
</li>
<li>
On-site shower facility.
</li>
<li>
Transportation grant towards eco-friendly modes of travel for full-time employees.
</li>
<li>
Internet at home for full-time employees. At Alvotech, we're committed to fostering a diverse and inclusive workplace where everyone feels valued, respected, and empowered to succeed. We encourage applications from all qualified candidates. However, relocation assistance /Work sponsorship is not available for this role
</li>
</ul>
Why Alvotech
At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We&rsquo;re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.
True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let&rsquo;s create a healthier world together, through affordable biologic medicines.


Við leitum að áhugasömum einstaklingi til að ganga til liðs við Visual Inspection teymið okkar í framleiðslunni. Starfið felst í sjónrænni gæðaskoðun á fullbúnu líftæknilyfi í reglubundnu umhverfi. Um er að ræða vaktavinnu. Æskilegt er að umsækjandi sé nákvæmur og með gott auga fyrir smáatriðum.



[English]



We are seeking a Technologist to join our Visual Inspection team, responsible for performing visual inspection of pharmaceutical products in a controlled, non-classified (CNC) environment. This is a shift‑based position, requiring flexibility and availability for assigned shifts. The ideal candidate shows strong attention to detail, patience, and strict adherence to procedures, including cGMP and EHS requirements.



Key Responsibilities


 - 

Perform visual inspection of final pharmaceutical products in
controlled/non-classified
areas (CNC) in accordance with approved procedures


 - 

Package final products post-inspection in compliance with established procedures


 - 

Role may require lifting and handling heavy boxes


 - 

Use computer systems and software to document inspection activities accurately and in compliance with cGMP and data integrity requirements.


 - 

Support in GMP production activities, including technical and validation support when required


 - 

Conduct all activities in full compliance with cGMP, EHS, and company quality systems


 - 

Adhere strictly to SOPs, work instructions, and job-specific procedures


 - 

Support and contribute, as required, to audits, inspections, and regulatory interactions, including Pre-Approval Inspections (PAIs)


 - 

Work performed in a dark room designed for visual inspection





Qualifications


 - 

Strong attention to detail, high concentration, and the ability to perform repetitive tasks accurately.


 - 

Solid understanding of written procedures and commitment to following cGMP, EHS, SOPs, and quality standards.


 - 

Proficiency in using computers and standard software tools for documentation and daily operations.


 - 

Team-oriented mindset with the ability to follow guidance and work collaboratively.


 - 

Basic technical or administrative knowledge relevant to manufacturing environments.


 - 

Basic knowledge of GMP manufacturing operations; 1–2 years of experience in technical or production roles is an advantage.


 - 

Passing a vision test with good eyesight (with or without corrective lenses) is a mandatory
for this position.



Successful candidates must demonstrate visual capability suitable for manual visual inspection. This position is critical to product quality and patient safety and requires consistent performance and procedural discipline.

What we offer:


 - 

An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.


 - 

The chance to be a part of a global and fast-growing company.


 - 

An international work culture that encourages diversity, collaboration and inclusion.


 - 

Positive, flexible, and innovative work environment.


 - 

Support for personal growth and internal career development.


 - 

Company social events and milestone celebrations.


 - 

Excellent in-house canteen and coffee house.


 - 

Exercise and wellbeing support for full-time employees.


 - 

On-site shower facility.


 - 

Transportation grant towards eco-friendly modes of travel for full-time employees.


 - 

Internet at home for full-time employees.

At Alvotech, we're committed to fostering a diverse and inclusive workplace where everyone feels valued, respected, and empowered to succeed. We encourage applications from all qualified candidates. However, relocation assistance /Work sponsorship is not available for this role



Why Alvotech

At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.

True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together, through affordable biologic medicines.



Sérfræðingur í sjónrænni gæðaskoðun / Visual Inspection Technologist

An Associate scientist in the Quality Control Product testing team plays a vital part at Alvotech by participating in the quality control and release of products manufactured at Alvotech. We are looking for an individual who has a positive attitude, embraces challenges, is flexible and adaptive, and shares our values of team spirit and team efforts.

Scope and responsibility:
<ul>
<li>Performs routine analytical testing with analytical techniques such as Liquid Chromatography (SEC, APAC, CEX, etc.), Capillary electrophoresis (iCIEF, CE-SDS), compendial methods (colour, clarity, subvisible particles, TOC, etc.) and reviews analytical test records to support manufacturing process with limited supervision.</li>
</ul>
<ul>
<li>Execute routine laboratory activities, including equipment cleaning, verification, stock management, and general laboratory maintenance to ensure operational readiness and compliance.</li>
<li>Performing activities required to support testing, e.g., buffer preparation</li>
</ul>
<ul>
<li>Participate in the creation and maintenance of quality documents within Alvotech.</li>
<li>Contributes to other documentation reviews and/or updates within the Quality management system.</li>
</ul>
Job requirements:
<ul>
<li>Bachelor&rsquo;s degree or master&rsquo;s degree in a relevant scientific discipline and at least 0-1 years of relevant experience in the pharmaceutical or biopharmaceutical sector.</li>
<li>Proficient in using a PC and common Microsoft packages such as Word and Excel.</li>
<li>Basic Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset.</li>
</ul>
&nbsp;
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration, and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and well-being support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
&nbsp;
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


An Associate scientist in the Quality Control Product testing team plays a vital part at Alvotech by participating in the quality control and release of products manufactured at Alvotech. We are looking for an individual who has a positive attitude, embraces challenges, is flexible and adaptive, and shares our values of team spirit and team efforts.



Scope and responsibility:


 - Performs routine analytical testing with analytical techniques such as Liquid Chromatography (SEC, APAC, CEX, etc.), Capillary electrophoresis (iCIEF, CE-SDS), compendial methods (colour, clarity, subvisible particles, TOC, etc.) and reviews analytical test records to support manufacturing process with limited supervision.



 - Execute routine laboratory activities, including equipment cleaning, verification, stock management, and general laboratory maintenance to ensure operational readiness and compliance.

 - Performing activities required to support testing, e.g., buffer preparation



 - Participate in the creation and maintenance of quality documents within Alvotech.

 - Contributes to other documentation reviews and/or updates within the Quality management system.


Job requirements:


 - Bachelor’s degree or master’s degree in a relevant scientific discipline and at least 0-1 years of relevant experience in the pharmaceutical or biopharmaceutical sector.

 - Proficient in using a PC and common Microsoft packages such as Word and Excel.

 - Basic Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset.





What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration, and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and well-being support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.





About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

Associate Scientist - QC Product testing

Key responsibilities and minimum requirements according to the role:
&bull; Provide QA oversight and collaborate with cross-functional teams in planning maintenance, qualification, and validation activities for facilities, utilities, equipment, and computer systems (CSV).
&bull; Serve as a Quality representative and a subject matter expert (SME) in selection, design and build of new technologies and new facilities within Alvotech.
&bull; Support and provide QA oversight with review and approval of qualification documents for facility, utility, equipment and computerized systems as applicable.
&bull; Contribute to investigations into discrepancies arising during qualification / validation activities and subsequent approval of appropriate corrective actions.
&bull; Review of planned and unplanned work orders for maintenance, preventive maintenance, calibrations and other Engineering related activities.
&bull; Reviews and approve change controls, deviations , CAPAs , effectiveness checks for facilities, utilities, and equipment, computer systems.
&bull; Stay current on applicable external requirements and industry standards and drive continuous
improvement on Engineering and CSV processes and tools.
&bull; Advice on quality matters, and assistance for closing compliance gaps found in audits and
inspections.
&bull; Escalation of any data integrity or critical quality issues to the supervisor and Quality Management of Alvotech
&bull; Responsible for ensuring all facilities, utilities, equipment , computer systems are appropriately validated and qualification in line with current EU and US legislation for parenteral/biologics.
Minimum education and experience required for the role:
&bull; A bachelor&rsquo;s degree within relevant area, or other relevant business experience
&bull; Minimum 5 years of experience within the Pharmaceutical or Medical Device Industry (preferably in parenteral/biologics formulations).
&bull; Experience working with regulatory requirements in GxP required (Preferably FDA and EU regulations).
&bull; Good understanding of GAMP 5 guide required.
&bull; Knowledge of and experience with validation and qualification specifically within facility, utility, and equipment/computer systems.
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


Key responsibilities and minimum requirements according to the role:

• Provide QA oversight and collaborate with cross-functional teams in planning maintenance, qualification, and validation activities for facilities, utilities, equipment, and computer systems (CSV).

• Serve as a Quality representative and a subject matter expert (SME) in selection, design and build of new technologies and new facilities within Alvotech.

• Support and provide QA oversight with review and approval of qualification documents for facility, utility, equipment and computerized systems as applicable.

• Contribute to investigations into discrepancies arising during qualification / validation activities and subsequent approval of appropriate corrective actions.

• Review of planned and unplanned work orders for maintenance, preventive maintenance, calibrations and other Engineering related activities.

• Reviews and approve change controls, deviations , CAPAs , effectiveness checks for facilities, utilities, and equipment, computer systems.

• Stay current on applicable external requirements and industry standards and drive continuous

improvement on Engineering and CSV processes and tools.

• Advice on quality matters, and assistance for closing compliance gaps found in audits and

inspections.

• Escalation of any data integrity or critical quality issues to the supervisor and Quality Management of Alvotech

• Responsible for ensuring all facilities, utilities, equipment , computer systems are appropriately validated and qualification in line with current EU and US legislation for parenteral/biologics.

Minimum education and experience required for the role:

• A bachelor’s degree within relevant area, or other relevant business experience

• Minimum 5 years of experience within the Pharmaceutical or Medical Device Industry (preferably in parenteral/biologics formulations).

• Experience working with regulatory requirements in GxP required (Preferably FDA and EU regulations).

• Good understanding of GAMP 5 guide required.

• Knowledge of and experience with validation and qualification specifically within facility, utility, and equipment/computer systems.

What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

Principal Specialist - QA Engineering

Latest jobs

Visual Inspection Technologist

Alvotech is looking for a Power Platform &amp; AI Developer
 What you will do
<ul>
<li>Power Apps: build canvas and model-driven apps with clean UX, delegation-aware formulas, reusable components and role-based security.</li>
<li>Power Automate: design cloud flows for approvals, notifications, data sync and system integrations, with proper error handling, retries and logging.</li>
<li>SQL databases: design schemas, write views, stored procedures and queries in SQL Server / Azure SQL; tune performance and maintain data quality.</li>
<li>Dataverse: model tables, relationships and business rules; manage solutions and environment security.</li>
<li>AI agents: build and deploy agents and copilots in Copilot Studio, including grounding on company data, prompt design, tool/connector actions and guardrails.</li>
<li>Integrations: connect apps and flows to enterprise systems and data sources using OData, REST APIs and custom connectors.</li>
<li>Secure development: apply secure coding practices, including least-privilege access, safe handling of secrets and credentials, input validation and protection of sensitive data.</li>
<li>ALM and DevOps: use Azure DevOps for source control, work items and CI/CD pipelines; use solutions, environment variables and connection references to move work from dev to test to production; follow DLP and security policies.</li>
<li>Documentation and support: write technical docs and user guides, train users, and troubleshoot production issues.</li>
</ul>

Required qualifications
<ul>
<li>3+ years building production solutions on Microsoft Power Platform (Power Apps and Power Automate).</li>
<li>Strong SQL: schema design, joins, views, stored procedures, indexing and query tuning.</li>
<li>Solid Power Fx and working knowledge of Dataverse.</li>
<li>Experience integrating with REST APIs, OData services and custom connectors; comfortable with JSON.</li>
<li>Hands-on experience building at least one AI agent or LLM-powered solution (Copilot Studio, Azure OpenAI or similar).</li>
<li>Understanding of Power Platform ALM: solutions, environments, managed vs unmanaged deployment.</li>
<li>Working experience with Azure DevOps (Repos, Boards, Pipelines) or a similar DevOps toolset.</li>
<li>Awareness of secure coding principles and common security risks in apps, APIs and integrations.</li>
<li>Able to gather requirements from non-technical users and turn them into clear designs.</li>
<li>Clear written and spoken English; works independently and manages own priorities.</li>
</ul>

Nice to have
<ul>
<li>SAP S/4HANA integration experience (OData, CDS views, BAPIs).</li>
<li>Azure services: Functions, Logic Apps, Azure SQL, AI Search, Key Vault.</li>
<li>Power BI and DAX; data migration or ETL experience.</li>
<li>Agent frameworks and patterns: RAG, MCP, Semantic Kernel or similar; n8n.</li>
<li>Power Pages or external-facing portals.</li>
<li>Experience in a regulated industry (pharma / life sciences, GxP, validated systems).</li>
<li>Microsoft certifications such as PL-400, PL-600 or AI-102.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.


Alvotech is looking for a Power Platform &amp; AI Developer


What you will do


 - Power Apps: build canvas and model-driven apps with clean UX, delegation-aware formulas, reusable components and role-based security.

 - Power Automate: design cloud flows for approvals, notifications, data sync and system integrations, with proper error handling, retries and logging.

 - SQL databases: design schemas, write views, stored procedures and queries in SQL Server / Azure SQL; tune performance and maintain data quality.

 - Dataverse: model tables, relationships and business rules; manage solutions and environment security.

 - AI agents: build and deploy agents and copilots in Copilot Studio, including grounding on company data, prompt design, tool/connector actions and guardrails.

 - Integrations: connect apps and flows to enterprise systems and data sources using OData, REST APIs and custom connectors.

 - Secure development: apply secure coding practices, including least-privilege access, safe handling of secrets and credentials, input validation and protection of sensitive data.

 - ALM and DevOps: use Azure DevOps for source control, work items and CI/CD pipelines; use solutions, environment variables and connection references to move work from dev to test to production; follow DLP and security policies.

 - Documentation and support: write technical docs and user guides, train users, and troubleshoot production issues.




Required qualifications


 - 3+ years building production solutions on Microsoft Power Platform (Power Apps and Power Automate).

 - Strong SQL: schema design, joins, views, stored procedures, indexing and query tuning.

 - Solid Power Fx and working knowledge of Dataverse.

 - Experience integrating with REST APIs, OData services and custom connectors; comfortable with JSON.

 - Hands-on experience building at least one AI agent or LLM-powered solution (Copilot Studio, Azure OpenAI or similar).

 - Understanding of Power Platform ALM: solutions, environments, managed vs unmanaged deployment.

 - Working experience with Azure DevOps (Repos, Boards, Pipelines) or a similar DevOps toolset.

 - Awareness of secure coding principles and common security risks in apps, APIs and integrations.

 - Able to gather requirements from non-technical users and turn them into clear designs.

 - Clear written and spoken English; works independently and manages own priorities.




Nice to have


 - SAP S/4HANA integration experience (OData, CDS views, BAPIs).

 - Azure services: Functions, Logic Apps, Azure SQL, AI Search, Key Vault.

 - Power BI and DAX; data migration or ETL experience.

 - Agent frameworks and patterns: RAG, MCP, Semantic Kernel or similar; n8n.

 - Power Pages or external-facing portals.

 - Experience in a regulated industry (pharma / life sciences, GxP, validated systems).

 - Microsoft certifications such as PL-400, PL-600 or AI-102.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.

Power Platform & AI Developer

Alvotech is looking for a SAP Functional Analyst &ndash; Manufacturing, Quality &amp; PP/DS This position sits in the IT department as part of the SAP team. The SAP Functional Analyst is the IT owner of the SAP S/4HANA processes that run manufacturing and quality: Production Planning (PP), Quality Management (QM) and Production Planning &amp; Detailed Scheduling (PP/DS).

The role is the link between the business and the system. You will work closely with Manufacturing, Quality and Supply Chain key users to understand how they work, keep the SAP solution stable and compliant, and improve it over time. That means resolving incidents, analyzing and designing changes, configuring the system, and making sure every change is properly tested, documented and validated before it reaches production.

This is a hands-on functional role in a regulated (GMP) manufacturing environment. You will not run the shop floor or the quality function yourself, but you need to understand them well enough to translate their needs into a reliable SAP solution and to challenge requirements where a better system approach exists.

Key responsibilities
Application support and operations
&bull; Provide functional support for SAP S/4HANA, with primary focus on QM, PP and PP/DS.
&bull; Support manufacturing and quality processes including production/process orders, master recipes, BOMs, work centers/resources, inspection lots, results recording, usage decisions and batch management.
&bull; Analyze incidents, perform root-cause analysis and resolve issues within agreed service levels, escalating to SAP technical resources or external partners where needed.
&bull; Provide day-to-day support and guidance to Manufacturing, Supply Chain and Quality key users.

Planning and scheduling (PP/DS)
&bull; Support and optimize PP/DS planning and scheduling, including heuristics, planning runs, alerts and planning issues.
&bull; Manage master-data dependencies and the integration between PP/DS and core S/4HANA (orders, resources, recipes, stock and demand).

Change and continuous improvement
&bull; Gather and analyze business requirements and define the appropriate SAP configuration or functional enhancement.
&bull; Translate requirements into functional specifications and coordinate development with SAP technical resources and external consultants.
&bull; Own SAP change requests end to end: impact assessment, configuration, functional and regression testing, UAT coordination and deployment to production.
&bull; Lead smaller SAP enhancements and improvement initiatives within the QM / PP / PP-DS area, and contribute to larger projects and rollouts.

Compliance, documentation and training
&bull; Follow GMP and computerized-system validation (CSV) requirements, including change control, test evidence and deviation handling for SAP changes.
&bull; Maintain functional documentation, SOP-related system documentation and end-user training material.
&bull; Train key users and end users on new and changed functionality.

Minimum requirements
&bull; BS/BA degree in Information Systems, Engineering, Supply Chain, Life Sciences or equivalent relevant education.
&bull; Minimum 5 years of SAP functional experience, preferably within SAP PP, QM and/or PP/DS.
&bull; Experience supporting SAP S/4HANA in a productive manufacturing environment.
&bull; Hands-on configuration experience in at least one of PP, QM or PP/DS.
&bull; Good understanding of manufacturing, quality and production-planning processes.
&bull; Strong analytical, problem-solving and stakeholder-management skills.
&bull; Fluent written and spoken English.

Preferred qualifications
&bull; Experience in a GMP-regulated industry (pharmaceutical, biotech or medical devices) and with computer-system validation.
&bull; Experience with process manufacturing (process orders, master recipes, batch management).
&bull; Knowledge of related modules and integrations, e.g. MM, WM/EWM, PM and MES or LIMS interfaces.
&bull; Experience working with external SAP partners and an ITIL-based support model.
&bull; SAP certification in PP, QM or PP/DS.

Personal attributes
&bull; Takes ownership of issues and follows them through to resolution.
&bull; Communicates clearly with both business users and technical teams.
&bull; Structured and detail-oriented, with a strong sense for quality and compliance.
&bull; Comfortable balancing day-to-day support with improvement work.


Alvotech is looking for a SAP Functional Analyst – Manufacturing, Quality &amp; PP/DS
This position sits in the IT department as part of the SAP team. The SAP Functional Analyst is the IT owner of the SAP S/4HANA processes that run manufacturing and quality: Production Planning (PP), Quality Management (QM) and Production Planning &amp; Detailed Scheduling (PP/DS).



The role is the link between the business and the system. You will work closely with Manufacturing, Quality and Supply Chain key users to understand how they work, keep the SAP solution stable and compliant, and improve it over time. That means resolving incidents, analyzing and designing changes, configuring the system, and making sure every change is properly tested, documented and validated before it reaches production.



This is a hands-on functional role in a regulated (GMP) manufacturing environment. You will not run the shop floor or the quality function yourself, but you need to understand them well enough to translate their needs into a reliable SAP solution and to challenge requirements where a better system approach exists.



Key responsibilities

Application support and operations

• Provide functional support for SAP S/4HANA, with primary focus on QM, PP and PP/DS.

• Support manufacturing and quality processes including production/process orders, master recipes, BOMs, work centers/resources, inspection lots, results recording, usage decisions and batch management.

• Analyze incidents, perform root-cause analysis and resolve issues within agreed service levels, escalating to SAP technical resources or external partners where needed.

• Provide day-to-day support and guidance to Manufacturing, Supply Chain and Quality key users.



Planning and scheduling (PP/DS)

• Support and optimize PP/DS planning and scheduling, including heuristics, planning runs, alerts and planning issues.

• Manage master-data dependencies and the integration between PP/DS and core S/4HANA (orders, resources, recipes, stock and demand).



Change and continuous improvement

• Gather and analyze business requirements and define the appropriate SAP configuration or functional enhancement.

• Translate requirements into functional specifications and coordinate development with SAP technical resources and external consultants.

• Own SAP change requests end to end: impact assessment, configuration, functional and regression testing, UAT coordination and deployment to production.

• Lead smaller SAP enhancements and improvement initiatives within the QM / PP / PP-DS area, and contribute to larger projects and rollouts.



Compliance, documentation and training

• Follow GMP and computerized-system validation (CSV) requirements, including change control, test evidence and deviation handling for SAP changes.

• Maintain functional documentation, SOP-related system documentation and end-user training material.

• Train key users and end users on new and changed functionality.



Minimum requirements

• BS/BA degree in Information Systems, Engineering, Supply Chain, Life Sciences or equivalent relevant education.

• Minimum 5 years of SAP functional experience, preferably within SAP PP, QM and/or PP/DS.

• Experience supporting SAP S/4HANA in a productive manufacturing environment.

• Hands-on configuration experience in at least one of PP, QM or PP/DS.

• Good understanding of manufacturing, quality and production-planning processes.

• Strong analytical, problem-solving and stakeholder-management skills.

• Fluent written and spoken English.



Preferred qualifications

• Experience in a GMP-regulated industry (pharmaceutical, biotech or medical devices) and with computer-system validation.

• Experience with process manufacturing (process orders, master recipes, batch management).

• Knowledge of related modules and integrations, e.g. MM, WM/EWM, PM and MES or LIMS interfaces.

• Experience working with external SAP partners and an ITIL-based support model.

• SAP certification in PP, QM or PP/DS.



Personal attributes

• Takes ownership of issues and follows them through to resolution.

• Communicates clearly with both business users and technical teams.

• Structured and detail-oriented, with a strong sense for quality and compliance.

• Comfortable balancing day-to-day support with improvement work.

SAP Functional Analyst – Manufacturing, Quality & PP/DS

Alvotech is looking for a QA professional supporting combination product and devices R&amp;D and Design Control activities, responsible for the review and approval of quality documentation throughout the product development lifecycle, ensuring compliance with 21 CFR Part 820 and ISO 13485 requirements. Partners closely with R&amp;D teams to provide quality guidance, promote compliance, and support the effective execution of quality procedures. Contributes to the development and continuous improvement of the Quality Management System, authors and reviews quality procedures, leads cross-functional quality initiatives, supports regulatory inspections and health authority interactions, and independently manages quality improvement projects.
Specifics of the role:
<ul>
<li>Execute QA review and approval of various quality related documents generated by CPD R&amp;D during all stages of device design control (DHF, risk management files, and other associated documentation) in a 21 CFR Part 820/ISO 13485 compliant QMS.</li>
<li>Collaborate with R&amp;D partners in daily compliance activities and coach in executing quality related procedures.</li>
<li>Contribute to, author, review and approve procedures, and other supporting documents related to CPD processes.</li>
<li>Contribute as required in design, deployment, and improvements of the phase appropriate Quality Management System (QMS).</li>
<li>Routinely leads cross functional projects and performs variety of tasks of variable complexity.</li>
<li>Contribute as required in internal and health authority inspections and any other interactions with regulatory agencies.</li>
<li>Execute Quality projects independently as assigned.</li>
<li>Subject matter expert within field (device design control).</li>
<li>Main scope is internal CPD projects requiring expert QA support</li>
<li>Quality oversight and support of design control development and validation activities across the entire combination product development lifecycle.</li>
<li>R&amp;D Quality compliance SME responsible in all phases of the device design control process from concept/feasibility/planning through commercial product lifecycle management</li>
<li>Application of phase appropriate cGMP design control across the product development lifecycle within the R&amp;D, Quality Management System (QMS), with a specific focus on injectable biosimilar Combination Products and Devices.</li>
<li>High level of independence and accountability for QA project support according to CPD timelines.</li>
<li>Performs variety of tasks of variable complexity.</li>
<li>Participates in large strategic or developmental projects.</li>
<li>Challenges and decisions faced in the role are often non-precedent.</li>
<li>Can have impact on large, important projects.</li>
</ul>
Education and Experience:&nbsp;
<ul>
<li>Bachelor&lsquo;s/Master&lsquo;s degree in chemistry, biochemistry, biotechnology or equivalent.&nbsp;</li>
<li>Minimum 5 -10 years' experience in a quality assurance function supporting devices and /or&nbsp; combination products&nbsp;</li>
<li>Strong working knowledge of ISO 13485/FDA 21 CFR Part 4 and Part 820.&nbsp;</li>
<li>Proficient in Quality system processes such as CAPA, Change controls, Investigations, and&nbsp; document management, etc.&nbsp;</li>
<li>Knowledge of physical device testing and characterization methods.&nbsp;</li>
<li>Knowledge of physiochemical/bioanalytical methods is a strong plus&nbsp;</li>
<li>Thorough understanding of regulatory GxP requirements and risk management principles&nbsp;</li>
<li>Experience in supporting regulatory audits including FDA and EMA is highly desirable.</li>
<li>Prior experience of using Veeva Quality system is a strong plus.</li>
</ul>
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>


Alvotech is looking for a QA professional supporting combination product and devices R&amp;D and Design Control activities, responsible for the review and approval of quality documentation throughout the product development lifecycle, ensuring compliance with 21 CFR Part 820 and ISO 13485 requirements. Partners closely with R&amp;D teams to provide quality guidance, promote compliance, and support the effective execution of quality procedures. Contributes to the development and continuous improvement of the Quality Management System, authors and reviews quality procedures, leads cross-functional quality initiatives, supports regulatory inspections and health authority interactions, and independently manages quality improvement projects.

Specifics of the role:


 - Execute QA review and approval of various quality related documents generated by CPD R&amp;D during all stages of device design control (DHF, risk management files, and other associated documentation) in a 21 CFR Part 820/ISO 13485 compliant QMS.

 - Collaborate with R&amp;D partners in daily compliance activities and coach in executing quality related procedures.

 - Contribute to, author, review and approve procedures, and other supporting documents related to CPD processes.

 - Contribute as required in design, deployment, and improvements of the phase appropriate Quality Management System (QMS).

 - Routinely leads cross functional projects and performs variety of tasks of variable complexity.

 - Contribute as required in internal and health authority inspections and any other interactions with regulatory agencies.

 - Execute Quality projects independently as assigned.

 - Subject matter expert within field (device design control).

 - Main scope is internal CPD projects requiring expert QA support

 - Quality oversight and support of design control development and validation activities across the entire combination product development lifecycle.

 - R&amp;D Quality compliance SME responsible in all phases of the device design control process from concept/feasibility/planning through commercial product lifecycle management

 - Application of phase appropriate cGMP design control across the product development lifecycle within the R&amp;D, Quality Management System (QMS), with a specific focus on injectable biosimilar Combination Products and Devices.

 - High level of independence and accountability for QA project support according to CPD timelines.

 - Performs variety of tasks of variable complexity.

 - Participates in large strategic or developmental projects.

 - Challenges and decisions faced in the role are often non-precedent.

 - Can have impact on large, important projects.


Education and Experience:



 - Bachelor‘s/Master‘s degree in chemistry, biochemistry, biotechnology or equivalent.


 - Minimum 5 -10 years' experience in a quality assurance function supporting devices and /or

combination products


 - Strong working knowledge of ISO 13485/FDA 21 CFR Part 4 and Part 820.


 - Proficient in Quality system processes such as CAPA, Change controls, Investigations, and

document management, etc.


 - Knowledge of physical device testing and characterization methods.


 - Knowledge of physiochemical/bioanalytical methods is a strong plus


 - Thorough understanding of regulatory GxP requirements and risk management principles


 - Experience in supporting regulatory audits including FDA and EMA is highly desirable.

 - Prior experience of using Veeva Quality system is a strong plus.


What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.






QCPD Specialist

Manufacturing eSystems Specialist
&nbsp;
Scope and Responsibilities:
<ul>
<li>Manufacturing Administration: Manage electronic execution systems, including but not limited to:
<ul>
<li>Master Control Electronic Batch Records for (DS): USP, DSP, and Dispensing</li>
<li>SAP for manufacturing</li>
<li>eLogbooks in manufacturing.</li>
</ul>
</li>
<li>Oversight Duties : Oversee the creation, upkeep, and review of:
<ul>
<li>Electronic Batch Records for USP, DSP, and Dispensing</li>
<li>If required, SAP Master Recipes, Process orders, Reservations and Consumption process &minus; Electronic Logbooks for USP, DSP, and Dispensing</li>
<li>Veeva documentation required for eBR and eSystems (CC, CAPA, DEV)</li>
</ul>
</li>
</ul>
Oversight duties are being performed in collaboration with Subject Matter Expert from each manufacturing function and with collaboration with Quality Assurance.
<ul>
<li>Training: Provide training to company employees in the use of eSystems where required and relevant to eSystems requirements.</li>
<li>Scalability: Adapt to the administration of new eSystems as they are introduced into manufacturing.</li>
<li>Innovative Improvements:
<ul>
<li>Initiate and implement innovative improvements for the systems in use.</li>
<li>Act as a Subject Matter Expert (SME) for validation and qualification documentation, and collaborate cross-functionally with IT to test and implement innovative solutions, enhance operational efficiency, and ensure compliance with applicable quality standards.</li>
</ul>
</li>
<li>Independently implement and deliver assigned projects, ensuring timely completion and compliance with quality standards.</li>
<li>Contribute to team objectives through effective collaboration, knowledge sharing, and teamwork.</li>
</ul>

Job requirements:
<ul>
<li>BSc or Diploma in a Technical Discipline (e.g., pharmacy, biotechnology, biochemistry, engineering, or a related field).</li>
<li>Preferably 3-5 years of experience in pharmaceutical industry or other related &nbsp;industries.</li>
<li>Team player with strong organizational skills.</li>
<li>Excellent written and verbal communication skills.</li>
<li>Proficient in use of a PC and common Microsoft packages such as Word, Visio, Excel.</li>
<li>Excellent command of English language, both written and verbal.&nbsp;</li>
</ul>

What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.&nbsp;&nbsp;</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


Manufacturing eSystems Specialist




Scope and Responsibilities:


 - Manufacturing Administration: Manage electronic execution systems, including but not limited to:


 - Master Control Electronic Batch Records for (DS): USP, DSP, and Dispensing

 - SAP for manufacturing

 - eLogbooks in manufacturing.



 - Oversight Duties : Oversee the creation, upkeep, and review of:


 - Electronic Batch Records for USP, DSP, and Dispensing

 - If required, SAP Master Recipes, Process orders, Reservations and Consumption process − Electronic Logbooks for USP, DSP, and Dispensing

 - Veeva documentation required for eBR and eSystems (CC, CAPA, DEV)




Oversight duties are being performed in collaboration with Subject Matter Expert from each manufacturing function and with collaboration with Quality Assurance.


 - Training: Provide training to company employees in the use of eSystems where required and relevant to eSystems requirements.

 - Scalability: Adapt to the administration of new eSystems as they are introduced into manufacturing.

 - Innovative Improvements:


 - Initiate and implement innovative improvements for the systems in use.

 - Act as a Subject Matter Expert (SME) for validation and qualification documentation, and collaborate cross-functionally with IT to test and implement innovative solutions, enhance operational efficiency, and ensure compliance with applicable quality standards.



 - Independently implement and deliver assigned projects, ensuring timely completion and compliance with quality standards.

 - Contribute to team objectives through effective collaboration, knowledge sharing, and teamwork.




Job requirements:


 - BSc or Diploma in a Technical Discipline (e.g., pharmacy, biotechnology, biochemistry, engineering, or a related field).

 - Preferably 3-5 years of experience in pharmaceutical industry or other related 
industries.

 - Team player with strong organizational skills.

 - Excellent written and verbal communication skills.

 - Proficient in use of a PC and common Microsoft packages such as Word, Visio, Excel.

 - Excellent command of English language, both written and verbal.





What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.




About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

Manufacturing eSystems Specialist

Gakktu til li&eth;s vi&eth; framlei&eth;sluteymi hj&aacute; Alvotech &iacute; Reykjav&iacute;k!&nbsp;Alvotech starfar &iacute; reglubundnu umhverfi &thorn;ar sem n&aacute;kv&aelig;mni og samviskusemi skipta sk&ouml;pum. Vi&eth; leitum a&eth; einstaklingum me&eth; j&aacute;kv&aelig;tt hugarfar, g&oacute;&eth;a a&eth;l&ouml;gunarh&aelig;fni og h&aelig;fni til a&eth; takast &aacute; vi&eth; &aacute;skoranir.&nbsp;Vaktavinna er nau&eth;synleg og felur &iacute; s&eacute;r dag-, kv&ouml;ld- og n&aelig;turvaktir.
&nbsp;
H&aelig;fniskr&ouml;fur:
<ul>
<li>A&eth; l&aacute;gmarki 3 &aacute;ra reynsla &iacute; lyfjai&eth;na&eth;i.</li>
<li>G&oacute;&eth; reynsla af vinnu &iacute; A og B vottu&eth;u umhverfi.</li>
<li>Menntun: BS e&eth;a dipl&oacute;ma &iacute; t&aelig;knigreinum, (t.d. l&iacute;ft&aelig;kni, verkfr&aelig;&eth;i, l&iacute;fefnafr&aelig;&eth;i) er kostur en ekki skilyr&eth;i.</li>
<li>&THORN;ekking &aacute; g&oacute;&eth;um framlei&eth;slu h&aacute;ttum (GMP) og h&aelig;fni til a&eth; fylgja verklagsreglum vi&eth; skr&aacute;ningar.</li>
<li>H&aelig;fni til &thorn;ess a&eth; vinna vel &iacute; teymi.</li>
<li>G&oacute;&eth; enskukunn&aacute;tta.</li>
</ul>
&nbsp;
[English]
&nbsp;
Overview of Role
&nbsp;
Join the Drug Product Manufacturing Team at Alvotech in Reykjavik! Alvotech operates in a highly regulated environment that requires attention to detail and thoroughness. We're seeking someone with strong leadership skills, a positive attitude, and the ability to adapt to challenges.&nbsp;Working day, evening, and night shifts is required.
&nbsp;
Scope and responsibility:
<ul>
<li>Work in accordance with cGMP standards across various cleanroom zones (Grade A, B, C, and CNC).</li>
<li>Be part of a collaborative team working to meet the drug product (DP) manufacturing schedule.</li>
<li>Serve as a Subject Matter Expert for PAIs, audits and regulatory agency interactions.</li>
<li>Author, review and approve written procedures, SOPs, deviations, CAPAs and change controls.</li>
<li>Ensure DP manufacturing area and equipment are in inspection-ready state through interaction with Engineering, Facilities, and EHS.</li>
<li>Continuously identify opportunities for process improvement and waste elimination to maintain a lean, flexible and agile manufacturing facility. &nbsp;</li>
</ul>
Job requirements:
<ul>
<li>3+ years in (bio)pharmaceuticals is required.</li>
<li>Good experience working in grade A and B environment.</li>
<li>Education: BSc or Diploma in a Technical Discipline (e.g., biotechnology, engineering, biochemistry or related field) is advantage but not a requirement.</li>
<li>Knowledge of Good Manufacturing Practices (GMP), documentation rules, and an ability to follow the documentation for the execution of batch records, SOPs and work instructions is required.</li>
<li>Ability to work well in a team.</li>
<li>Proficient English skills, Icelandic language not required.</li>
</ul>

What we offer: 
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>

Why Alvotech : &nbsp;At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We&rsquo;re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment. True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let&rsquo;s create a healthier world together, through affordable biologic medicines.


Gakktu til liðs við framleiðsluteymi hjá Alvotech í Reykjavík!
Alvotech starfar í reglubundnu umhverfi þar sem nákvæmni og samviskusemi skipta sköpum. Við leitum að einstaklingum með jákvætt hugarfar, góða aðlögunarhæfni og hæfni til að takast á við áskoranir.
Vaktavinna er nauðsynleg og felur í sér dag-, kvöld- og næturvaktir.




Hæfniskröfur:


 - Að lágmarki 3 ára reynsla í lyfjaiðnaði.

 - Góð reynsla af vinnu í A og B vottuðu umhverfi.

 - Menntun: BS eða diplóma í tæknigreinum, (t.d. líftækni, verkfræði, lífefnafræði) er kostur en ekki skilyrði.

 - Þekking á góðum framleiðslu háttum (GMP) og hæfni til að fylgja verklagsreglum við skráningar.

 - Hæfni til þess að vinna vel í teymi.

 - Góð enskukunnátta.





[English]




Overview of Role




Join the Drug Product Manufacturing Team at Alvotech in Reykjavik! Alvotech operates in a highly regulated environment that requires attention to detail and thoroughness. We're seeking someone with strong leadership skills, a positive attitude, and the ability to adapt to challenges.
Working day, evening, and night shifts is required.




Scope and responsibility:


 - Work in accordance with cGMP standards across various cleanroom zones (Grade A, B, C, and CNC).

 - Be part of a collaborative team working to meet the drug product (DP) manufacturing schedule.

 - Serve as a Subject Matter Expert for PAIs, audits and regulatory agency interactions.

 - Author, review and approve written procedures, SOPs, deviations, CAPAs and change controls.

 - Ensure DP manufacturing area and equipment are in inspection-ready state through interaction with Engineering, Facilities, and EHS.

 - Continuously identify opportunities for process improvement and waste elimination to maintain a lean, flexible and agile manufacturing facility.




Job requirements:


 - 3+ years in (bio)pharmaceuticals is required.

 - Good experience working in grade A and B environment.

 - Education: BSc or Diploma in a Technical Discipline (e.g., biotechnology, engineering, biochemistry or related field) is advantage but not a requirement.

 - Knowledge of Good Manufacturing Practices (GMP), documentation rules, and an ability to follow the documentation for the execution of batch records, SOPs and work instructions is required.

 - Ability to work well in a team.

 - Proficient English skills, Icelandic language not required.




What we offer: 


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.




Why Alvotech :


At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.

True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together, through affordable biologic medicines.

Technician in Manufacturing Team

&Iacute;slenska&nbsp;
Alvotech leitar a&eth; Associate Scientist &iacute; frumur&aelig;ktun til a&eth; styrkja USP ranns&oacute;knar- og &thorn;r&oacute;unarteymi&eth;. Starfi&eth; felur &iacute; s&eacute;r stu&eth;ning vi&eth; &thorn;r&oacute;un frumur&aelig;ktunarferla &iacute; sm&aacute;skala l&iacute;fhv&ouml;rfum me&eth; &thorn;a&eth; a&eth; markmi&eth;i a&eth; skala upp og yfirf&aelig;ra ferla yfir &iacute; framlei&eth;slu &aacute; l&iacute;ft&aelig;knilyfjahli&eth;st&aelig;&eth;um (biosimilars)&nbsp; &nbsp; (English)&nbsp;
Alvotech is seeking a dedicated cell culture associate scientist to join our Upstream Process (USP) Research and Development (R&amp;D) team. As an associate scientist, you will play an important support role in our USP team developing a small-scale bioreactor process for subsequent scale-up and transfer to a manufacturing environment for production of biosimilars. &nbsp;
Job Description&nbsp;
Scope and responsibility: &nbsp; &nbsp;
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="32" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
General supervision and upkeep of the USP Development laboratory to ensure it remains clean and well-organized. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="33" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Responsible for managing, maintaining and stocking the specific USP Development laboratory inventory such as raw material, consumable and equipment supplies etc. Communication with vendors for purchasing and with warehouse/procurement/supply chain regarding orders and tracking. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="34" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Responsible for tracking and performing equipment regular maintenance and upkeep of logbooks. Proactively participate in authoring and updating the equipment specific procedures and work instructions. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="35" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Support USP Development scientists in sample labelling, submission, internal/external sample transport and assist in sample result tracking. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="36" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Support USP Development scientists for study preparation and/or execution such as bioreactor assembly/disassembly, daily sampling, raw material dispensing and media/feed preparation etc. &nbsp;
</li>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="37" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Proactively propose general laboratory improvements and willing to take up additional activities, as applicable. &nbsp;
</li>
</ul>
Qualifications &amp; Experience:&nbsp;
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="38" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
University degree; BSc or MSc (Preferred) within biotechnology, biochemistry, biochemical engineering or related field. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="39" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Work experience in the field of biotechnology or comparable for 1-3 years is an advantage. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="40" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Practical lab work experience and basic scientific knowledge within the field of biotechnology or comparable is an advantage. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="41" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Excellent command of the English language, both verbal and written, with the ability to communicate fluently. &nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="42" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
Scientific mindset, solution oriented, great team player with good adaptability and positive attitude. &nbsp;
</li>
</ul>
What we offer:&nbsp;&nbsp;
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="1" data-aria-level="1">
An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="2" data-aria-level="1">
The chance to be a part of a global and fast-growing company.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="3" data-aria-level="1">
An international work culture that encourages diversity, collaboration and inclusion.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="4" data-aria-level="1">
Positive, flexible, and innovative work environment.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="5" data-aria-level="1">
Support for personal growth and internal career development.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="6" data-aria-level="1">
Company social events and milestone celebrations.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="7" data-aria-level="1">
Excellent in-house canteen and coffee house.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="8" data-aria-level="1">
Exercise and wellbeing support for full-time employees.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="9" data-aria-level="1">
On-site shower facility.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="10" data-aria-level="1">
Transportation grant towards eco-friendly modes of travel for full-time employees.&nbsp;
</li>
</ul>
<ul>
<li aria-setsize="-1" data-leveltext="" data-font="Symbol" data-listid="7" data-list-defn-props="{&quot;335552541&quot;:1,&quot;335559685&quot;:720,&quot;335559991&quot;:360,&quot;469769226&quot;:&quot;Symbol&quot;,&quot;469769242&quot;:[8226],&quot;469777803&quot;:&quot;left&quot;,&quot;469777804&quot;:&quot;&quot;,&quot;469777815&quot;:&quot;multilevel&quot;}" data-aria-posinset="11" data-aria-level="1">
Internet at home for full-time employees. &nbsp;
</li>
</ul>
Why Alvotech :&nbsp; &nbsp; At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We&rsquo;re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.&nbsp;
&nbsp; True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let&rsquo;s create a healthier world together, through affordable biologic medicines.&nbsp;


Íslenska


Alvotech leitar að Associate Scientist í frumuræktun til að styrkja USP rannsóknar- og þróunarteymið. Starfið felur í sér stuðning við þróun frumuræktunarferla í smáskala lífhvörfum með það að markmiði að skala upp og yfirfæra ferla yfir í framleiðslu á líftæknilyfjahliðstæðum (biosimilars)



(English)


Alvotech is seeking a dedicated cell culture associate scientist to join our Upstream Process (USP) Research and Development (R&amp;D) team. As an associate scientist, you will play an important support role in our USP team developing a small-scale bioreactor process for subsequent scale-up and transfer to a manufacturing environment for production of biosimilars. 


Job Description


Scope and responsibility: 





 - 

General supervision and upkeep of the USP Development laboratory to ensure it remains clean and well-organized. 





 - 

Responsible for managing, maintaining and stocking the specific USP Development laboratory inventory such as raw material, consumable and equipment supplies etc. Communication with vendors for purchasing and with warehouse/procurement/supply chain regarding orders and tracking. 





 - 

Responsible for tracking and performing equipment regular maintenance and upkeep of logbooks. Proactively participate in authoring and updating the equipment specific procedures and work instructions. 





 - 

Support USP Development scientists in sample labelling, submission, internal/external sample transport and assist in sample result tracking. 





 - 

Support USP Development scientists for study preparation and/or execution such as bioreactor assembly/disassembly, daily sampling, raw material dispensing and media/feed preparation etc. 



 - 

Proactively propose general laboratory improvements and willing to take up additional activities, as applicable. 




Qualifications &amp; Experience:



 - 

University degree; BSc or MSc (Preferred) within biotechnology, biochemistry, biochemical engineering or related field. 





 - 

Work experience in the field of biotechnology or comparable for 1-3 years is an advantage. 





 - 

Practical lab work experience and basic scientific knowledge within the field of biotechnology or comparable is an advantage. 





 - 

Excellent command of the English language, both verbal and written, with the ability to communicate fluently. 





 - 

Scientific mindset, solution oriented, great team player with good adaptability and positive attitude. 




What we offer:




 - 

An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.





 - 

The chance to be a part of a global and fast-growing company.





 - 

An international work culture that encourages diversity, collaboration and inclusion.





 - 

Positive, flexible, and innovative work environment.





 - 

Support for personal growth and internal career development.





 - 

Company social events and milestone celebrations.





 - 

Excellent in-house canteen and coffee house.





 - 

Exercise and wellbeing support for full-time employees.





 - 

On-site shower facility.





 - 

Transportation grant towards eco-friendly modes of travel for full-time employees.





 - 

Internet at home for full-time employees. 




Why Alvotech :



At Alvotech, we are passionate about improving lives by increasing access to affordable biologics. We’re purpose-driven and committed to fostering an inclusive and diverse working environment that encourages curiosity, ingenuity and simplicity. We want our employees to feel inspired in their careers, challenged by interesting and meaningful work and empowered to succeed in an agile environment.




True to our Icelandic roots, we also believe that integrity, gender equality, and fairness are foundational. We strive to bring together the brightest minds regardless of backgrounds and beliefs, to deliver to our partners and patients around the world. Let’s create a healthier world together, through affordable biologic medicines.


Associate Scientist, USP Development 

Scope and Responsibilities:
<ul>
<li>Management and oversight of individual analytical method transfers for QC, including protocol/report/gap analysis generation and implementation plans, review and approval workflows between the receiving and transferring unit.&nbsp;</li>
</ul>
<ul>
<li>Participate in preparations for regulatory submissions, inspections, and responses to health authorities and/or partners for QC related activities.&nbsp;</li>
</ul>
<ul>
<li>Responsible for ensuring timely completion of individual projects and assisting with establishing and maintaining departmental metrics.&nbsp;</li>
</ul>
<ul>
<li>Independence in assignments and take part in small to medium departmental/cross-functional projects.&nbsp;</li>
</ul>
<ul>
<li>Routinely leads projects internally and with external stakeholders&nbsp;</li>
</ul>
<ul>
<li>Expert knowledge within the field of expertise such as analytical methods, techniques and equipment as well as relevant procedural/process knowledge.&nbsp;</li>
</ul>
<ul>
<li>Ability to discuss challenges and communicate business critical information to supervisor or other relevant stakeholders.&nbsp;</li>
</ul>
&nbsp;
Specifics of the role:
<ul>
<li>Execution of day-to-day activities within the QC department relating to Analytical Method Transfer, Partner requests, CMO requests and Health authority related activities.&nbsp;</li>
</ul>
<ul>
<li>Ensuring timely completion and support to Health Authority related activities, Partner requests and Analytical Method Transfers.&nbsp;</li>
</ul>
<ul>
<li>Performs both routine tasks within procedures, processes and non-routine tasks such as identifying and/or support/lead change controls, document updates, and CAPAs.&nbsp;</li>
</ul>
<ul>
<li>Management of individual Analytical Method Technology transfer/validation documentation.&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Identifying required document changes and updating of quality documentation.&nbsp;</li>
</ul>
<ul>
<li>Provide technical training and support to the team as needed.&nbsp;&nbsp;</li>
</ul>
<ul>
<li>Be aware of and comply with Alvotech&rsquo;s current EHS policies.&nbsp;</li>
</ul>
&nbsp;
Job requirements:
<ul>
<li>Education: Minimum B.S in a technical discipline, (e.g., pharmacy, biotechnology, biochemistry, or a related field)&nbsp;</li>
</ul>
<ul>
<li>Experience: 5+ years of experience in the pharmaceutical or biopharmaceutical industry.</li>
<li>Experience in quality management system, analytical method transfers, and working cross functionally with excellent communicational skills.</li>
<li>Good conceptual, problem-solving, and organizational skills &ndash; must be detail-oriented, well-organized, and able to work independently and in teams.&nbsp;</li>
<li>Fluent command of the English language, both written and verbal.</li>
</ul>
&nbsp;
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


Scope and Responsibilities:


 - Management and oversight of individual analytical method transfers for QC, including protocol/report/gap analysis generation and implementation plans, review and approval workflows between the receiving and transferring unit.




 - Participate in preparations for regulatory submissions, inspections, and responses to health authorities and/or partners for QC related activities.




 - Responsible for ensuring timely completion of individual projects and assisting with establishing and maintaining departmental metrics.




 - Independence in assignments and take part in small to medium departmental/cross-functional projects.




 - Routinely leads projects internally and with external stakeholders




 - Expert knowledge within the field of expertise such as analytical methods, techniques and equipment as well as relevant procedural/process knowledge.




 - Ability to discuss challenges and communicate business critical information to supervisor or other relevant stakeholders.






Specifics of the role:


 - Execution of day-to-day activities within the QC department relating to Analytical Method Transfer, Partner requests, CMO requests and Health authority related activities.




 - Ensuring timely completion and support to Health Authority related activities, Partner requests and Analytical Method Transfers.




 - Performs both routine tasks within procedures, processes and non-routine tasks such as identifying and/or support/lead change controls, document updates, and CAPAs.




 - Management of individual Analytical Method Technology transfer/validation documentation.





 - Identifying required document changes and updating of quality documentation.




 - Provide technical training and support to the team as needed.





 - Be aware of and comply with Alvotech’s current EHS policies.






Job requirements:


 - Education: Minimum B.S in a technical discipline, (e.g., pharmacy, biotechnology, biochemistry, or a related field)




 - Experience: 5+ years of experience in the pharmaceutical or biopharmaceutical industry.

 - Experience in quality management system, analytical method transfers, and working cross functionally with excellent communicational skills.

 - Good conceptual, problem-solving, and organizational skills – must be detail-oriented, well-organized, and able to work independently and in teams.


 - Fluent command of the English language, both written and verbal.





What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

QC Strategic Operation Lead

Gakktu til li&eth;s vi&eth; framlei&eth;sluteymi&eth; hj&aacute; Alvotech &iacute; Reykjav&iacute;k! Vi&eth; leitum a&eth; einstaklingum me&eth; j&aacute;kv&aelig;tt vi&eth;horf, g&oacute;&eth;a a&eth;l&ouml;gunarh&aelig;fni og getu til a&eth; takast &aacute; vi&eth; &aacute;skoranir.&nbsp;Vinna &aacute; dag- og kv&ouml;ldv&ouml;ktum er nau&eth;synleg.
&THORN;essi sta&eth;a b&yacute;&eth;ur upp &aacute; hagn&yacute;ta reynslu &iacute; al&thorn;j&oacute;&eth;legu umhverfi &aacute;samt fj&ouml;lbreyttum t&aelig;kif&aelig;rum til starfs&thorn;r&oacute;unar!

Helstu verkefni og &aacute;byrg&eth;:
<ul>
<li>Flutningur framlei&eth;sluefna fr&aacute; v&ouml;ruh&uacute;si yfir &iacute; Class D sv&aelig;&eth;i.</li>
<li>Fylla &aacute; og vi&eth;halda Kanban efnaherbergjum &aacute; DSM1 og DSM2 sv&aelig;&eth;um.</li>
<li>Tryggja a&eth; framlei&eth;slu&aacute;&aelig;tlun s&eacute; uppf&aelig;r&eth;.</li>
<li>Sty&eth;ja vi&eth; heildarframlei&eth;slu og tryggja a&eth; &aacute;&aelig;tlanager&eth; s&eacute; r&eacute;tt framkv&aelig;md.</li>
</ul>

H&aelig;fniskr&ouml;fur:
<ul>
<li>Grunn&thorn;ekking &aacute; vi&eth;eigandi ferlum og t&aelig;kni.</li>
<li>Fram&uacute;rskarandi samskiptah&aelig;fileikar.</li>
<li>Geta til a&eth; vinna &iacute; teymi.</li>
<li>Stundv&iacute;si og &aacute;rei&eth;anleiki.</li>
<li>Sveigjanleiki og g&oacute;&eth; a&eth;l&ouml;gunarh&aelig;fni.</li>
</ul>

[English]

Join our production team at Alvotech in Reykjav&iacute;k!
We are looking for individuals with a positive attitude, strong adaptability, and the ability to tackle challenges.&nbsp;Working day and evening shifts is required.
This position offers hands-on experience in an international environment along with diverse opportunities for professional development!

Key Responsibilities:
<ul>
<li>Material transfer of process materials from Warehouse to Class D area.</li>
<li>To stock up and maintain Kanban material rooms in DSM1 and DSM2 areas.</li>
<li>Ensure to update planning related activities.</li>
<li>To support overall manufacturing &amp; ensure planning is performed properly.</li>
</ul>

Qualifications:
<ul>
<li>Basic technical or administrative knowledge or relevant process knowledge.</li>
<li>Adhere to the company etiquette in all matters of behavior and manners.</li>
<li>Excellent communication skills.</li>
<li>Strong work ethic and proven ability to collaborate effectively in team</li>
<li>Punctual and reliable.</li>
<li>Flexible/adaptable.</li>
</ul>

What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


Gakktu til liðs við framleiðsluteymið hjá Alvotech í Reykjavík! Við leitum að einstaklingum með jákvætt viðhorf, góða aðlögunarhæfni og getu til að takast á við áskoranir.
Vinna á dag- og kvöldvöktum er nauðsynleg.

Þessi staða býður upp á hagnýta reynslu í alþjóðlegu umhverfi ásamt fjölbreyttum tækifærum til starfsþróunar!



Helstu verkefni og ábyrgð:


 - Flutningur framleiðsluefna frá vöruhúsi yfir í Class D svæði.

 - Fylla á og viðhalda Kanban efnaherbergjum á DSM1 og DSM2 svæðum.

 - Tryggja að framleiðsluáætlun sé uppfærð.

 - Styðja við heildarframleiðslu og tryggja að áætlanagerð sé rétt framkvæmd.




Hæfniskröfur:


 - Grunnþekking á viðeigandi ferlum og tækni.

 - Framúrskarandi samskiptahæfileikar.

 - Geta til að vinna í teymi.

 - Stundvísi og áreiðanleiki.

 - Sveigjanleiki og góð aðlögunarhæfni.




[English]



Join our production team at Alvotech in Reykjavík!

We are looking for individuals with a positive attitude, strong adaptability, and the ability to tackle challenges.
Working day and evening shifts is required.

This position offers hands-on experience in an international environment along with diverse opportunities for professional development!



Key Responsibilities:


 - Material transfer of process materials from Warehouse to Class D area.

 - To stock up and maintain Kanban material rooms in DSM1 and DSM2 areas.

 - Ensure to update planning related activities.

 - To support overall manufacturing &amp; ensure planning is performed properly.




Qualifications:


 - Basic technical or administrative knowledge or relevant process knowledge.

 - Adhere to the company etiquette in all matters of behavior and manners.

 - Excellent communication skills.

 - Strong work ethic and proven ability to collaborate effectively in team

 - Punctual and reliable.

 - Flexible/adaptable.




What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

Manufacturing Technologist

The Quality Control department at Alvotech is looking for a dedicated and quality-minded QC Analytical Product Testing Senior scientist with extensive experience in the field, who will be a part of the Quality control team responsible for quality control and release testing of product manufactured at Alvotech.

Scope and responsibility:
<ul>
<li>Performs routine analytical testing using advanced analytical techniques including Chromatography, Electrophoresis, Compendial and functional testing to support stability, in-process and release analysis.</li>
<li>Expertise in selected analytical techniques and through understanding and overview of all analytical methods applied for product testing and stability testing.</li>
<li>Be aware of compendia and routine testing equipment used during product testing</li>
<li>Complete laboratory documentation and records in accordance with Good Documentation Practices (GDP).</li>
<li>Proactively communicate analytical issues, deviations, and concerns to relevant stakeholders.</li>
<li>Review and verify analytical data and test results.</li>
<li>Support and lead CAPAs, change control, Document change controls and the investigations for quality issues such as Invalid assay, OOS/OOT/OOE results.</li>
<li>Review and approve technical documentation within the document management system, as required.</li>
<li>Provide support and oversight to other scientists in the laboratory</li>
<li>Proactively ensure the QC Analytical laboratory and equipment is at all times maintained in a state of Inspection readiness.</li>
<li>Perform training of other scientist in laboratory activities and specific methods.</li>
<li>Creates and updates documents for analytical methods</li>
</ul>
<ul>
<li>Knowledge about basic tasks in the labs and responsible for analytical methods.</li>
<li>Actively involved and contributes to cross functional activities.</li>
</ul>

Job requirements:
<ul>
<li>Minimum M.S in technical discipline, (e.g., pharmacy, biotechnology, biochemistry, or a related field)</li>
<li>5-10 years of experience in Pharmaceutical or Biopharmaceutical industry and preferably a project management background/exposure.</li>
<li>Good conceptual, problem solving, and organizational skills &ndash; must be detail-oriented and able to work independently and in teams</li>
<li>Independence in assignments. Routinely leads projects and/or supervises small or medium teams. Additionally takes part in larger projects.</li>
<li>Expert knowledge within field of expertise such as methods, techniques as well as relevant procedural/process knowledge</li>
<li>Open to flexible working hours.</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
&nbsp;
What we offer:
<ul>
<li>An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.</li>
<li>The chance to be a part of a global and fast-growing company.</li>
<li>An international work culture that encourages diversity, collaboration and inclusion.</li>
<li>Positive, flexible, and innovative work environment.</li>
<li>Support for personal growth and internal career development.</li>
<li>Company social events and milestone celebrations.</li>
<li>Excellent in-house canteen and coffee house.</li>
<li>Exercise and wellbeing support for full-time employees.</li>
<li>On-site shower facility.</li>
<li>Transportation grant towards eco-friendly modes of travel for full-time employees.</li>
<li>Internet at home for full-time employees.</li>
</ul>
About Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.
&nbsp;
We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.
&nbsp;
Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.

If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.

If you have any technical issues, please contact: hr@alvotech.com


The Quality Control department at Alvotech is looking for a dedicated and quality-minded QC Analytical Product Testing Senior scientist with extensive experience in the field, who will be a part of the Quality control team responsible for quality control and release testing of product manufactured at Alvotech.



Scope and responsibility:


 - Performs routine analytical testing using advanced analytical techniques including Chromatography, Electrophoresis, Compendial and functional testing to support stability, in-process and release analysis.

 - Expertise in selected analytical techniques and through understanding and overview of all analytical methods applied for product testing and stability testing.

 - Be aware of compendia and routine testing equipment used during product testing

 - Complete laboratory documentation and records in accordance with Good Documentation Practices (GDP).

 - Proactively communicate analytical issues, deviations, and concerns to relevant stakeholders.

 - Review and verify analytical data and test results.

 - Support and lead CAPAs, change control, Document change controls and the investigations for quality issues such as Invalid assay, OOS/OOT/OOE results.

 - Review and approve technical documentation within the document management system, as required.

 - Provide support and oversight to other scientists in the laboratory

 - Proactively ensure the QC Analytical laboratory and equipment is at all times maintained in a state of Inspection readiness.

 - Perform training of other scientist in laboratory activities and specific methods.

 - Creates and updates documents for analytical methods



 - Knowledge about basic tasks in the labs and responsible for analytical methods.

 - Actively involved and contributes to cross functional activities.




Job requirements:


 - Minimum M.S in technical discipline, (e.g., pharmacy, biotechnology, biochemistry, or a related field)

 - 5-10 years of experience in Pharmaceutical or Biopharmaceutical industry and preferably a project management background/exposure.

 - Good conceptual, problem solving, and organizational skills – must be detail-oriented and able to work independently and in teams

 - Independence in assignments. Routinely leads projects and/or supervises small or medium teams. Additionally takes part in larger projects.

 - Expert knowledge within field of expertise such as methods, techniques as well as relevant procedural/process knowledge

 - Open to flexible working hours.

 - Excellent written and verbal communication skills.





What we offer:


 - An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.

 - The chance to be a part of a global and fast-growing company.

 - An international work culture that encourages diversity, collaboration and inclusion.

 - Positive, flexible, and innovative work environment.

 - Support for personal growth and internal career development.

 - Company social events and milestone celebrations.

 - Excellent in-house canteen and coffee house.

 - Exercise and wellbeing support for full-time employees.

 - On-site shower facility.

 - Transportation grant towards eco-friendly modes of travel for full-time employees.

 - Internet at home for full-time employees.


About Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.




We offer a dynamic, fast-moving environment where curiosity, initiative and ownership are encouraged. Rooted in Icelandic values and operating on a global stage, we value collaboration, diversity and integrity across everything we do. Our teams work on meaningful challenges, contribute directly to patient impact, and grow alongside the business.




Whether you are at the start of your career or looking to take your next step, Alvotech offers the opportunity to do work that matters, in a company driven by purpose and scale.



If you do not see a role that matches your experience today, we still welcome general applications from individuals who share our ambition and want to help improve access to biologic medicines worldwide.



If you have any technical issues, please contact: hr@alvotech.com

QC Analytical Product Testing Senior scientist

I. PMO Systems Ownership
<ul>
<li>Own and administer CapEx PMO systems, reporting platforms, and digital tools.</li>
<li>Develop and maintain the PMO systems roadmap, including enhancements, integrations, and digitalization initiatives.</li>
<li>Own the Power BI reporting environment and related analytics solutions.</li>
<li>Act as system owner and administrator for Asana and other approved PMO applications.</li>
<li>Design, develop, and maintain integrations across Power Platform, SharePoint, Workday, SAP, Microsoft Project, Asana, and other enterprise systems.</li>
</ul>

II. Solution Development &amp; Analytics
<ul>
<li>Develop applications, workflows, automations, dashboards, and reporting solutions that improve portfolio visibility and operational efficiency.</li>
<li>Lead development of resource planning, forecasting, and analytical tools supporting portfolio management.</li>
<li>Develop data models, performance metrics, and decision-support solutions.</li>
<li>Evaluate emerging technologies and identify opportunities for automation and digital transformation.</li>
</ul>

III. Business Partnership
<ul>
<li>Collaborate with project management, engineering, finance, procurement, IT, and leadership teams to understand business requirements and deliver scalable digital solutions.</li>
<li>Provide analytical insights and reporting to support portfolio planning, resource management, and capital investment decisions.</li>
<li>Support adoption, training, and continuous improvement of PMO systems and digital processes.</li>
</ul>

Minimum Education &amp; Experience
<ul>
<li>B.Sc. or M.Sc. in Computer Science, Software Engineering, Information Systems, Data Science, or a related technical discipline.</li>
<li>Minimum 5 years of experience in software development, business intelligence, system administration, systems integration, automation, data analytics, or related technical roles.</li>
<li>Proven experience developing applications, workflows, automations, dashboards, reporting solutions, and data-driven business tools.</li>
<li>Strong experience with Microsoft Power BI, Power Platform, SharePoint, Microsoft 365, and data modeling.</li>
<li>Experience integrating enterprise systems and managing data across multiple platforms.</li>
<li>Experience with Workday, SAP, Asana, Microsoft Project, or similar platforms is advantageous.</li>
<li>Ability to translate business requirements into scalable digital solutions.</li>
<li>Strong analytical, problem-solving, and stakeholder management skills.</li>
<li>Experience in a regulated pharmaceutical, biotechnology, or other GxP-regulated environment is desirable.</li>
</ul>
 BS - Computer and Information Science, BS - Software EngineeringAbout Us
At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.


I. PMO Systems Ownership


 - Own and administer CapEx PMO systems, reporting platforms, and digital tools.

 - Develop and maintain the PMO systems roadmap, including enhancements, integrations, and digitalization initiatives.

 - Own the Power BI reporting environment and related analytics solutions.

 - Act as system owner and administrator for Asana and other approved PMO applications.

 - Design, develop, and maintain integrations across Power Platform, SharePoint, Workday, SAP, Microsoft Project, Asana, and other enterprise systems.




II. Solution Development &amp; Analytics


 - Develop applications, workflows, automations, dashboards, and reporting solutions that improve portfolio visibility and operational efficiency.

 - Lead development of resource planning, forecasting, and analytical tools supporting portfolio management.

 - Develop data models, performance metrics, and decision-support solutions.

 - Evaluate emerging technologies and identify opportunities for automation and digital transformation.




III. Business Partnership


 - Collaborate with project management, engineering, finance, procurement, IT, and leadership teams to understand business requirements and deliver scalable digital solutions.

 - Provide analytical insights and reporting to support portfolio planning, resource management, and capital investment decisions.

 - Support adoption, training, and continuous improvement of PMO systems and digital processes.




Minimum Education &amp; Experience


 - B.Sc. or M.Sc. in Computer Science, Software Engineering, Information Systems, Data Science, or a related technical discipline.

 - Minimum 5 years of experience in software development, business intelligence, system administration, systems integration, automation, data analytics, or related technical roles.

 - Proven experience developing applications, workflows, automations, dashboards, reporting solutions, and data-driven business tools.

 - Strong experience with Microsoft Power BI, Power Platform, SharePoint, Microsoft 365, and data modeling.

 - Experience integrating enterprise systems and managing data across multiple platforms.

 - Experience with Workday, SAP, Asana, Microsoft Project, or similar platforms is advantageous.

 - Ability to translate business requirements into scalable digital solutions.

 - Strong analytical, problem-solving, and stakeholder management skills.

 - Experience in a regulated pharmaceutical, biotechnology, or other GxP-regulated environment is desirable.



BS - Computer and Information Science, BS - Software EngineeringAbout Us

At Alvotech, we are building a global biotechnology company with a clear purpose: to expand access to high-quality, affordable biologic medicines for patients worldwide. Our people are central to that mission. Across our global teams, we bring together expertise in science, manufacturing, quality and commercial operations to shape the future of biosimilars.