Framleiðslutæknir - DPVI Technologist

Við leitum að áhugasömum einstaklingi til að ganga til liðs við eitt af teymunum okkar í framleiðslunni. Starfið felst í sjónrænni gæðaskoðun á fullbúnu lyfi 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).
  
  

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.
  
  

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.