Alvotech hf

Alvotech er fjölþjóðlegt hátæknifyrirtæki í fremstu röð, þar sem yfir 1000 starfsmenn af um 64 þjóðernum vinna að því að móta framtíðina á sviði líftæknilyfja og auka aðgengi sjúklinga um allan heim að hágæða lyfjum. Margir af færustu vísindamönnum landsins starfa hjá fyrirtækinu. 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 allra starfsmanna, 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.

Vinnustaðurinn

Senior Laboratory Specialist

Quality Control is looking for a laboratory specialist to support day-to-day operation on three different laboratories. Within the scope of the role is driving and supporting installation, qualification and maintenance of laboratory equipment's, inventory management, 5S tasks and general support to the testing unit in QC

Helstu verkefni og ábyrgð

Oversight of all QC laboratories within the Quality Control reporting to QC Laboratory manager.
Be responsible for all GMP compliance aspects of the labs, including equipment, employees, supplies, and documentation.
Be responsible for the safe and efficient running of the Quality Control laboratory infrastructure.
Review and approve generated technical documentation within the document management system.
Partake in installation and qualification of equipment.
Maintain regulatory readiness, participate actively in regulatory preparation and inspections.
Provide oversight and technical guidance, ensuring an optimal level of scientific ability and training within the department.
Identify required document changes and empower staff to implement changes promptly.

Menntunar- og hæfniskröfur

Minimum B.S in a technical discipline, (e.g., pharmacy, biotechnology, biochemistry, engineering, or a related field)
3+ years of experience in pharmaceutical industry.
Experience in quality management system, installation and qualification of laboratory equipment and other health authority requirements for GMP laboratories.
Good conceptual, problem-solving, and organizational skills – must be detail-oriented, well-organized, and able to work independently and in teams.

Fríðindi í starfi

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.