Alvotech hf
Alvotech hf
Alvotech hf

QC Incoming Material Scientist

We are seeking a Scientist to join our Quality Control Incoming Material Testing team. This role is essential in ensuring that all raw and incoming materials meet regulatory and internal standards before entering the manufacturing process.

You will work in a highly regulated environment that demands attention to detail, thoroughness, and a commitment to quality. We are looking for someone with a positive attitude, who embraces challenges, is flexible and adaptive, and shares our values of team spirit and collaboration.

Helstu verkefni og ábyrgð
  • Performs analytical testing of raw and incoming GxP materials used in the manufacturing process at Alvotech, with various techniques such as compendial methods, FTIR etc.
  • Performs visual inspection of product filled syringes
  • Performs visual inspection of incoming materials and goods
  • Review and interpretation of test results in compliance with pharmacopeial standards and internal procedures, following GDP standards.
  • Support verification, validation and troubleshooting of analytical techniques
  • Performing routine cleaning, verification, stock checks and upkeep of laboratory and equipment
  • Performing other activities required to support testing, e.g. solution preparation.
  • Participate and make positive contributions to team meetings.
  • Participate in the creation, maintenance and review of quality documents within the Quality management system.
  • Proactively ensure the QC Incoming Material testing laboratory is maintained in a state of Inspection readiness.
  • Supports deviations, CAPAs, document change controls and Change controls relating to incoming material testing
  • Supports laboratory investigations
  • Be able to work in accordance with GxP practices, conducting all activities in a compliant manner.
  • Responsible for adhering to all relevant Alvotech policies and procedures.
Menntunar- og hæfniskröfur
  • Bachelor´s or Master’s Degree in a relevant scientific discipline (e.g., chemistry, biotechnology, biochemistry, pharmaceutical sciences or related field) and preferably relevant experience in pharmaceutical or biopharmaceutical sector.
  • Attention to detail, thoroughness, and willingness to learn is a desired attribute.
  • Proficient in use of a PC and common Microsoft packages such as Word and Excel.
  • Understanding and review of electronic data from instrument software.
  • Knowledge of Good Manufacturing Practices (GMP) and Documentation Rules is an asset.
  • Ability to work with flexibility in a changing and demanding environment.
  • Ability to work under pressure within tight deadlines and solving issues as they arrive with minimal supervision.
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.
Auglýsing birt28. ágúst 2025
Umsóknarfrestur7. september 2025
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Staðsetning
Sæmundargata 15-19 15R, 101 Reykjavík
Starfstegund
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