
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.

QC Testing/Gæðarannsóknardeild - Scientist
A scientist in the Quality Control 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
Helstu verkefni og ábyrgð
- Performs routine analytical testing with advanced analytical techniques such as Liquid chromatography (SEC, APAC, CEX, etc..) and Capillary electrophoresis (iCIEF, CE-SDS) as well as compendial methods (colour, clarity, subvisible particles, TOC, etc..) and review of analytical test records to support manufacturing operations.
- Performing routine cleaning, verification, stock checks and upkeep of laboratory and equipment
- Performing activities required to support testing, e.g. buffer preparation
- Will be required to participate and make positive contributions to team meetings.
- Participate in the creation and maintenance of quality documents within Alvotech.
- Contributes to other documentational review and/or updates within the Quality management system.
- Knowledgeable about the production procedures of the different products manufactured by Alvotech
- Trains simple tasks, methods and review.
- Completes lab records review according to GDP rules.
- Proactively ensure the QC Analytical laboratory and associated documents is at all times maintained in a state of Inspection readiness.
- Supports deviations, CAPAs, document change controls and Change controls
- Supports laboratory investigations
- Be able to work in accordance with GMP practices, conducting all activities in a compliant manner
- Be aware of and comply with Alvotech’s current EHS policies
Fríðindi í starfi
- Knowledge of Good Manufacturing Practices (GMP) and documentation Rules is an asset.
- Ability to work on a shift-based pattern work schedule
- Proficient in the use of a PC and common Microsoft packages such as Word and Excel.
- Understanding and review of electronic data from instrument software.
- Bachelor´s Degree in a relevant scientific discipline and a minimum of 1-5 years of relevant experience in the pharmaceutical or biopharmaceutical sector.
Utworzono ofertę pracy24. July 2025
Termin nadsyłania podań14. August 2025
Znajomość języków

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Lokalizacja
Sæmundargata 15-19 15R, 101 Reykjavík
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