QC Scientists – Analytical (Shift & Daytime Roles)

Við leitum að tveimur sérfræðingum (Scientist) til að ganga til liðs við Quality Control Product Testing teymið hjá Alvotech. Þessar stöður gegna lykilhlutverki í gæðaeftirliti og losun afurða sem framleiddar eru hjá Alvotech. Stöðurnar eru innan Analytical starfseiningarinnar og styðja við framleiðslu með háþróuðum greiningaraprófunum og gæðaskjölun.

(English below)

We are looking for two Scientists to join the Quality Control Product Testing team at Alvotech. These positions play a vital role in ensuring the quality control and release of products manufactured at Alvotech. The roles are within the Analytical function, supporting manufacturing operations through advanced analytical testing and quality documentation.

The two Scientist positions available are:

• Scientist – Shift Work (24/7 operations)

• Scientist – Daytime Work

Both roles involve similar responsibilities, with work schedules adapted to either a shift‑based or standard daytime working pattern.

Scope and responsibilities:

• Perform routine analytical testing using advanced analytical techniques such as LC (APAC, SEC, CEX, N-glycan, Peptide mapping) and CE (CE-SDS, CIEF), as well as compendial methods, in support of manufacturing operations.

• Participate in the creation, review, and maintenance of quality documents within Alvotech.

• Contribute to documentation reviews and updates within the Quality Management System.

• Support investigations related to quality issues, including Invalid assay, OOS/OOT/OOE results.

• Support change controls, CAPAs, and document change controls.

• Perform both routine tasks within established procedures and non-routine tasks such as investigation support, document updates, and CAPAs.

• Carry out routine cleaning, verification, stock checks, and general upkeep of laboratory areas and equipment.

• Perform activities required to support testing, e.g. buffer preparation.

Job requirements:

• Bachelor’s or Master’s degree in a relevant scientific discipline.

• 1–5 years of relevant experience in the pharmaceutical or biopharmaceutical industry.

• Proficient in using a PC and common Microsoft tools such as Word and Excel.

• Experience with understanding and reviewing electronic data from instrument software.

• Knowledge of Good Manufacturing Practices (GMP) and documentation rules is an asset.

• Ability to work a shift-based schedule is required for the 24/7 shift position.

• Ability to work standard daytime hours is required for the daytime 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 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.

Why Alvotech

We at Alvotech 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.