

QC Bioassay Associate Scientist
Við leitum að metnaðarfullum og nákvæmum sérfræðingi í gæðastýringu (QC Bioassay Associate Scientist) til að styðja við gæðaprófanir á líftæknilyfjum. Starfið felur í sér framkvæmd og bilanagreiningu lífefnafræðilegra mælinga, eftirlit að farið sé eftir reglugerðum og gæðastöðlum auk þess að taka þátt í umbótaverkefnum innan QC.
(English)
About the Role
We are seeking a motivated and detail‑oriented QC Bioassay Associate Scientist to support quality control testing activities for biologics. This role is responsible for executing and troubleshooting bioanalytical assays, ensuring compliance with regulatory standards, and contributing to continuous improvement initiatives within the QC laboratory.
Key Responsibility:
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Perform routine and non-routine bioassays (e.g., cell-based potency assays, ELISA, binding assays) in compliance with GMP requirements
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Analyze, interpret, and document experimental data in line with ALCOA+ data integrity standards
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Support cell culture activities, including preparation of master and working cell banks, microscopy, and aseptic techniques
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Prepare testing protocols and reports, and review laboratory and cell bank documentation
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Assist in laboratory operations, including buffer/media preparation, stock checks, cleaning, and equipment upkeep
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Perform analytical data collection and ensure accurate, compliant documentation of results
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Support qualification and optimization of critical reagents (e.g., reference materials) and technical troubleshooting
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Maintain compliance with GMP and EHS policies, and contribute to quality documentation updates and improvements
Qualifications & Experience
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Bachelor’s or Master’s degree in Biochemistry, Biotechnology, Biology, or a related field
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Typically 1-1.5 years of experience in a laboratory is preferred.
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Excellent documentation, organizational, and communication skills
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Ability to work both independently and collaboratively in a fast-paced environment
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Communication skills: Excellent written and verbal communication skills
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Computer literacy: Proficient in use of a PC and common Microsoft packages such as Word, Excel
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Organisation and management skills: Will be required to participate and make positive contribution to team meetings. Responsible for individual performance management.
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GMP & GDP experience: Will be expected to work to and comply with the requirements of Alvotech QMS cGMP and GDP Practises and Policies. Will participate in self inspections and regulatory inspections.
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Attention to detail and precise work habits.
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Initiative to suggest process and environment improvements to managers and colleagues as appropriate.
What we offer
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An inspiring challenge to work with great co-workers on ambitious projects that change people's lives.
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The chance to be a part of a global and fast-growing company.
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An international work culture that encourages diversity, collaboration, and inclusion.
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Positive, flexible, and innovative work environment.
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Support for personal growth and internal career development.
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Company social events and milestone celebrations.
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Excellent in-house canteen and coffee house.
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Exercise and well-being support for full-time employees.
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On-site shower facility.
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Transportation grant towards eco-friendly modes of travel for full-time employees.
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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.
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