QC Analytical Scientist

About the role

Alvotech is seeking a QC Analytical Scientist to join its Quality Control Product Testing team. The role supports release testing of biopharmaceutical products and contributes to maintaining high quality standards throughout manufacturing.

Key responsibilities

• Perform routine analytical testing using advanced LC (APAC, SEC, CEX, N‑glycan, peptide mapping) and CE (CE‑SDS, CIEF) techniques as well as compendial methods.
• Support manufacturing operations by preparing buffers, cleaning equipment, and maintaining laboratory stock.
• Participate in creation, review, and maintenance of quality documents and assist with change control, CAPA, and document change processes.
• Investigate quality issues such as invalid assays, OOS/OOT/OOE results and contribute to root‑cause analysis.

Required profile

• Bachelor’s or Master’s degree in a relevant scientific discipline.
• 1–5 years of experience in the pharmaceutical or biopharmaceutical sector.
• Proficiency with PC and Microsoft Word/Excel.
• Ability to review electronic data from instrument software.
• Knowledge of Good Manufacturing Practices (GMP) is an asset.

Required skills

• LC techniques (APAC, SEC, CEX, N‑glycan, peptide mapping).
• CE techniques (CE‑SDS, CIEF).
• Microsoft Word and Excel.
• PC operation and electronic instrument data analysis.
• Understanding of GMP documentation requirements.

What we offer

• Opportunity to work on ambitious projects that impact patients’ lives.
• International, diverse, and inclusive work culture.
• Support for personal growth and internal career development.
• Company social events, milestone celebrations, and an excellent in‑house canteen.
• Well‑being programs, on‑site shower facilities, and transportation grants for eco‑friendly travel.