Downstream Process Engineer – GMP Biologics
Job in
6000, Luzern, Kanton Luzern, Switzerland
Listed on 2026-09-01
Listing for:
CK QLS
Full Time, Contract
position Listed on 2026-09-01
Job specializations:
-
Pharmaceutical
Pharmaceutical Manufacturing, Regulatory Compliance Specialist
Job Description & How to Apply Below
Location: Luzern
CK QLS is seeking an Associate Specialist in Downstream Operations for a 12-month, full-time on-site role in the greater Lucerne area. The position focuses on supporting GMP manufacturing of early-stage therapies, with responsibilities spanning setup, execution, and documentation of downstream processes.
The candidate should have 1–2 years of pharma/biotech experience, strong problem-solving skills, and fluent German (C1) and English (B2+). Relocation to Schachen vicinity is welcomed.
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