For our international pharma client we are looking for a
Scientist QC (m/f/d).
Workload: 100%
Location: Visp
Home office: 2 days per week max
Duration: 12 months (possibility of extension)
Responsibilities:
Responsible for project tasks in the area of method development, implementation, transfer and validation
Writing test instructions, methods, plans and reports
Double check and release raw data and analysis results in LIMS
Specialist support for the laboratory (troubleshooting)
Processing of CRs, DRs, investigations (SST, OOX, etc.) and CAPAs
Independent planning, implementation, evaluation and documentation of the assigned tasks and projects
Compliance with quality (ISO and GMP) and safety standards
Requirements
Data review experience is important
PhD in a relevant field (biotechnology, biochemistry, pharmaceuticals, etc.) with 1 year of experience desired (no experience acceptable if necessary)
MSc in a relevant field with at least 2 years of experience desired (laboratory or scientist roles)
Focus on ELISA methods (relative potency)
Focus on qPCR
Hands‑on laboratory experience and/or validation/development of these methods
GMP experience is a plus
English mandatory