QC Scientist – 6769 ADA
Our client, a global market leader in the production and process support of active pharmaceutical ingredients, both in the chemical and biotechnology sectors, is looking for a QC Scientist a contract role of 1 year (with potential extension), based in the Visp, Switzerland.
Main 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
Qualifications and Experience:
Relevant working/residency permit or Swiss/EU-Citizenship required
PhD in a relevant field (biotechnology, biochemistry, pharmaceuticals, etc.), then 1 year of experience desired (no experience is also acceptable if other things are matching) or MSc in a relevant field, then at least 2 years of experience is desired (whether in a laboratory or as a scientist or similar)
Data Review experience is important.
Focus on ELISA methods ( relative potency ) and qPCR – hands‑on experience in the laboratory and/or in their validation/development, GMP experience also a plus
Language: English mandatory, German a plus
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