Overview
Join a dynamic and innovation-driven pharmaceutical environment in Visp as a QC Scientist, where you will play a key role in ensuring the quality and reliability of analytical methods.
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
* Experience: Data Review experience is important!
* PhD in a relevant field (biotechnology, biochemistry, pharmaceuticals, etc.), then 1 year of experience desired (no experience acceptable if necessary) or MSc in a relevant field, then at least 2 years of experience desired (whether in a laboratory or as a scientist or similar)
* 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
Details
Remote: 2 days max.
Language: English mandatory / German a plus
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