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 for a contract role of 1 year (with potential extension), based in 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
Seniority Level
Not Applicable
Employment Type
Contract
Job Function
Science
Industries
Pharmaceutical Manufacturing
#J-18808-Ljbffr