Ensure precision and compliance-drive quality control excellence as our QC Scientist in Switzerland.
Proclinical is seeking a QC Scientist for a contract role based in Switzerland. This position focuses on quality control within the cardiovascular and contract manufacturing sectors. The role involves method development, validation, and troubleshooting in a laboratory setting. Candidates with expertise in ELISA methods, relative potency, and qPCR are highly encouraged to apply.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Manage project tasks related to method development, implementation, transfer, and validation.
- Draft test instructions, methods, plans, and reports.
- Review and release raw data and analysis results in LIMS.
- Provide specialist support for laboratory troubleshooting.
- Handle CRs, DRs, investigations, SST, OOX, and CAPAs.
- Plan, execute, evaluate, and document assigned tasks and projects independently.
- Ensure compliance with ISO, GMP, and safety standards.
Key Skills and Requirements:
- Experience in data review is essential.
- Hands-on experience with ELISA methods, relative potency, and qPCR.
- Background in GMP environments is advantageous.
- PhD in biotechnology, biochemistry, pharmaceuticals, or a related field (experience preferred but not mandatory), or MSc with relevant laboratory or scientific experience.
- Proficiency in English is required; German is a plus.
- Ability to work remotely up to 2 days per week.