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.
To be considered you must have the right to work in Switzerland 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.
Questions or difficulties applying? Contact Enile De Beer at e.debeer@proclinical.com.
Apply now by clicking "Apply" or request a call back at the top of this page.
#J-18808-Ljbffr