QC analyst
- Schweiz
- Freiberuflich
- Vollzeit
- Job type:
Good Manufacturing Practice (GMP) * Location:
SwitzerlandNeuchâtel, SwitzerlandPosting date: 13 Aug 2025Reference: 66649Proclinical is seeking a QC Analyst to join a pharmaceutical company in Neuchatel, Switzerland, on a contract basis. In this role, you will focus on performing biochemical analyses and ensuring compliance with GMP standards within a fast-paced quality control laboratory environment. This position requires a proactive and detail-oriented individual who thrives in a dynamic setting.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:
- Conduct biochemical analyses such as ELISA, enzymatic activity assays, Western Blot, and HPLC.
- Ensure compliance with GMP, EHS, and quality control procedures.
- Document results accurately in logbooks and forms following Good Documentation Practices (ALCOA).
- Report non-conformities or invalid results promptly and initiate quality events as required.
- Manage laboratory investigations and troubleshoot minor issues within your area of expertise.
- Execute qualification protocols for reagents, consumables, methods, systems, and equipment.
- Verify calibration and maintenance of equipment before analysis.
- Maintain Kanban inventory management in real-time.
- Support continuous improvement initiatives and adhere to 5S standardization practices.
- Collaborate with supervisors and experts to address procedural deviations.
- Educational background in laboratory biology (CFC) or a relevant scientific field.
- Experience in a QC laboratory within a cGMP environment.
- Proficiency in techniques such as electrophoresis, HPLC, ELISA, or enzymatic activity determination.
- Fluency in French and technical proficiency in English.
- Swiss or EU nationality, or a valid Swiss work permit.