Proclinical 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.

Key Skills and Requirements:

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.

If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.

Apply Now:

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