QC Analyst

CK QLS are recruiting for a Quality Control Analyst, to join our client who are a leading Pharmaceutical company, on a contract basis, initially for 6 months.

You bring strong laboratory experience, including biochemical methods such as HPLC, ELISA, enzyme activity, Western Blot, etc. Through your work as a laboratory technician, you have developed a good theoretical and practical understanding of biochemical methods and technology. Present your subject of expertise, deviations, and the content of change controls during Inspections.

Main Missions :

• Comply with cGMP, BPD and EHS standards.
• Carry out routine and non-routine process activities.
• Provide coaching and knowledge sharing on routine and non-routine QC activities.
• Address technical and/or organizational issues.
• Propose technical or organizational solutions.
• Solve complex technical problems.
• Propose and follow up ideas for continuous improvement.
• Initiate work orders.
• Initiate or guarantee the adequacy of initiations of deviations in the context of non-compliance in a quality system within a given time.
• Inform and raise awareness among colleagues in the production area of deviations occurring in their area.
• Ensure the correct understanding and application of the CAPAs defined in the QC zone over time.

Required Profile :

• Minimum level of studies: CFC laboratory/biology or another relevant scientific field.
• 5 years minimum experience in QC laboratory in cGMP environment.
• Experience in HPLC Electrophoresis analysis, Elisa, or in determining the desired enzymatic activity.
• Fluent French and technical English required.
• Swiss or EU nationality, or valid Swiss work permit.

Apply:

If you would like to apply for this role please contact Rob Angrave at CK QLS on rangrave@ckqls.ch or apply via the link. Please quote job reference 107274 in all correspondence.