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.