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16393en
- Contract
- English, French
- Associate
- Research & Development
- Neuchâtel
- Healthcare & Life Sciences
On behalf of our client, an international biopharmaceutical company, Swisslinx is looking for a Quality Control Analyst. In this role, you will apply your laboratory expertise in biochemical methods like ELISA and Western Blot to ensure high-quality standards in a fast-paced, team-oriented environment, while contributing to continuous improvement and compliance with GMP in the pharmaceutical industry.
Contract type - Contract
Start Date - ASAP
Location - Neuchatel
Workload - 100%
Duration - 11 months
Your Mission:
• Perform biochemical analysis and supervision activities according to the laboratory’s current procedures, complying with GMP/GDP rules and/or projects related to the Quality Control department's activities.
• Adhere to all current procedures.
• Follow and apply EHS (Environment, Health, and Safety) rules.
• Accurately complete various forms, logbooks, and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA+ principles.
• Inform the Supervisor on the same day in case of non-conforming and/or invalid results, either verbally or in writing, and initiate the quality event in the quality system within the specified timeframe.
• Manage laboratory investigations.
• Follow planning requests and proactively report any issues.
• Execute qualification protocols for reagents/consumables and validation (methods, systems, equipment).
• Ensure equipment calibration and maintenance are up to date during analysis.
• Maintain real-time Kanban management.
• Report procedural deviations to the method/equipment manager and Supervisor/Delegate/Expert.
• Identify and resolve minor issues within your area of expertise (troubleshooting).
• Prepare solutions or approve solutions in the laboratory.
• Manage and organise the laboratory, adhering to 5S standardisation norms.
• Support continuous improvement initiatives.
Your Background:
• Minimum education level: CFC laboratory technician in biology or another relevant scientific field.
• At least 3 years of experience in a QC laboratory within a cGMP environment.
• Experience in electrophoresis analysis, HPLC, ELISA, or enzymatic activity determination is desirable.
• Fluent in French and proficient in technical English.
• Swiss or EU nationality, or a valid Swiss work permit.
What's on offer
• A 11 month contract.
• A chance to develop your career at an internationally known biotechnology company.
• A competitive salary.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: hugo.palejowski@swisslinx.com.
Contract type - Contract
Start Date - ASAP
Location - Neuchatel
Workload - 100%
Duration - 11 months
Your Mission:
• Perform biochemical analysis and supervision activities according to the laboratory’s current procedures, complying with GMP/GDP rules and/or projects related to the Quality Control department's activities.
• Adhere to all current procedures.
• Follow and apply EHS (Environment, Health, and Safety) rules.
• Accurately complete various forms, logbooks, and documents in compliance with Good Manufacturing and Documentation Practices and ALCOA+ principles.
• Inform the Supervisor on the same day in case of non-conforming and/or invalid results, either verbally or in writing, and initiate the quality event in the quality system within the specified timeframe.
• Manage laboratory investigations.
• Follow planning requests and proactively report any issues.
• Execute qualification protocols for reagents/consumables and validation (methods, systems, equipment).
• Ensure equipment calibration and maintenance are up to date during analysis.
• Maintain real-time Kanban management.
• Report procedural deviations to the method/equipment manager and Supervisor/Delegate/Expert.
• Identify and resolve minor issues within your area of expertise (troubleshooting).
• Prepare solutions or approve solutions in the laboratory.
• Manage and organise the laboratory, adhering to 5S standardisation norms.
• Support continuous improvement initiatives.
Your Background:
• Minimum education level: CFC laboratory technician in biology or another relevant scientific field.
• At least 3 years of experience in a QC laboratory within a cGMP environment.
• Experience in electrophoresis analysis, HPLC, ELISA, or enzymatic activity determination is desirable.
• Fluent in French and proficient in technical English.
• Swiss or EU nationality, or a valid Swiss work permit.
What's on offer
• A 11 month contract.
• A chance to develop your career at an internationally known biotechnology company.
• A competitive salary.
If this sounds like you, don’t hesitate to apply here or reach out directly to Hugo Palejowski, Recruiter: hugo.palejowski@swisslinx.com.
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