Als neue Jobbenachrichtigung einrichten
Als neue Jobbenachrichtigung einrichten
Geben Sie nachstehend Ihre E-Mail-Adresse ein, um Benachrichtigungen in Ihrem Posteingang zu erhalten, wenn ähnliche Stellenangebote vorliegen.
Indem Sie nachstehend auf „Ja, senden Sie mir Stellenangebote zu“ klicken, stimmen Sie zu, gemäß unserer Datenschutzrichtlinie Stellenangebote auf Basis der von Ihnen gewählten Suchkriterien in Ihrem Posteingang zu erhalten.
Indem Sie nachstehend auf „Ja, senden Sie mir Stellenangebote zu“ klicken, stimmen Sie zu, gemäß unserer Datenschutzrichtlinie Stellenangebote auf Basis der von Ihnen gewählten Suchkriterien in Ihrem Posteingang zu erhalten.
Vielen Dank für Ihre Registrierung zur Jobbenachrichtigung
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.
I manage this role