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16436en
- Contract
- English, French
- Associate
- Research & Development
- Neuchâtel
- Healthcare & Life Sciences
Skills
GMP, Pharma, Recombinant Therapeutic Products, Laboratory Skills, QC
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This vacancy has now expired
On behalf of our client, a global leader in the pharmaceutical industry, Swisslinx is seeking a QC Associate Scientist to support critical analytical assay activities at their site in Neuchâtel. This is an exciting opportunity for a detail-oriented professional to contribute to life cycle management, validation, and daily quality control activities in a cGMP environment.
Contract Type: Contract
Start Date: ASAP
Location: Neuchâtel, Switzerland
Workload: 100%
Duration: 12 months
Your Mission:
Life Cycle Management Activities:
• Manage analytical assay activities within QC laboratories, focusing on:
• Laboratory investigations.
• Critical material qualification.
• Laboratory method transfers.
• Support daily QC activities following cGMP, company policies, and EHS requirements.
Validation and Qualification:
• Author transfer protocols and qualification plans/reports for assays and critical reagents.
• Oversee validation and qualification activities executed by analysts, providing training and support.
• Execute and document experiments.
Investigation Leadership:
• Investigate and troubleshoot laboratory issues to identify solutions or recommend changes.
• Conduct and participate in risk assessments, root cause analyses, and investigations.
• Own laboratory investigations and implement corrective and preventive actions (CAPAs).
Quality Control Support:
• Apply compliance standards and regulations to assay life cycle management activities.
• Provide technical and statistical support for daily QC activities as needed.
Your Background:
Experience:
• University or engineering degree in analytical chemistry, biotechnology, biochemistry, or microbiology.
• Fluent in French and English (C1 level written and spoken)
• 1–2 years of experience in GMP pharma activities, preferably in recombinant therapeutic products.
• Proficiency in GMP laboratory activities, method transfers, and critical reagent qualification.
• Experience in problem-solving, deviation management, and statistical tools.
• Proficiency with standard IT tools.
Competencies:
• Strong collaboration and teamwork mindset.
• Excellent troubleshooting and problem-solving skills.
• Ability to work independently in a fast-paced environment and manage multiple priorities.
• Effective communicator with the ability to synthesize information and provide feedback.
What’s on Offer:
• A 12-month contract with a leading global pharmaceutical company.
• The opportunity to play a vital role in the life cycle management of critical assays.
• A chance to expand your expertise in laboratory investigations, validation, and quality control.
If this sounds like you, don’t hesitate to apply here or contact Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
Contract Type: Contract
Start Date: ASAP
Location: Neuchâtel, Switzerland
Workload: 100%
Duration: 12 months
Your Mission:
Life Cycle Management Activities:
• Manage analytical assay activities within QC laboratories, focusing on:
• Laboratory investigations.
• Critical material qualification.
• Laboratory method transfers.
• Support daily QC activities following cGMP, company policies, and EHS requirements.
Validation and Qualification:
• Author transfer protocols and qualification plans/reports for assays and critical reagents.
• Oversee validation and qualification activities executed by analysts, providing training and support.
• Execute and document experiments.
Investigation Leadership:
• Investigate and troubleshoot laboratory issues to identify solutions or recommend changes.
• Conduct and participate in risk assessments, root cause analyses, and investigations.
• Own laboratory investigations and implement corrective and preventive actions (CAPAs).
Quality Control Support:
• Apply compliance standards and regulations to assay life cycle management activities.
• Provide technical and statistical support for daily QC activities as needed.
Your Background:
Experience:
• University or engineering degree in analytical chemistry, biotechnology, biochemistry, or microbiology.
• Fluent in French and English (C1 level written and spoken)
• 1–2 years of experience in GMP pharma activities, preferably in recombinant therapeutic products.
• Proficiency in GMP laboratory activities, method transfers, and critical reagent qualification.
• Experience in problem-solving, deviation management, and statistical tools.
• Proficiency with standard IT tools.
Competencies:
• Strong collaboration and teamwork mindset.
• Excellent troubleshooting and problem-solving skills.
• Ability to work independently in a fast-paced environment and manage multiple priorities.
• Effective communicator with the ability to synthesize information and provide feedback.
What’s on Offer:
• A 12-month contract with a leading global pharmaceutical company.
• The opportunity to play a vital role in the life cycle management of critical assays.
• A chance to expand your expertise in laboratory investigations, validation, and quality control.
If this sounds like you, don’t hesitate to apply here or contact Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
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