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Quality Control Associate (M/F/D)
Tasks:
- Ability to perform and approve QC lab analyses in strict compliance with SOPs
- Skilled in problem-solving and troubleshooting (basic and complex issues)
- Competence in training analysts and acting as a GMP trainer backup
- Strong ownership and attention to detail in lab and documentation tasks
- Ability to manage deviations, investigate root causes, and propose CAPAs
- Proactive in EHS compliance and reporting non-conformities
- Experience participating in inspections/audits and presenting technical topics
- Collaboration across internal and external stakeholders (suppliers, subcontractors)
- Involvement in continuous improvement, 5S, GEMBA, and HOP initiatives
- Effective communication and teamwork, with patient-oriented mindset
Qualification:
- Minimum CFC in microbiology or equivalent experience in the pharmaceutical or biotech industry
- 2–5 years’ experience in a cGMP laboratory or at least 2 years as Analyst I
- At least 5 years’ experience in a cGMP laboratory or at least 5 years as Analyst II
- Good laboratory method knowledge
- Very strong laboratory method knowledge
- Good knowledge of cGMP
- Understanding of Data Integrity
- Strong knowledge of Data Integrity principles
Requirements:
Start: asap
Duration: 28.02.2026
Capacity: 5 days per week
Location: Neuchatel, Switzerland
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