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:

Duration : 28.02.2026