Quality Manager (Lab Ops / GMP)

About the role

As the first dedicated Quality Manager at Phagos, you will bridge high‑speed innovation with rigorous regulatory compliance. You will design and implement a Quality Management System (QMS) that supports increased production and ensures the new GMP lab meets global veterinary medicine standards.

Key responsibilities

• Design, implement and maintain a robust QMS compliant with biotech and pharmaceutical guidelines.
• Lead the internal audit programme across all operational areas.
• Oversee qualification and auditing of suppliers and subcontractors.
• Develop and deliver training on documentation standards and quality procedures.
• Lead quality aspects of GMP lab setup, including site qualification, equipment validation and cleanroom procedures.
• Support preparation of regulatory dossiers from a quality and GMP perspective.
• Ensure defensible batch release procedures for all products.
• Lead post‑incident quality reviews and drive continuous improvement.
• Participate early in product and process development to raise quality issues proactively.

Required profile

• Degree in Pharmacy, Biology, Biotechnology or a related life‑science discipline.
• 3‑4 years of experience in a quality role within a regulated biotech, pharma or veterinary‑medicine environment.
• Comfortable with ambiguity, proactive under pressure and able to translate complex regulations into clear actions.
• Fluent English.

Required skills

• Solid working knowledge of GMP guidelines.
• Familiarity with veterinary medicinal product regulations.
• Proficiency in designing and managing QMS software and documentation.

What we offer

• International, diverse team focused on impactful biotechnology.
• Opportunity to lead processes that directly contribute to innovative biotechnologies.
• Growth and learning in a fast‑paced environment.
• Well‑being perks such as free breakfast, sports activities and a healthy work‑life balance.