A growing organisation within the molecular imaging space is seeking a Senior Quality Manager to lead oversight of EU and Rest-of-World (RoW) manufacturing partners and supply chain quality.
This is a high-impact role focused on ensuring compliant, uninterrupted supply of specialised medicinal products across international markets.
Key Responsibilities
- Lead quality oversight of EU/RoW Contract Manufacturing Organisations (CMOs)
- Manage manufacturing performance, investigations, and quality issue resolution
- Own and execute a risk-based audit programme
- Drive quality governance, including deviations, complaints, CAPAs, and change control
- Analyse performance data to identify risks and enable continuous improvement
- Support and enhance the Quality Management System (QMS)
- Monitor regulatory developments and ensure ongoing compliance
- Collaborate cross-functionally to maintain a robust global supply chain
Requirements
- Strong experience within EU GMP environments (sterile and/or radiopharmaceuticals preferred)
- Proven experience managing CMOs or external manufacturing partners
- Background in GxP inspections and auditing
- Solid understanding of QMS (deviation, CAPA, change control, risk management)
- Ability to interpret and act on quality and operational data
- Willingness to travel (~30% across EU with occasional international travel)
We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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