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)
About Planet Pharma:
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.
Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.
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.
www.planet-pharma.com
Please click ‘apply’ or contact Finlay Keyworth (Recruiter II) at Planet Pharma for more information:
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