Analytical Chemist, Analytical Services Location: Cambridge Department: Quality Job type: Permanent Join us and make a difference when it matters most! At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. The Team This role sits within the Analytical Services section of the Quality Department laboratories. The team provides high-quality scientific and analytical expertise across a variety of pharmaceutical dosage forms, supporting product lifecycle management, continuous improvement initiatives, and global competitiveness. You will collaborate closely with cross-functional teams to ensure analytical excellence, regulatory compliance and timely project delivery. Role and Responsibilities Provide high-quality scientific and analytical expertise for a range of pharmaceutical dosage forms....

R&D QA Manager - GVP Location: Cambridge, Flexible Hybrid Department: Quality Assurance Job type: Full Time Join us and make a difference when it matters most!  At Mundipharma, we are proud of the work we do to bring innovative treatments to patients. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees.  The Team The R&D QA Manager will join the Quality Assurance team at Mundipharma and take a lead role in our Pharmacovigilance (PV) quality oversight. In this critical position, you will act as a guardian of patient safety and regulatory compliance. You will play a pivotal role in vendor management, the integrity of the Pharmacovigilance System Master File (PSMF), and supporting the wider business through high-level regulatory inspections. Role and Responsibilities Audit planning and maintenance of the R&D Audit Schedule Lead the...

ASE-S1-05 Rx Central Quality Auditor (Process Owner) Location: Remote Department: Global Quality (Rx) Reports to: Director, Global Quality Systems Job Purpose Develop and lead the Rx Central Quality Auditor community for the scheduling and execution of GMDP audits of CMOs and other third parties that are centrally managed, as well as internal manufacturing and supply chain organizations. Act as the Rx audit process owner—establishing and maintaining systems, standards, and metrics that enable effective, risk-based management of auditing activities across Mundipharma in accordance with current legislation, relevant standards and guidelines. Provide expert advice to internal and external customers, collaborate across auditing groups to define global standards and ways of working, and drive the sharing of best practices. Key Responsibilities Personnel Build and lead the auditor community for Rx, ensuring effective scheduling and execution of GMDP audits of...

Are you an ambitious Technical Manager with COMAH experience? Do you have a solid background in chemical manufacturing where you have led formulation development (NPD) and / or quality? We're a sub-contract and own label manufacturer. Our Technical Director is on course to retire. Come and spend time with them before they leave and develop yourself into their role! BASIC SALARY: Up to £60,000 BENEFITS: 25 days annual leave + bank holidays 4% company pension 3 x death in service Christmas shut-down Bonus LOCATION: Peterborough COMMUTABLE LOCATIONS: Huntingdon, Cambridge, St Neots, Bedford, Corby, Wellingborough, Kettering, Leicester, Stamford, Grantham, Spalding, Kings Lynn, March, Wisbech Why you should join us: 1. Guaranteed succession plan and growth opportunity with our Technical Director retiring 2. We are a 3rd party and own label manufacturer - so there will be so much variety and NPD 3. Ultimately full autonomy for all technical and...