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...

ROLE SUMMARY The GSC Market Logistics individual contributor is operationally accountable for Market Logistics activities in the Irish market leading and directing team members in each of those. The incumbent coordinates material movement between dock, warehouse and first paying customer locations with the goal of creating superior customer experience in a financially viable operation in pursuit of our purpose. The GSC Market Logistics role performs activities in planning & controlling the efficient flow of product, materials, or services from the point of in-country arrival through supply chain endpoint, meeting customer requirements. Accountable that product arrives within acceptable parameters, ensuring that time objectives are achieved within existing financial constraints to meet associated targets and goals of both GSC and business partners. Accountable for the execution and continuous improvement of standard Market Logistics processes & systems, building...

GxP Audit and Inspection Director 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 uphold the highest standards of quality, compliance, and patient safety. We challenge ourselves constantly to deliver more for patients, healthcare professionals, our partners, and our employees. The Team The role will strategically lead and coordinate the global GxP audit and inspection readiness program, ensuring sustained compliance with international regulatory standards across all Good Practice domains. You will drive proactive inspection preparedness, orchestrate cross‑functional audit activities, and embed a culture of continuous improvement within quality systems. This role ensures alignment of global teams on inspection strategy, robust documentation and data integrity, and operational excellence through risk‑based compliance oversight and regulatory intelligence. Role...

Global Pricing & Tender Lead Location: Can be open on location in areas such as UK, Spain, Netherlands, Germany and Switzerland Department: Pricing & Market Access 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 This role will join the Pricing & Market Access team in driving Mundipharma’s pricing and tendering analytics & capabilities. This critical role shapes Mundipharma’s asset strategies and influences the commercial success of its portfolio. The role involves developing and implementing pricing and tendering analytics and insights capabilities, as well as establishing a value-based pricing & tendering approach and stakeholder engagement that reflect the value of...

Rx Central Quality Auditor (Process Owner) Location: Remote Department: Global Quality (Rx) Reports to: Director, Global Quality Systems 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 constantly challenge ourselves to deliver more for patients, healthcare professionals, our partners, and our employees, while operating with integrity and a strong patient‑centric culture. Role Summary Develop and lead the Rx Central Quality Auditor community, serving as the Rx audit process owner to enable risk‑based, compliant GMDP audits across CMOs, third parties, and internal manufacturing and supply chain organizations.   Responsibilities Lead and govern the Rx auditor community, ensuring effective scheduling and execution of GMDP audits across CMOs, third parties, and internal manufacturing and supply chain organizations, including support for cross‑functional...

Role Summary Responsibilities : You will take a leading role across a variety of Market Access projects, working alongside project teams to ensure that work is delivered to an exceptionally high standard Salary : £50,000 per annum Benefits : Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous holiday allowance, private medical insurance, critical illness cover, income protection, full funding for external training and more Role Type : Full-time, permanent Start Date : The role will ideally commence in May, June or July 2026, and you will be asked to state your availability on your application form Application Deadlines : Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role will close when a suitable candidate is found Location : This role is available in our  Global Headquarters in Cambridge , as well as our London office About the Role We’re...

Please note we have a separate job advert for candidates interested in joining our Value and Access or Evidence Development teams, which you can find here: Costello Medical - Current Openings . Please apply for one role at a time because assessment processes differ. Role Summary Responsibilities : You will work on medical communications projects that involve the detailed analysis and presentation of data from clinical trials, which are instrumental to the successful uptake of novel therapies  Salary : £39,000 per annum Benefits : Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous holiday allowance, private medical insurance, critical illness cover, income protection, full funding for external training, and more Role Type : Full-time, permanent Start Date : We are currently recruiting for start dates throughout 2026, and you will be asked to state your availability on your application form Application...