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 audits (e.g., Cx, R&D QA, SOG). Own Rx audit capability and competency management, including talent identification, auditor training matrices, and development plans in collaboration with Product Supply, Network, Quality Systems, and auditors’ line managers. Establish and maintain Rx audit systems and governance, defining compliant processes, procedures, SOPs, and standard ways of working aligned with the Mundipharma Quality Framework, GxP requirements, and local regulations. Design and manage the global risk‑based Rx audit schedule, applying Quality Risk Management principles to determine audit frequency, scope, resourcing, and prioritization. Ensure audit performance, resourcing, and reporting excellence, defining metrics and dashboards to monitor effectiveness, identify improvement opportunities, and proactively escalate compliance risks. Oversee Quality Agreements, CAPAs, and issue management, ensuring findings are resolved effectively, monitored to closure, and communicated in a timely manner to protect product quality, safety, and efficacy. Support inspection readiness and regulatory compliance, acting as an auditing SME for internal and external inspections while maintaining inspection‑ready records, data integrity, and secure handling of audit documentation. Serve as a global audit advisor and collaborator, providing expert guidance on regulatory interpretation, aligning with other GxP audit groups on global standards, engaging CMOs and third parties, and driving continuous improvement and best‑practice sharing. Skills & Qualifications Education: Scientific degree in Pharmacy, Chemistry, Biology, or similar; or equivalent aligned working experience. Certification: Lead Auditor certification (or similar). What we offer in return Competitive compensation package Learning & development opportunities through structured programs A collaborative, inclusive, and values‑driven work environment Diversity and inclusion At Mundipharma, building an inclusive environment where everyone can thrive is a priority. We are committed to fostering a culture that embraces diversity, equity, and respect, enabling every employee to bring their authentic self to work every day. About Mundipharma Mundipharma is a global healthcare company serving patients across Africa, Asia Pacific, Canada, Europe, Latin America, and the Middle East. We are dedicated to delivering innovative treatments in pain management, infectious diseases, and other severe and debilitating conditions, guided by our core principles of Integrity and Patient‑Centricity. Learn more at www.mundipharma.com Join our talent pool If you’re not sure this role is right for you but you’re keen to hear about future opportunities at Mundipharma, join our talent community and be the first to hear about new roles. Additional Job Description: Primary Location: GB Cambridge Job Posting Date: 2026-03-04 Job Type: Permanent