Ph3Experteer Overview /h3pIn this role, you lead GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities across the Global Supply Chain. You’ll evaluate site conformity to GMP, policies, and regulatory commitments, covering internal and external networks, LOCs, RD, and LSPs. You’ll provide sterile manufacturing expertise to the EMEA auditing team and drive clear audit reporting with corrective action plans. You’ll work with senior stakeholders to navigate complex audits and risk‑based findings. This is a high‑impact chance to strengthen quality and regulatory compliance at scale. /ph3Retribuzione / Benefits /h3ulliManage complex stakeholder engagement for audits across the network (Site Directors, Site Quality Directors, VPs/Heads of support functions, RD Quality) /liliPerform audits of Global Supply Chain sites, LOCs, external manufacturing sites, LSPs and facilities supplying EMEA and other markets /liliConduct unannounced audits /liliConduct for‑cause audits based on regulatory actions or identified risk /liliPerform process‑and‑quality‑system‑specific audits and targeted audits /liliAudit against risk mitigation plans or regulatory citation commitments /liliProduce clear, concise audit reports and drive corrective action plans with senior management /liliTravel to sites across the network (up to ~40%) /liliLocation flexibility to be based at Ware, Worthing, Barnard Castle, Siena, Parma, Wavre, Rixensart or Tres Cantos /li /ulh3Responsabilità /h3ulliDegree in a relevant Scientific, Technical or Engineering discipline /liliRelevant experience in Steriles/Biopharm/Vaccines/Pharmaceutical industries /liliSubject matter knowledge of world‑wide cGMPs, regulatory requirements and Quality Management Systems for Steriles/Biopharm/Vaccines/Pharmaceutical Manufacturing and Packing /liliExperience identifying or managing complex Quality and Compliance risks and issues /li /ulh3Requisiti fondamentali /h3ulliannual bonus /lililong term incentive program /li /ul /p #J-18808-Ljbffr