THE POSITION This newly created, site-based role at Pirbright is responsible for overseeing all production compliance activities across the manufacturing facility. The position ensures timely, cost-effective production of FMD and BTV antigens and finished products, fully aligned with EU, UK, and company GMP, biosafety, and HSE regulations. TASKS & RESPONSIBILITIES Production Compliance - Lead and manage the Production GMP Compliance team - Oversee departmental deviations, CAPAs, change controls, SOPs, MBRs, and training, ensuring timely closure aligned with KPIs - Conduct and lead investigations with high technical competence - Develop and manage Production Compliance KPIs - Maintain training records, OJT programs, and data integrity standards Operational Management - Ensure departmental efficiency and regulatory compliance - Support and deputise for the Head of Production - Continuously improve compliance processes, equipment, and training - Collaborate with senior colleagues to resolve inefficiencies and implement improvements - Collect and act on KPI data to reduce product wastage - Strengthen relationships with internal and external stakeholders, especially Quality Assurance and Boehringer's network colleagues Area Management - Plan and implement process improvements via change control - Manage team schedules and provide cover during absences - Coach and train staff, promoting cross-area collaboration - Oversee training budgets and contribute to annual budget planning - Participate in the production call-out rota and ensure batch close-out within 12 weeks Continuous Improvement - Lead and participate in daily Tier Meetings - Drive key improvement projects and support cross-functional initiatives Biosafety & EHS - Ensure adherence to biosafety protocols and communicate effectively - Report and investigate EHS incidents, collaborating with EHS teams - Conduct and document risk assessments - Complete required Health & Safety training Finance & Systems - Monitor training cost centre budgets and report discrepancies - Approve invoices and manage stock movements in SAP/GBS - Plan stock usage and raise orders via WeBuy GMP & Audits - Lead production readiness for internal and external audits - Act as SME during audit front-room activities - Manage change controls, deviations, CAPAs, and OOS reports - Approve and enter data in LIMS REQUIREMENTS - Degree in a biological discipline preferred; relevant experience considered - Strong time management, organisational, and leadership skills - In-depth knowledge of HSE, biosafety, GMP, and operational excellence - Proven autonomy and teamwork capabilities - Experience in regulated environments desirable - Innovative mindset with strong communication skills - Proficient in Microsoft Office - Demonstrates Accountability, Agility & Intrapreneurship (AAI) behaviours WHY THIS IS A GREAT PLACE TO WORK Boehringer Ingelheim has been recognised as a Top Employer in the UK. Being certified as a Top Employer confirms our dedication to a better world of work, delivered through excellent HR policies and people practices. To learn more visit: https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work All qualified applicants will receive consideration for employment without regard to a person's actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status, marital status; gender, gender identity or expression; sexual orientation, mental, physical or intellectual disability, veteran status; pregnancy, childbirth or related medical condition; genetic information (including the refusal to submit to genetic testing) or any other class or characteristic protected by applicable law.