Job Description

THE POSITION

Join our Production Compliance team in Pirbright and contribute to maintaining high standards of quality and GMP compliance across manufacturing operations. This role offers the opportunity to lead deviation investigations, drive CAPA and change control activities, deliver compliance training, and support continuous improvement initiatives across production departments. This is a fixed-term contract providing broad exposure to quality systems, manufacturing, and EHS and biosafety activities while working closely with cross-functional teams in a regulated biopharmaceutical environment.

The position is offered on a fixed-term basis until December 2027. Due to the nature of the production and manufacturing environment, this role requires regular onsite presence at our Pirbright, Surrey manufacturing site, with a minimum of three days per week worked onsite.

Tasks & responsibilities

• Lead deviation, CAPA, and change control activities, ensuring investigations are completed on time, root causes are identified, and effective actions are implemented.
• Provide compliance support to production teams, acting as a subject matter expert on QMS requirements and promoting consistent GMP compliance across departments.
• Identify and implement process improvements through the change control system, delivering measurable improvements to compliance, efficiency, or operational performance.
• Develop and deliver compliance training and support documentation, ensuring personnel remain trained, competent, and audit-ready.
• Collaborate with QA and cross-functional teams to support audits, respond to compliance enquiries, and maintain accurate controlled documentation.
• Drive continuous improvement, EHS compliance, and risk management activities by investigating incidents, completing risk assessments, and ensuring agreed actions are delivered within target timescales.

Requirements

• Demonstrate strong knowledge of GMP, quality systems, investigations, CAPA, and regulatory requirements within a highly regulated manufacturing environment.
• Apply scientific knowledge and practical experience gained in aseptic manufacturing, ideally involving biological products; a relevant science degree or equivalent experience is preferred.
• Build effective relationships with production, QA, and other stakeholders to support compliance and operational objectives.
• Manage multiple priorities independently, delivering accurate, high-quality work to agreed timelines in a fast-paced environment.
• Communicate clearly through concise written reports, investigations, training materials, and verbal interactions with cross-functional teams.
• Use Microsoft Office applications confidently and demonstrate a proactive, accountable approach to continuous improvement and problem solving.

WHY THIS IS A GREAT PLACE TO WORK

Boehringer Ingelheim is recognised as a Top Employer in the UK, reflecting our commitment to exceptional workplace standards, career development and a purpose-driven culture. Our employees contribute to meaningful work, creating long-term value for people, animals and the environment. Learn more about why BI is a great place to work:

https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work

Candidates may be asked to undergo a Basic Disclosure and Barring Service (DBS) Security check. Any offer of employment will be subject to satisfactory DBS certificate.