Job Description

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THE POSITION

We are looking for someone to support document control activities within our Production department. In this role, you will help ensure all documentation is accurate, up to date, and easily accessible, enabling projects to run smoothly and efficiently.



This is a 3?month contract, based at our manufacturing site in Pirbright, Surrey, and requires five days per week onsite.


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TASKS & RESPONSIBILITIES

Maintain and update GMP documentation, ensuring full compliance with production standards and regulatory requirements. Draft, review, and revise SOPs and other controlled documents to reflect current procedures. Monitor and report on production compliance metrics. Build strong working relationships with internal teams, particularly Quality Assurance. Support initiatives that enhance production processes, methods, and equipment.
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REQUIREMENTS

Degree in Biology, Chemistry, Biochemistry, or another relevant Biological Science discipline. Able to read, understand, and follow detailed instructions with accuracy. Strong time management skills, with the ability to plan and prioritise workload effectively. Comfortable working independently as well as collaboratively within a wider team. Methodical, careful, and able to work with minimal supervision. Experience in a similar role or in a highly regulated environment is desirable but not essential. Strong verbal and written communication skills. A positive, proactive, "can do" approach. Confident using Microsoft Office applications.
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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