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    1. Home
    2. Industrial Placements
    3. Pharmaceuticals & Science
    4. Production Compliance Placement 2025
    Lock Applications for this job are now closed
    Closing soon

    These are 12-month internship opportunities starting in September 2025.  They are fully site-based roles requiring 5 days per week in Pirbright. 

    The role

    • Conduct investigations into issues that arise within Production and assess how these might affect the compliance of manufacturing.
    •  Learn how to drive and maintain the adherence to Production compliance by supporting investigation and write up of Quality records.
    • With the Compliance team, Provide compliance support to production areas.
    • Assist with writing and review of process documents.
    • Collaborate with the Quality department to support audits / inspections and collate and provide information as required.
    • Gain an understanding of Production process by embedding within the departments.
    • Obtain and maintain aseptic gowning qualified status to ensure access to all Production areas.

    Requirements

    • Applicants will be studying for a BSc Biology, Chemistry, Biochemistry or other Biological Sciences degree.
    • 3 A levels at grade BBC (minimum) with at least one grade coming from a scientific subject.
    • Applicants must have the ability for independent travel to work and other sites.
    • Applicants must be able to comply with bio-safety regulations that apply to working in a SAPO4 facility.
    • Applicants must have the right to work in the UK.
    • Ability to work independently and autonomously to drive completion of actions as well as within a team environment.
    • Excellent attention to detail.
    • Ability to work accurately in a busy and demanding environment.
    • First class organisational skills, with the ability to prioritise. 
    • Able to manage time effectively, being able to plan and complete work to schedule.

    Why us?

    • Through this placement you will gain the following benefits.
    • Broad spectrum of processes required for pharmaceutical / scientific manufacturing.
    • Deep understanding of the compliance requirements in manufacturing.
    • On the job exposure to Quality systems and their importance.
    • Working within a matrix organisation.
    • Opportunity to influence the continuous improvement of the site.
    • The ability to investigate, write up and close compliance records.
    • How to respond to complex problems.
    • How to manage conflicting priorities.