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QA Analyst

Job in Woking, Surrey County, GU22, England, UK
Listing for: Boehringer Ingelheim
Full Time position
Listed on 2026-08-27
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager, Quality Control - QC Analysts/Managers, Data Analyst, Regulatory Compliance Specialist
Job Description & How to Apply Below
THE POSITION The Quality Assurance Analyst plays a key role in ensuring that batch release activities are performed accurately and in compliance with applicable regulatory requirements and internal quality standards. This position focuses on the review and coordination of batch documentation, supporting timely product release while maintaining high standards of data integrity and Good Manufacturing Practice (GMP). Working cross-functionally with production, supply chain, quality control and the Qualified Person (QP), the role contributes directly to the safe and efficient release of products.

This is a fixed-term contract until 31st December 2027.Tasks and Responsibilities Prepare and review batch-specific documentation to ensure completeness and accuracy prior to Qualified Person (QP) certification, in alignment with Eudra Lex Volume 4, Annex 16

Perform additional batch review activities, including production checks and formulation sheet reviews

Execute quality-related tasks within systems such as LIMS and SAP relevant to batch release processes

Participate in batch tracking activities and communicate quality-related issues to relevant stakeholders in a timely manner

Support projects and initiatives related to batch record review and process improvement

Manage archiving and handling of batch documentation, including in-process documentation control

Provide operational support in line with business needs, including:
Supporting deviation management, investigations and change control

Assisting with document control processes

Participating in internal audits and quality system maintenance

Ensure compliance with EU GMP, internal procedures, and applicable regulatory and biosafety requirements

Requirements

Understanding of Good Manufacturing Practice (GMP) principles and data integrity requirements

Experience working in a quality system environment within a regulated industry (e.g. pharmaceutical or biologics manufacturing) is advantageous

Familiarity with batch record review processes or similar quality assurance activities is preferred

Ability to work with quality and business systems (e.g. LIMS, SAP or equivalent)
Strong attention to detail and ability to review technical documentation accurately

Well-developed organisational and prioritisation skills, with the ability to manage multiple tasks in a dynamic environment

Effective communication skills, both written and verbal, with the ability to collaborate across functions and with different stakeholders

Proactive and solution-oriented mindset with a collaborative approach to problem-solving

Basic proficiency in Microsoft Office tools (e.g. Excel, PowerPoint, Outlook)
A degree or educational background in a scientific or related field would be advantageous

Please note:

a Disclosure and Barring Service (DBS) check will be required for the successful candidate. Any offer of employment will be subject to a satisfactory DBS certificate.

WHY THIS IS A GREAT PLACE TO WORKBoehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies.

To learn more about why BI is a great place to work, visit:
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