QA Analyst

Boehringer Ingelheim GmbH; United Kingdom; A distancia; GBP 30.000 - 42.000; Jornada completa

Descripción de la vacante

The Quality Assurance Analyst at Boehringer Ingelheim UK plays a key role in ensuring batch release activities meet regulatory requirements and internal quality standards. The role focuses on review and coordination of batch documentation to support timely product release with data integrity and GMP compliance.

This fixed-term position runs until 31 December 2027 and involves cross-functional collaboration with production, supply chain, quality control and the QP to ensure accurate, compliant

Formación

• Experience with GMP and data integrity in a regulated setting.
• Familiarity with batch record review processes or QA activities.
• Proficiency with quality and business systems (LIMS, SAP).
• Strong attention to detail and ability to review technical documentation accurately.
• Excellent written and verbal communication skills.
• DBS check will be required for the successful candidate.

Responsabilidades

• Prepare and review batch documentation for QP certification and regulatory alignment.
• Perform batch review activities including production checks and formulation sheet reviews.
• Execute quality tasks within LIMS and SAP related to batch release.
• Participate in batch tracking and communicate issues to stakeholders.
• Support batch record review projects and continuous improvement initiatives.
• Manage archiving and handling of batch documentation and document control.
• Provide operational support including deviation management, investigations and change control.
• Assist with internal audits and quality system maintenance.

Conocimientos

GMP

Data integrity

LIMS

SAP

Attention to detail

Organisational skills

Communication

MS Office

Educación

Scientific degree (advantageous)

Herramientas

LIMS

SAP

Descripción del empleo

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 EudraLex 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 berequiredfor the successful candidate. Any offer of employmentwill be subject toa satisfactoryDBS certificate.

WHY THIS IS A GREAT PLACE TO WORK

Boehringer Ingelheim has been recognised as aTop 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:
https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work