Quality assurance analyst Work, Jobs in New Romney, Ken (with Salaries)

QA Analyst
BI AH UK Ltd —Ash
- Full-time
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook

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Quality Control Analyst (Pharmaceutical GMP)
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Working within our Quality Control laboratory, you'll support the manufacture of our GMP-grade cannabidiol (CBD) Active Pharmaceutical Ingredient (API) by…
£29,000 a year
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9d
Quality Assurance Officer (Pharmaceutical GMP)
BSPG Laboratories Ltd. —Sandwich
Working closely with Production, QC and the wider business, you'll help ensure our products are manufactured and released to the highest GMP standards.
£29,000 - £35,000 a year
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QA Analyst

BI AH UK Ltd -
Ash

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Job details

Full-time

Qualifications

Microsoft Powerpoint
Microsoft Excel
Microsoft Outlook
Microsoft Office
Quality assurance
Organisational skills
Communication skills

Full job description

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 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

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)

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 WORK

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

Apply Now

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