QA Officer - Batch Release & QMS
Location: Runcorn
Hours: 7:00am - 3:00pm / 3:00pm - 11:00pm (rotating) Monday to Friday
Salary: Competitive + Shift Allowance + Annual Bonus
We are seeking 2Â highly motivated QA Officers to join our client's Quality team in Runcorn. This role offers the opportunity to split your time between batch release activities and Quality Management System (QMS) support, helping to maintain the highest standards of product quality and regulatory compliance.
Key Responsibilities
• Review and approve batch documentation to ensure compliance with specifications and GMP.
• Assess and approve batches for release to market or internal use.
• Support investigations of deviations and non-conformities, ensuring effective resolution and compliance.
• Manage QMS activities including complaints, events, CAPA and change control.
• Compile Certificates of Conformance and support KPI reporting.
• Review and update SOPs, worksheets and QC specification documents.
• Provide QA support to QC-led projects and continuous improvement initiatives.
• Deputise for the QC Shift Team Leader where required.
About You
• Degree in a Life Science subject (or equivalent experience).
• At least 3 years' experience in QA/QC within pharmaceutical manufacturing.
• Strong working knowledge of GMP and QMS processes.
• Excellent attention to detail and strong organisational skills.
• A collaborative team player who can also work independently.
What's On Offer
• Competitive salary plus shift allowance and annual bonus.
• Opportunity to gain exposure across QA and QC functions.
• A supportive environment focused on continuous improvement and development.
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Back to searchQA Officer - Batch Release and QMS
Russell Taylor Group Ltd
Posted 9 days ago, valid for 20 days
Runcorn, Cheshire WA7 1BE, England
£28,000 - £33,600 per annum
Full Time
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Sonic Summary
- We are looking for 2 motivated QA Officers to join a Quality team in Runcorn, focusing on batch release and Quality Management System (QMS) support.
- The role requires at least 3 years of experience in QA/QC within pharmaceutical manufacturing and offers a competitive salary plus shift allowance and annual bonus.
- Key responsibilities include reviewing batch documentation, assessing batches for market release, and managing QMS activities such as complaints and CAPA.
- Candidates should possess a degree in a Life Science subject or equivalent experience, along with strong knowledge of GMP and QMS processes.
- The position provides an opportunity for professional development in a supportive environment focused on continuous improvement.
