SRG - QA Manager

Job Title:
QA Manager
Technical roles
Closing Date:

Job Title: QA Manager
Duration: Permanent
Salary: competitive
Location: West Yorkshire

•Maintain an effective pharmaceutical quality system in line with FDA CRF 21, EU GMP, GDP, GLP and relevant ICH guidelines, ensuring the site remains inspection ready at all times
•Manage a team of QA staff to ensure timely batch release of internally manufactured batches
•Manage the quality of third party products
•Provide senior compliance support to all departments with respect to GxP requirements
•Review and approval of documentation and input to investigations
•Provide mentoring and guidance to team, development and appraisals

•BSc or equivalent in Chemistry or related subject 
•Experience of leading a team within Pharmaceutical quality, experience of continuous improvement is highly desirable
•Understanding of GxP within a pharmaceutical environment and awareness EU GMP, ICH Guidelines and FDA CRF 21
•Highly competent in report writing and experience in third part auditing

SRG are the UK number 1 recruitment company specialising in the science, engineering, clinical, pharmaceutical, food/FMCG, renewable, biotech, chemicals and medical devices sectors.

As scientists ourselves, our specialist sector knowledge and our passion are second to none. It’s this combination that makes us different. We’re committed to providing outstanding temporary, contract and permanent career opportunities of all levels for our candidates and a comprehensive range of expert strategic recruitment services for our clients.

If you would like to apply for this position, please use the link provided. Alternatively please email a copy of your CV to Daniel Nightingale at For more information regarding this position or any others, please call Dan on 0161 868 2205. 
If you have a scientific background and this position is not relevant / suitable for you please feel free to get in touch or visit to view our other vacancies. 

Keywords: GMP, Good Manufacturing Practice, Batch Release, FDA CRF 21, EU GMP, ICH Guideline, SOP, Standard Operating Procedure, Quality Assurance, QA Manager, Quality Assurance Manager, QMS, Quality Management System, GCP, GDP, GLP, Documentation

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