QA Manager

QA, Quality, GMP, QMS, Audit, CAPA, Gene, Therapy, Cell, Biotech

Your new company
This company is an American Biotech company based in Stevenage. They are a clinical-stage immuno-oncology company developing the next generation of novel T cell therapies for patients suffering from cancer. They have recently embarked on establishing GMP manufacturing operations in the UK and their aim is to provide manufacturing capacity for Phase 1 & Phase 2 operations and beyond.

Your new role
With a strong pipeline in 2020 and rapid expansion across their UK operations, they are looking to invest in their quality team through the permanent appointment of a QA Manager. Your role will be to lead the manufacturing and release of products under the GMP QMS, support product and batch record reviews, investigations into non-compliances, CAPA management, supplier qualification and documentation controls. You will be responsible for the preparation of manufacturing batch records for final review and QP lot release and review Change Control records impacting T cell therapy product. As QA Manager, you also be responsible for recruiting and developing the Quality team.

What you'll need to succeed
In order to be considered for this position you will have minimum of 10 years GMP experience in a biotech, or biologics operation. Experience with QMS, audit and various GMP QA activities is necessary. T Cell therapy experience is desirable however not necessary.

What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.


Job type:
Working Pattern
Quality Assurance and Validation
Apply Now

Talk to a consultant

Talk to Chandni Pankhania, the specialist consultant managing this position, located in London City

4th Floor, 107 Cheapside

Telephone: 02034650133

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