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QA Specialist

GMP, QA, Quality, QMS. audit

Your new company
This company is an international and one of the world’s powerful Biotechnology companies headquartered in US. They were founded in late 1980’s and have rapidly expanded since, they now have over 10,000 employees and have strong growth and pipeline plans for 2020. Their area of expertise is the discovery, development and commercialization for various therapies treating cancer and various diseases through gene products.

Your new role
This is an initial 12 months contract as Senior QA Specialist, you will be responsible for managing the quality compliance activities to ensure product is manufactured, packaged and distributed in line with GMP/GDP regulatory guidelines. Other activities include CAPA, deviation and SOP management, as well as batch record review and documentation review.

What you'll need to succeed
Educated to BSc level in a scientific subject
GMP Quality experience
CAPA, Deviation and SOP experience
Batch release and Batch documentation experience

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.

Summary

Job type:
Temporary
Working Pattern
Full-time
Industry
Pharmaceuticals
Location
Uxbridge
Specialism
Quality Assurance and Validation
Pay
33ph
Ref:
3768844
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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