Job Reference: J5634562
Updated On: 04/03/2021
Status: Open to Applications
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Role OverviewI'm currently looking for a Senior Quality Assurance Associate to join a leading Cell therapy business based in the Hertfordshire area. This is a fantastic opportunity and a great time to join this exciting and innovative business.
As the Senior Quality Assurance Associate you will be responsible for the following:
Key Duties and ResponsibilitiesKEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior QA Associate will be varied however the key duties and responsibilities will be as follows:
Release documents and labels to the manufacturing production teams.
Review Change control records impacting cell therapy products
Write, review and revise quality SOP’s and associated documentation to support GMP Production.
Provide and assist in providing training for GMP and GDP processes.
Role RequirementsROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Senior QA Associate we are looking to identify the following on your profile and past history:
1. Knowledge of Quality Management System with experience of maintaining and improving systems supporting the QMS.
2. A working knowledge and practical experience of working within a Sterile environment
3. GMP experience in a biotech, or biologics operation.
Key Words: GMP, ATMP, FDA, MHRA, Quality Assurance, QA
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development. We therefore welcome applications for any interested parties who fulfil the role requirements for this position. HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists. We look forward to helping you with your next career moves.
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