I’m currently looking for a QA Associate with extensive experience within Validation to join a leading Gene Therapy business based in North London. As the QA Associate, you will be responsible for the following validation and qualification activities across manufacturing and laboratory environments.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Associate will be varied however the key duties and responsibilities are as follows:
1.Review and approve tech transfer, validation and qualification protocols and reports.
2.Support the generation of Process Validation, Analytical Method Validation and equipment installation and validation, reviewing and approving reports and protocols.
3.Maintain and stay up to date regarding GMP and engineering practices in relation to all aspects of validation across manufacturing and analytical laboratories.
4.Provide QA support for data integrity activities across the site.
To be successful in your application to this exciting opportunity as the QA Associate we are looking to identify the following on your profile and past history:
1. Relevant degree within a Life Science or Pharmaceutical discipline.
2. Proven industry experience within a QA Validation position.
3. A working knowledge and practical experience of GMP environments.
Key Words: Quality, Validation, Qualification, GMP, Pharmaceutical, Quality Assurance, Gene Therapy, ATMP
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.
Employment Type: Permanent