Im currently looking for a QA Associate to join a Manufacturing and Drug Development business based in Berkshire. As the QA Associate you will be responsible for
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QA Associate will be to ensure that operations are compliant with internal procedures and regulatory requirements, as well as the following responsibilities:
Review and approval of analytical and manufacturing documentation prior to QP certification and involved with Batch Release processes.
Writing, reviewing and approving SOPs and writing Technical Agreements.
Participate in change control processes, ensuring changes to systems, equipment and facilities are suitably assessed and implemented.
Perform audits to monitor compliance of internal operations and procedure, including regulatory requirements.
To be successful in your application to this fantastic opportunity as the QA Associate, we are looking to identify an existing QA professional with GMP experience, as well as the following:
1. Experienced within the Pharmaceutical industry
2. Proven industry experience within a pharmaceutical GMP environment.
3. A working knowledge and practical experience within a Quality Assurance position
Key Words: QA, Quality Assurance, QA Associate, Quality Assurance Associate, GMP, Pharmaceutical, Manufacturing
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.