I'm currently looking for a Senior QA Associate to join a leading Pharmaceutical Development company based in Hertfordshire for a 12 month Fixed Term Contract. The business are going through exceptional growth at the moment and this role could very likely move into a permanent position.
As the Senior QA Associate, you will be responsible for the following:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior QA Associate will be varied however the key duties and responsibilities are as follows:
1.Ensure that the data Integrity and the integrity of production processes and Quality Management Systems are to the required GMP regulations.
2.You will assist with preparation and support for audits, by both clients and regulatory authorities, as well as conducting Internal Audits as required.
3.Perform periodic reviews of Quality Systems, including Deviations and Vendors.
4.Support the Vendor Management process, including carrying out Vendor Qualifications; Audits and Vendor Reviews.
To be successful in your application to this exciting opportunity as the Senior QA Associate, I'm looking to identify the following on your profile and past history:
1. Relevant degree within a Science or Pharmaceutical discipline.
2. Proven industry experience within a Pharmaceutical GMP environment.
3. A working knowledge and practical experience of working with Quality Management Systems.
Key Words: QA, Quality Assurance, QMS, Quality Management System, FTC, Fixed Term Contract, GMP, Pharmaceutical, Life Sciences, API