We are seeking an experienced and highly skilled Qualified Person (QP) to join our client based in the Southeast of England. This is a full-time, permanent position offering an excellent opportunity to play a key role in ensuring the quality and safety of medicinal products.
Key Requirements
- Overseeing the batch certification of sterile medicinal products, ensuring full compliance with regulations.
- Reviewing and approving batch records, analytical data, and associated documentation.
- Investigating and resolving quality issues and deviations.
- Participating in audits (both internal and external) to uphold high standards in quality systems.
- Providing expert advice on regulatory requirements and quality standards.
Ideal candidate
- Previous involvement as a releasing QP within sterile products
- Experience managing a Quality Management System (QMS).
- A robust background in pharmaceutical manufacturing and quality assurance.
- A qualification in a scientific discipline (e.g., pharmacy, chemistry, or biology).
- Completion of the educational requirements for QP certification
This role is fully site-based and does not offer remote working.