Are you an experienced Quality Assurance Officer looking for an exciting new challenge to help shape the QA Department of a contract pharmaceutical manufacturing organisation?
Job Title: Quality Assurance Officer
Type: Permanent
Salary: Highly attractive with great benefits
Location: Northwest, England
SRG is currently working exclusively with a highly successful, award winning, contract development and manufacturing organisation, focused on providing expert intelligence and support to their partners, driven by their capabilities.
As a result of expansion into a new state of the art facility, we are looking for a Quality Assurance Officer to join their quality team and be a key member of the QA function.
Typical responsibilities/accountabilities:
- Manage documentation through the documents lifecycle, ensuring compliance with regulations and industry best practices.
- Creating, reviewing, and approving key documentation such as specifications, SOPs, protocols, and methods associated with a product.
- QA review and dossier collation of GMP production and analytical documentation prior to QP release.
- Investigating and addressing deviations to prevent future occurrences.
- Managing supplier suitability and any issues and supplier mitigation steps for supplier complaints raised.
- Proactively able to identify and manage site improvements for Quality Improvement through CAPAs.
- Ensure training on procedures (SOPs) is up-to-date and in line with industry standards. Prepare and conduct quality training sessions, including induction and GMP training.
Essential Requirements:
- Minimum of 1 years' experience in Quality Assurance within a Pharmaceutical (GMP) facility, preferably Investigational Medicinal Products (IMPs).
- Degree in a relevant scientific discipline desired.
- Experience in working with analytical laboratories and GMP production areas.
- An understanding of GMP and regulatory requirements within the pharmaceutical industry.