Senior Quality Assurance Specialist
Posted 2 days ago by CK Group
£29 Per hour
Undetermined
Hybrid
Uxbridge, England, United Kingdom
Summary: CK Group is seeking a Senior Quality Assurance Specialist for a 12-month contract with a global pharmaceutical company. The role involves managing quality assurance activities and vendor oversight, with a hybrid working arrangement based in Uxbridge. Candidates should possess a relevant scientific degree or equivalent experience, along with in-depth knowledge of cGMP/GDP regulations. Direct experience with Health Authorities and external manufacturers is also required.
Key Responsibilities:
- Responsible for QA vendor oversight
- Manage contractor quality assurance activities
- Identify and recommend quality-related improvements
- Manage change control requests
- Review batch records
- Support GMP/GDP site inspections
Key Skills:
- Relevant scientific degree or equivalent working experience
- In-depth knowledge of cGMP / GDP regulations pertinent to the USA, EU, and other international markets
- Ability to build relationships, partnerships, and influence stakeholders
- Direct experience interacting with Health Authorities and supporting Health Authority inspections, specifically FDA and/or EMA
- Experience in interacting with external manufacturers and supporting quality at external manufacturing sites
Salary (Rate): £29 hourly
City: Uxbridge
Country: United Kingdom
Working Arrangements: hybrid
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
CK Group are recruiting for a Senior Quality Assurance Specialist to join a global pharmaceutical company on a contract basis for 12 months. This role is hybrid with 50% of time spent on site in Uxbridge.
Salary: £29 ph PAYE
Quality Assurance Specialist Role:
- Responsible for QA vendor oversight
- Manage contractor quality assurance activities
- Identify and recommend quality-related improvements
- Manage change control requests.
- Review batch records
- Support GMP/GDP site inspections
Your Background :
- Hold a relevant scientific degree or have equivalent working experience
- In-depth knowledge of cGMP / GDP regulations pertinent to the USA, EU and other international markets
- Ability to build relationships, partnerships and influence stakeholders
- Direct experience interacting with Health Authorities and supporting Health Authority inspections, specifically FDA and/or EMA
- Experience in interacting with external manufacturers and supporting quality at external manufacturing sites
Company:
Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.
Apply:
For more information, or to apply for this Quality Assurance Specialist please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@ckagroup.co.uk. Please quote reference 1744 835 . It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.