Senior Quality Assurance
Posted 2 days ago by CK Group- Science, Clinical and Technical
£29 Per hour
Inside
Hybrid
Uxbridge
Summary: CK Group is seeking a Senior Quality Assurance Specialist for a 12-month contract with a global pharmaceutical company. The role involves hybrid working, with 50% of the time spent on-site in Uxbridge, focusing on quality assurance vendor oversight and compliance with regulations. The ideal candidate will have a relevant scientific degree and experience in interacting with health authorities. This position is crucial for ensuring quality standards in pharmaceutical development and manufacturing processes.
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:
- Hold a 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/hour
City: Uxbridge
Country: UK
Working Arrangements: hybrid
IR35 Status: inside IR35
Seniority Level: Senior
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 (phone number removed) or email (url removed). 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.