I am working with a Pharmaceutical Manufacturing company in Slough who are looking for an Associate Principal QA Specialist to join their team on an initial 12 month contract.
• 5–10 years of experience and scientific degree
• Fully onsite during training; potential for 1–2 days WFH afterward
• 12-month contract
• £43.82 per hour
Role Purpose:
• Ensure GMP compliance in operations
• Manage and support GMP issues through QMS processes and site governance
• Act as a GMP SME, enforcing and improving quality processes
• Support senior QA leadership in continuous improvement and regulatory compliance
Key Responsibilities:
• Review, approve, and support quality records (Deviations, CAPAs, Change Controls, Investigations, OOS)
• Escalate compliance issues and ensure timely resolution
• Identify and participate in continuous improvement initiatives
• Mentor and coach teams in cGMP practices
• Maintain audit readiness and contribute to PQS process improvements
• Provide QA SME support for manufacturing, including out-of-hours support
Required Skills & Must-Haves:
• Strong decision-making, problem-solving, and quality mindset
• Excellent communication and interpersonal skills
• Strong continuous improvement focus
• QA approval experience for Deviations, CAPAs, Change Controls, and OOSs
If you are interested please apply or send your CV to jamie.keith@cpl.com