This range is provided by Cpl Life Sciences. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
Principal Consultant – Quality/Scientific
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.
Experience Required:
• 5–10 years of experience and scientific degree
• Fully onsite during training; potential for 1–2 days WFH afterward
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:
1. Review, approve, and support quality records (Deviations, CAPAs, Change Controls, Investigations, OOS)
2. Escalate compliance issues and ensure timely resolution
3. Identify and participate in continuous improvement initiatives
4. Mentor and coach teams in cGMP practices
5. Maintain audit readiness and contribute to PQS process improvements
6. Provide QA SME support for manufacturing, including out-of-hours support
Required Skills & Must-Haves:
1. Strong decision-making, problem-solving, and quality mindset
2. Excellent communication and interpersonal skills
3. 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.
Seniority level
Mid-Senior level
Employment type
Contract
Job function
Quality Assurance
Industries
Pharmaceutical Manufacturing
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