Quality Control Analyst
Posted Today by i-Pharm Consulting
Negotiable
Inside
Undetermined
Runcorn, England, United Kingdom
Summary: The Quality Control Analyst I role is focused on supporting sterility assurance and contamination control in a fast-paced GMP laboratory environment. The position involves hands-on microbiological testing and environmental monitoring, with opportunities for professional growth. The analyst will be responsible for maintaining documentation and providing expertise on microbial and contamination control. This is a full-time position with a rotational shift pattern and a strong emphasis on teamwork and communication skills.
Key Responsibilities:
- Perform microbiological testing of raw materials, in-process, and finished products (e.g., sterility, endotoxin, bioburden)
- Conduct environmental monitoring in cleanrooms and filling areas
- Test utilities (Water for Injection, compressed air, room particle counts)
- Support validation, method development, and troubleshooting
- Maintain real-time GMP documentation and compile batch/quality reports
- Provide advice on microbial, hygiene, and contamination control
Key Skills:
- Degree or HNC in Microbiology/Biological Sciences + lab experience
- GMP microbiology lab experience with strong aseptic technique
- Excellent attention to detail, documentation skills, and teamwork
- Strong communication and problem-solving abilities
Salary (Rate): undetermined
City: Runcorn
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: inside IR35
Seniority Level: undetermined
Industry: Other
Job Title: Quality Control Analyst I
Location: Cheshire
Duration: 18 month contract, Inside IR35
Shift & Benefits: Rotational shift: 6am–6pm, two-week pattern (week 1: Mon, Tue, Fri–Sun; week 2: Wed–Thu) Opportunity to rotate onto 12pm–12am late shift after training 19% shift allowance
Our client, a leading pharma manufacturer, is seeking a QC Microbiology Analyst to support sterility assurance and contamination control across their products. This is a hands-on, high-impact role in a fast-paced GMP laboratory with opportunities to grow technical expertise.
What You’ll Do:
- Perform microbiological testing of raw materials, in-process, and finished products (e.g., sterility, endotoxin, bioburden)
- Conduct environmental monitoring in cleanrooms and filling areas
- Test utilities (Water for Injection, compressed air, room particle counts)
- Support validation, method development, and troubleshooting
- Maintain real-time GMP documentation and compile batch/quality reports
- Provide advice on microbial, hygiene, and contamination control
What You’ll Need:
- Degree or HNC in Microbiology/Biological Sciences + lab experience
- GMP microbiology lab experience with strong aseptic technique
- Excellent attention to detail, documentation skills, and teamwork
- Strong communication and problem-solving abilities
If you're ready to advance your QC career in a dynamic, supportive environment — apply today!
Please note: If you are interested in finding out more about this role or others, please contact Jada Kirlew at jkirlew@i-pharmconsulting.com or call: +44 (0)20 7551 0727