PERMANENT, FULL-TIME

Are you a detail-oriented and proactive Quality professional seeking your next opportunity in a dynamic and regulated environment? If so, GMP Manufacturing Limited has an exciting opportunity for you!

JOB SUMMARY:

Reporting to the Microbiological Manager, you will play a crucial role in ensuring the microbiological quality and compliance of our products through rigorous testing, analysis, and reporting. You will collaborate closely with cross-functional teams to sustain and enhance our quality benchmarks.

ESSENTIAL SKILLS:

Ø Experience in a Pharmaceutical or Healthcare environment is essential.
Ø A degree-level qualification in Microbiology or a related field and/or 2 years’ experience in a similar role.
Ø Comprehensive and understanding of complex manufacturing processes.
Ø Knowledge of Good Manufacturing Practice type systems and practices in a manufacturing environment.
Ø Ability to communicate and express ideas clearly, across all levels of the organisation
Ø Skilled in Microsoft Office applications.
What We Offer:
Ø Company Benefit Scheme
Ø Pension Scheme
Ø Employee Assistance Program – supporting your well-being
Ø Onsite Parking
Ø Bereavement Leave
Ø Birthday Leave
Ø Volunteering Paid Off
Join GMP Manufacturing Limited and play an integral part in driving microbiological quality excellence across our operations!
Job Types: Full-time, Permanent
Pay: From £25,500.00 per year

Benefits:

• Bereavement leave
• Company pension
• Employee discount
• Health & wellbeing programme
• Store discount

Schedule:

• Monday to Friday

Work Location: In person
Application deadline: 25/07/2025
Reference ID: GMPM/QC/25/00

Ø Perform microbiological testing and sampling on raw materials, intermediates, and finished products, adhering to Good Practices and specific methods.
Ø Generate and execute environmental monitoring procedures, protocols and activities.
Ø Act as an SME for microbiology-related investigations to ensure timely resolution.
Ø Support the timely release of products to clients by operating within agreed lead times.
Ø Ensure all job-related activities comply fully with relevant Health and Safety legislation to uphold a safe and secure working environment.
Ø Ensure completion of all documentation in accordance with ALCOA principles (Attributable, Legible, Contemporaneous, Original and Accurate).
Ø Ensure all Microbiological testing activities align with Good Manufacturing Practices (GMP) expectations.
Ø Actively engage in the timely progression of Out of Specification (OOS) investigations.
Ø Maintain appropriate levels of housekeeping in all Quality Control (QC- Microbiology) areas to foster a clean and organised work environment.
Ø Contribute to the creation and completion of all Quality Management System-related documents such as Standard Operating Procedures (SOPs), Deviations and Change Controls.
Ø Coordinate with 3rd party laboratories to ensure prompt sending of samples and reporting of results received.
Ø Any other duties reasonably required.
Ø Maintain a positive, proactive, and can-do attitude