QC Microbiology Analysts

S3 Science Recruitment; Greater London; On-site; GBP 30,000 - 45,000; Full time

Job summary

Join a leading biopharmaceutical company as a QC Microbiology Analyst. You will be integral to the Quality Control team, ensuring compliance with GMP standards through environmental monitoring and microbiological testing. This role suits detail-oriented individuals with a strong microbiology background who thrive in regulated environments. Collaborate with cross-functional teams and contribute to quality initiatives while maintaining high standards in a cutting-edge facility.

Qualifications

• Experience in a regulated environment like pharmaceuticals or biologics.
• Familiarity with GMP/GLP and regulatory guidelines.

Responsibilities

• Perform environmental monitoring in aseptic manufacturing areas.
• Carry out microbiological testing and interpret results.
• Support internal audits and maintain audit readiness.

Skills

Problem Solving

Communication

Education

Degree in Microbiology

Tools

Microsoft Office

Job description

Senior Recruitment Consultant - S3 Science Recruitment

An exciting opportunity has arisen for a QC Microbiology Analyst to join a cutting-edge biopharmaceutical environment focused on aseptic manufacturing. This role is ideal for individuals with a strong microbiology background and a keen eye for quality, who thrive in GMP-regulated settings.

About the Role:

You’ll be part of a collaborative Quality Control team, playing a critical role in environmental monitoring and microbiological testing of both the facility and manufactured products. Your responsibilities will include routine sampling, incubation, and analysis, ensuring all activities meet regulatory standards and internal quality expectations.

Key Responsibilities:

• Perform environmental monitoring in aseptic manufacturing areas.
• Carry out microbiological testing and interpret results.
• Ensure compliance with GMP, data integrity, and good documentation practices.
• Maintain and calibrate laboratory equipment.
• Accurately record data and report out-of-specification results with appropriate follow-up actions.
• Support internal audits, health authority inspections, and maintain audit readiness.
• Work closely with cross-functional teams including Manufacturing, QA, and Supply Chain.

What We’re Looking For:

• Degree in Microbiology or equivalent relevant experience in a regulated environment (e.g., pharmaceutical, biologics, or medical devices).
• Familiarity with GMP/GLP and regulatory guidelines (FDA, MHRA, etc.).
• Strong problem-solving skills and the ability to work both independently and as part of a team.
• Excellent communication skills, both written and verbal.
• Proficiency with Microsoft Office applications.

Key Performance Measures:

• Timely and compliant execution of environmental monitoring and QC testing.
• Effective resolution of deviations and out-of-trend results.
• Adherence to training and documentation standards.
• Contribution to continuous improvement and quality initiatives.

If you’re driven, detail-oriented, and eager to be part of a high-performing team in a regulated environment, this is your opportunity to make a meaningful impact.