QC Microbiology Analyst

BioTalent; Greater London; On-site; GBP 35,000 - 55,000; Full time

Job summary

An innovative firm is seeking a QC Microbiology Analyst to ensure product quality in a dynamic environment. This role involves performing microbiological testing, maintaining lab equipment, and authoring SOPs in compliance with industry standards. Ideal candidates will have experience in GMP-regulated settings and strong teamwork skills. Join a leading company in the pharmaceutical sector and contribute to ensuring the highest quality standards in microbiology. If you thrive in fast-paced environments and are passionate about quality assurance, this opportunity is perfect for you.

Qualifications

• 1–3 years of experience in a GMP-regulated QC Microbiology role.
• Strong understanding of aseptic techniques and microbial contamination control.

Responsibilities

• Perform routine and non-routine microbiological testing.
• Maintain and troubleshoot laboratory equipment.
• Participate in deviation investigations and root cause analysis.

Skills

Microbiological Testing

Aseptic Techniques

Environmental Monitoring

Root Cause Analysis

SOP Authoring

Job description

This range is provided by BioTalent. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

Direct message the job poster from BioTalent

Specialist Senior Quality Assurance Consultant within Pharma and Biopharma - At BioTalent

QC Microbiology Analyst – London (on site) – Competitive Package

BioTalent is seeking a highly motivated QC Microbiology Analyst to support a GCT company based in London. The successful candidate will play a critical role in ensuring that their products meet regulatory and company standards for microbiological quality throughout the manufacturing process.

Key Responsibilities:

1. Perform routine and non-routine microbiological testing including environmental monitoring, water testing, bioburden, endotoxin, and sterility testing.
2. Collect and analyze environmental and personnel monitoring samples from controlled environments.
3. Maintain and troubleshoot laboratory equipment and ensure proper calibration and maintenance.
4. Participate in deviation investigations, root cause analysis, and implementation of corrective/preventive actions.
5. Author and revise SOPs, test methods, and technical documentation in compliance with cGMP standards.

You will bring the following:

1. 1–3 years of experience in a GMP-regulated QC Microbiology related position.
2. Strong understanding of aseptic techniques, cleanroom classifications, and microbial contamination control.
3. Excellent organizational, communication, and teamwork skills.
4. Ability to work in a fast-paced, dynamic environment with changing priorities.

If this role is for you or someone you know, please reach out to me at:

Email: [e-mail]

I look forward to hearing from you!

Additional Information:

• Seniority level: Not Applicable
• Employment type: Full-time
• Job function: Quality Assurance and Science
• Industries: Pharmaceutical Manufacturing and Biotechnology Research

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