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Senior Microbiology Team Lead

Cpl Healthcare

England

On-site

GBP 40,000 - 65,000

Full time

21 days ago

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Job summary

Cpl Healthcare is seeking a Senior Microbiology Team Lead in Oxford for a 12-month contract. This leadership role involves overseeing a team, optimizing microbiological methods, ensuring regulatory compliance, and driving improvements in product development and manufacturing processes.

Qualifications

  • 6+ years of industry experience in biotech, pharma, or industrial microbiology.
  • Demonstrated leadership experience with mentoring high-performing teams.
  • Strong knowledge of regulatory frameworks (GMP, ISO 13485, FDA, MHRA).

Responsibilities

  • Lead and manage a team of microbiologists, providing mentorship and technical direction.
  • Optimise assays for sterility, bioburden, and environmental monitoring.
  • Ensure regulatory compliance with GMP, ISO 13485, MHRA, and FDA.

Skills

Microbial identification
Molecular techniques
Biofilm research
Sterility assurance
Contamination control
Problem-solving
Communication skills

Education

PhD or MSc in Microbiology, Biotechnology, or related field

Job description

Job Title: Senior Microbiology Team Lead

Location: Oxford

Pay rate: £50 per hour

12 month contract

Cpl Life Sciences is working exclusively with a biotech company seeking a Senior Microbiology Team Lead to oversee and drive microbiological research, method development, and regulatory compliance. This leadership role involves managing a team of microbiologists, optimising assays, and ensuring microbiological integrity across product development and manufacturing processes.

Key Responsibilities:

·Lead and manage a team of microbiologists, providing mentorship and technical direction.

·Optimise and oversee microbiological assays for sterility, bioburden, endotoxin, environmental monitoring, and antimicrobial susceptibility testing.

·Develop, validate, and implement new microbiological methods to support product innovation.

·Ensure regulatory compliance with GMP, ISO 13485, MHRA, and FDA requirements, supporting audits and inspections.

·Troubleshoot microbiological issues in manufacturing, product development, and quality control.

·Drive continuous improvement initiatives for microbiological testing, working cross-functionally with R&D, Quality, and Manufacturing teams.

·Stay updated with industry advancements, regulatory changes, and emerging microbiological technologies, implementing best practices to enhance efficiency and compliance.

Essential Skills & Experience:

·PhD or MSc in Microbiology, Biotechnology, or a related field, with 6+ years of industry experience (biotech, pharma, or industrial microbiology).

·Strong expertise in microbial identification, molecular techniques (PCR, NGS), biofilm research, sterility assurance, and contamination control.

·Experience in method development, validation, and troubleshooting of microbiological assays.

·Demonstrated leadership experience, with a proven track record of mentoring and developing high-performing teams.

·Strong knowledge of regulatory frameworks (GMP, ISO 13485, FDA, MHRA) and experience supporting audits.

·Excellent problem-solving skills, with the ability to work both independently and collaboratively.

·Strong written and verbal communication skills, with experience presenting findings and influencing stakeholders.

If you are interested, please apply now or send your CV to daniel.bailey@cpl.com

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