Senior Microbiology Executive – GMP & Data Integrity

Piramal Pharma Limited; United Kingdom; On-site; GBP 40,000 - 52,000; Full time

Job summary

Piramal Pharma Solutions is seeking an Executive Microbiologist with a Post-graduate degree in Microbiology and 4–6 years of microbiology experience to join our manufacturing quality labs in the UK.

You will perform environmental monitoring, microbiological testing, sterility testing, and instrumentation maintenance while adhering to cGMP/GLP and ALCOA+ data integrity standards. Audits and CAPA may be involved.

Qualifications

• Post-graduate degree in Microbiology required.
• Approximately 4–6 years of microbiology experience expected.
• Experience with environmental monitoring and microbiology testing per approved procedures.

Responsibilities

• Perform microbiological environmental monitoring in manufacturing areas and the microbiology laboratory as per approved procedures.
• Conduct microbiological testing of raw materials, packaging materials, finished products, in-process samples, stability samples, and water samples per specifications.
• Perform sterility testing of raw materials, packaging materials, and finished products.
• Maintain, calibrate, qualify, and monitor microbiology laboratory instruments and equipment.
• Ensure timely sampling and microbiological analysis of purified water, potable water, and other utility water systems.
• Maintain laboratory documentation in compliance with cGMP, GLP, ALCOA+ and data integrity requirements.
• Ensure timely data entry in laboratory software.
• Participate in audits and ensure audit readiness and regulatory compliance.

Skills

Environmental monitoring

Microbiology testing

Sterility testing

Education

Post-graduate degree in Microbiology

Job description

Piramal Pharma Solutions is seeking an Executive Microbiologist with a Post-graduate degree in Microbiology and 4–6 years of microbiology experience to join our manufacturing quality labs in the UK.

You will perform environmental monitoring, microbiological testing, sterility testing, and instrumentation maintenance while adhering to cGMP/GLP and ALCOA+ data integrity standards. Audits and CAPA may be involved.