Microbiology QC Technician – cGMP Compliance & Labs

Piramal Healthcare UK Limited; Grangemouth; On-site; GBP 25,000 - 36,000; Full time

Job summary

Piramal Healthcare UK Limited is recruiting for a QC Micro Tech to join our GMP-compliant laboratory in the United Kingdom. The role focuses on performing microbiological testing of raw materials, in-process samples, finished products and environmental samples to ensure product quality and regulatory compliance.

You will operate and maintain laboratory equipment, document results, investigate out-of-specifications, support environmental monitoring and CAPA actions, and assist with method

Qualifications

• Experience in microbiology testing in regulated environments.
• Knowledge of cGMP guidelines.

Responsibilities

• Execute routine and non-routine microbiological testing, including bioburden, sterility, endotoxin, microbial ID and environmental monitoring.
• Perform media preparation, sterilization and growth promotion testing.
• Operate, maintain and calibrate laboratory equipment such as incubators, autoclaves, microscopes and spectrophotometers.
• Document testing procedures, results and observations accurately and timely, complying with documentation practices.
• Interpret test results, identify OOS results and participate in investigations.
• Participate in environmental monitoring programs including sampling and data trending.
• Assist in development and validation of new microbiological test methods.
• Contribute to investigation of deviations and CAPAs.
• Maintain a clean and organized laboratory workspace and ensure safety compliance.
• Support internal and external audits as required.
• Adhere to all company policies, procedures and cGMP guidelines.

Job description

Piramal Healthcare UK Limited is recruiting for a QC Micro Tech to join our GMP-compliant laboratory in the United Kingdom. The role focuses on performing microbiological testing of raw materials, in-process samples, finished products and environmental samples to ensure product quality and regulatory compliance.

You will operate and maintain laboratory equipment, document results, investigate out-of-specifications, support environmental monitoring and CAPA actions, and assist with method