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Microbiology Laboratory Technician

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Liverpool

On-site

GBP 25,000 - 45,000

Full time

25 days ago

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Job summary

An established industry player is seeking a Micro Analyst for a contract role in a dynamic laboratory environment. This position involves maintaining compliance with EHS and CGMP requirements, performing microbial analyses, and ensuring timely reporting of results. The ideal candidate will have experience in a GMP environment and be skilled in sample handling and laboratory systems. Join a forward-thinking company dedicated to animal health, where your contributions will support critical operations and uphold high standards of quality and safety. If you are passionate about laboratory work and eager to make an impact, this opportunity is perfect for you.

Qualifications

  • Experience in a GMP environment is essential.
  • Ability to conduct microbial analyses and maintain laboratory compliance.

Responsibilities

  • Maintain compliance with EHS and CGMP in laboratory settings.
  • Perform microbial analyses and document results accurately.

Skills

Microbial analysis
Laboratory compliance
Sample handling
Analytical data verification
Equipment calibration
Regulatory communication

Tools

Laboratory information management systems

Job description

Job Description

PE Global is currently recruiting for a Micro Analyst for a contract role with a leading multinational animal health client based in Speke.

Job Responsibilities

  1. Maintain laboratory and office areas in compliance with EHS and CGMP requirements. Archive completed laboratory documentation in a timely manner.
  2. Microbial based analyses of purchased and manufactured materials, Utilities/EM, stability samples and non-routine samples. Report and approve results using standard laboratory systems ensuring all statistical monitoring charts (paper and electronic) are updated in a timely manner.
  3. Perform all aspects of sample handling e.g sample receipt, storage and disposal as per procedures.
  4. If authorised, perform second person verification of analytical data generated in QCL as per procedures.
  5. Liaise with supervision and planners to prioritise workload to ensure OSSCE lead times and expected customer service levels are met.
  6. Conduct the equipment calibrations, maintenance and IQ/OQ that you are trained to perform. Train other QCL staff in these tasks as appropriate.
  7. Write, update and review analytical workbooks, methods and procedures.
  8. Perform analyses and document results to support method verifications, validations and transfers.
  9. Assist the QCL Scientist/Equipment group when required, by participating in analytical investigations, investigate testing and method/equipment fault finding and troubleshooting.
  10. Follow lab purchasing procedures to ensure laboratory remains sufficiently stocked with standards/reagents and consumables. If trained and authorised to do so, purchase standards/reagents and consumables.
  11. Communicate with regulatory auditors such as GQA, MHRA, FDA etc in accordance with company policy.

Requirements

  1. Previous experience within a GMP environment.

Interested candidates should submit an up to date CV.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

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