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Microbiologist Analyst

PE Global (UK)

Liverpool

On-site

GBP 60,000 - 80,000

2 days ago
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Job summary

Ein führendes multinationales Unternehmen im Bereich Tiergesundheit sucht einen Micro Analysten für eine spannende Vertragsrolle. In dieser Position sind Sie verantwortlich für die Durchführung mikrobiologischer Analysen, die Wartung von Laborbereichen und die Einhaltung von GMP-Vorgaben. Sie arbeiten eng mit verschiedenen Teams zusammen, um sicherzustellen, dass alle Laborarbeiten effizient und gemäß den höchsten Standards durchgeführt werden. Diese Rolle bietet die Möglichkeit, in einem dynamischen Umfeld zu arbeiten und zur Qualitätssicherung in der Tiergesundheitsbranche beizutragen.

Qualifications

  • Erfahrung in einem GMP-Umfeld ist erforderlich.
  • Fähigkeit zur Durchführung mikrobiologischer Analysen.

Responsibilities

  • Wartung der Labor- und Bürobereiche gemäß EHS- und CGMP-Anforderungen.
  • Durchführung mikrobiologischer Analysen und Dokumentation der Ergebnisse.

Skills

GMP Compliance

Microbial Analysis

Statistical Monitoring

Sample Handling

Analytical Investigations

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.

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