Microbiology Analyst – cGMP QC & Aseptic Testing

Collins McNicholas Group

Connacht

Sur place

EUR 35 000 - 45 000

Plein temps

Il y a 2 jours
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Résumé du poste

Collins McNicholas Group is seeking a Microbiology Analyst to join the laboratory team in Westport, Co. Mayo. The role focuses on microbiological testing, environmental monitoring, and support for release and stability testing across materials and batches.

You will prepare and review lab documentation, trends results, and assist with CAPAs and deviations while ensuring compliance with cGMP and safety standards.

Qualifications

  • Third-level qualification in Microbiology or related field.
  • Minimum 12 months’ experience in a manufacturing environment, preferably pharmaceutical or aseptic processing.
  • Knowledge of microbiology, aseptic techniques and cGMP.
  • Strong attention to detail and documentation practices.

Responsabilités

  • Perform microbiological testing, including environmental monitoring, water sampling, bioburden, endotoxin, sterility, growth promotion and in-process testing.
  • Support release and stability testing of raw materials, commercial, clinical and development batches.
  • Prepare and review laboratory documentation, SOPs, protocols, investigations and reports.
  • Trend microbiological results and support investigations, deviations and CAPAs.
  • Support equipment qualification and microbiological method validation.
  • Ensure all activities comply with cGMP, quality standards and health and safety requirements.

Connaissances

Microbiology
Aseptic techniques
cGMP
Documentation practices

Formation

Third-level qualification in Microbiology

Description du poste

Collins McNicholas Group is seeking a Microbiology Analyst to join the laboratory team in Westport, Co. Mayo. The role focuses on microbiological testing, environmental monitoring, and support for release and stability testing across materials and batches.

You will prepare and review lab documentation, trends results, and assist with CAPAs and deviations while ensuring compliance with cGMP and safety standards.

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