QC Micro Analyst — Microbiology Lab (GMP)

Regeneron Pharmaceuticals

Limerick

On-site

EUR 45,000 - 65,000

Full time

9 days ago

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Job summary

Regeneron Pharmaceuticals in Raheen, Limerick, Ireland, is seeking an Associate QC Micro Analyst to join the Quality Control Microbiology team. This 12-month contract role supports microbiological testing, environmental monitoring, data review and investigations to maintain cGMP compliance.

The ideal candidate holds a BS/BA in Life Sciences or related field, with 0–2 years of experience for the Associate level, and strong teamwork and attention to quality. On-site work required.

Qualifications

  • BS/BA in Life Sciences, Microbiology, Biotechnology, or a related field.
  • 0–2 years of relevant experience for Associate level.
  • 2+ years of relevant experience, preferably in pharma/biotech for QC Micro Analyst.
  • Experience in a GMP-regulated laboratory environment is beneficial.
  • Strong communication, teamwork, and organizational skills with a focus on quality and compliance.

Responsibilities

  • Perform microbiological testing and environmental monitoring to support product quality and cGMP compliance.
  • Collect and analyse samples from manufacturing areas, cleanrooms, and utilities using approved procedures.
  • Review laboratory data and documentation; support investigations related to deviations, OOS, and OOT results.
  • Support microbiological validations, method transfers, and laboratory readiness activities.
  • Partner with Manufacturing and Quality to drive compliance and continuous improvement.

Job description

Regeneron Pharmaceuticals in Raheen, Limerick, Ireland, is seeking an Associate QC Micro Analyst to join the Quality Control Microbiology team. This 12-month contract role supports microbiological testing, environmental monitoring, data review and investigations to maintain cGMP compliance.

The ideal candidate holds a BS/BA in Life Sciences or related field, with 0–2 years of experience for the Associate level, and strong teamwork and attention to quality. On-site work required.

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