Senior Microbiologist: EtO Sterilization & GMP Lead

Baker Finn Recruitment

South Dublin

On-site

EUR 70,000 - 90,000

Full time

3 days ago
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Job summary

Baker Finn Recruitment has partnered with a South Dublin manufacturing site to hire a Senior Microbiologist for a 12-month fixed-term contract. The role is fully onsite and focuses on microbiology leadership, EtO sterilization, GLP, and cleanroom compliance to ensure patient safety and regulatory adherence.

The successful candidate will act as site SME, collaborate with Quality and Manufacturing teams, drive investigations, CAPA, data integrity, and maintain inspection readiness across ISO and

Qualifications

  • Degree in Microbiology or a related science.
  • 5+ years' experience in medical device, pharma, or biotech.
  • Strong expertise in GLP, cleanrooms, validation and sterilization.
  • EtO sterilization experience advantageous.
  • Proven ability to work cross-functionally in regulated environments.

Responsibilities

  • SME oversight for EtO sterilization, GLP labs, and environmental monitoring.
  • Review/approve sterilization cycles, microbiological data, and product release.
  • Set microbiological and sterilization quality standards and ensure consistency.
  • Ensure ISO 11135, ISO 10993, ISO 13485, FDA QSR/QMSR compliance.
  • Lead investigations, CAPA, and non-conformance resolution.
  • Maintain laboratory safety, equipment readiness, and data integrity.
  • Maintain audit and inspection readiness.

Skills

GLP expertise
Environmental monitoring
CAPA investigations
Cross-functional collaboration
Quality mindset

Education

Degree in Microbiology or related Science

Job description

Baker Finn Recruitment has partnered with a South Dublin manufacturing site to hire a Senior Microbiologist for a 12-month fixed-term contract. The role is fully onsite and focuses on microbiology leadership, EtO sterilization, GLP, and cleanroom compliance to ensure patient safety and regulatory adherence.

The successful candidate will act as site SME, collaborate with Quality and Manufacturing teams, drive investigations, CAPA, data integrity, and maintain inspection readiness across ISO and

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