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Microbiology Manager

Valtera Group LtdGalway Metropolitan Area
Hybrid · GalwayMid-Senior Level

Skills

  • MICROBIOLOGY
  • STERILE PHARMACEUTICALS
  • BIOLOGICS MANUFACTURING
  • GMP
  • ROOT CAUSE ANALYSIS
  • IMPACT ASSESSMENTS
  • EQUIPMENT QUALIFICATION
  • IQ/OQ/PQ
  • ANNEX 1 COMPLIANCE
  • ENVIRONMENTAL MONITORING
  • MEDIA FILLS
  • LABORATORY AUTOMATION

About the role

🧬 Microbiology Team Lead

📍 Galway, Ireland (some remote flex)

🕒 Permanent Position

🧠 Focus: Investigations, Projects, Equipment Qualification & Team Leadership

🧪 Sterile Pharmaceuticals / Biologics


🏢 Role Context

An exciting opportunity for a senior microbiology professional with 7+ years' experience in sterile pharmaceutical or biologics manufacturing to join a major sterile manufacturing site as Team Lead, responsible for Projects & Investigations.


You will lead microbiology investigations, support equipment and automation projects, and provide leadership to Level III microbiology personnel.


🎯 What You Will Do

  • Lead microbiology investigations from initiation through closure
  • Drive robust root cause analysis and impact assessments
  • Support and coordinate laboratory projects and automation initiatives
  • Manage equipment qualification activities including IQ/OQ/PQ documentation
  • Work with vendors, QA, Technical Services and Manufacturing stakeholders
  • Run Tier 1 operational meetings and track investigation/project progress
  • Support Annex 1 compliance activities
  • Prioritise multiple workstreams across a busy GMP laboratory
  • Mentor and support technicians within the microbiology team


✅ What We're Looking For

  • Degree in Microbiology, Pharmaceutical Sciences or related discipline
  • 7+ years' microbiology experience within pharmaceutical, biopharmaceutical or biologics manufacturing
  • Proven track record leading microbiology investigations end-to-end, not just contributing to them
  • Prior experience operating at Team Lead, Senior Microbiologist or equivalent level (even without formal direct reports)
  • Strong understanding of sterile manufacturing, environmental monitoring and Annex 1 expectations
  • Experience with media fills, equipment qualification (IQ/OQ/PQ) and GMP documentation
  • Excellent stakeholder engagement and communication skills
  • Ability to balance operational priorities with improvement initiatives


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