Job Description

• HEPA filter testing, airflow visualization, non-viable particulate monitoring.
• Validation of cleanroom environments, LAFs, BSCs, fume cupboards and containment suites.
• Temperature, humidity and pressure control verification.
• Commissioning & test balancing (TAB), system optimization, troubleshooting.
• Audit support and GMP documentation.

• CTCB-I Professional Certification (mandatory).
• 3+ years in cleanroom validation within pharma/biotech/medical devices.
• Strong knowledge of cGMP, ISO standards and validation protocols.
• Compliance with Health & Safety legislation.
  
  

For further information on this role please contact Regina Carroll on +353 86 0100 903 or email jobs@hero.ie
Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/.

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