Job Description

QC Microbiology Analyst 

Location: Ireland, Dublin (Onsite) Shift: 12/7 pattern possible

Duration: 12 Months

Bring your microbiology expertise to a GMP-regulated lab and help ensure every product meets the highest quality and safety standards.

Key Responsibilities

• Perform bioburden and endotoxin testing of drug product, drug substance, raw materials, and water utilities
  
  
• Conduct microbial identification using MALDI / MicroSeq and support PCR testing
  
  
• Carry out environmental monitoring in cleanrooms (Grades A–D, predominantly Grade C)
  
  
• Perform utility sampling of water systems, clean steam, compressed air, and gas
  
  
• Support isolator batch monitoring and handle biological indicators (issuance, receipt, testing)
  
  
• Participate in Aseptic Process Simulations (APS/media fills) and reconciliation of media-filled units
  
  
• Investigate and document OOS/OOT events and deviations, maintaining accurate GMP documentation
  
  
• Review and reconcile laboratory paperwork and reports
  
  
• Support cross-functional teams to meet production and qualification schedules
  
  
• Ensure adherence to GMP, safety, and lean laboratory practices, maintaining high standards of housekeeping
  
  
• Assist in authoring and reviewing SOPs, training documents, and laboratory procedures
  
  

Requirements

• Bachelor’s or Level 8 degree in Microbiology or related Life Sciences
  
  
• 1-2 years’ experience in a pharmaceutical/healthcare laboratory or GMP microbiology role
  
  
• Hands-on experience in aseptic technique, environmental monitoring, utility sampling, or product testing
  
  
• Cleanroom experience is essential
  
  
• Excellent written and verbal communication skills and strong attention to detail
  
  
• Ability to work collaboratively in a team-based environment
  
  
• Willingness to work a 12/7 shift pattern if required
  
  

Must Have

• Utility sampling of compressed air and gas.

• Isolator batch-related monitoring.

• Issuance, receipt, and testing of biological indicators.

• Reconciliation and inspection of media fill units, and participation in media fills (APS).

Desirable

• Sterility testing experience
  
  
• Experience with isolator monitoring and biological indicators
  
  
• Compressed air/gas sampling experience
  
  
• MALDI / MicroSeq microbial identification or PCR experience
  
  
• Familiarity with laboratory systems such as MODA, Empower, CIMS, LIMS, LES, or Veeva Vault
  
  
• Exposure to investigations, lean lab practices, or 6S methodologies
  
  

If you are passionate about microbiology, quality control, and GMP-compliant laboratory work, and want to make an impact in a dynamic pharmaceutical environment – APPLY TODAY!