QC Microbiologist – Pharma Microbiology & Sterility

PE Global; Westport; On-site; EUR 42,000 - 60,000; Full time

Job summary

PE Global is currently recruiting a QC Microbiologist for a leading pharmaceutical client based in Westport, Ireland. This contract role involves performing routine microbiology testing, environmental monitoring of cleanrooms, and batch testing across raw materials, utilities and development batches as part of the Global Stability program.

You will work to cGMP standards, support release and stability testing, ensure timely reporting and documentation, and contribute to investigations and CAPAs

Qualifications

• 3rd Level Qualification in Microbiology or equivalent.
• At least 12 months in a manufacturing environment, preferably aseptic processing.
• Working knowledge of Pharmaceutical Industry and sterile processing.
• Strong background in Aseptics and/or Microbiology.
• Ensures testing completed within agreed turnaround times.
• Compliance with product licenses, cGMP and health & safety standards.

Responsibilities

• Environmental Monitoring
• water sampling
• bioburden
• in-process testing
• endotoxin
• growth promotion
• Sterility testing
• APET
• Antibiotic Assay
• Report writing
• Draft and review SOPs, protocols, training modules, investigations, reports, CAPAs and deviations
• Trending of results and investigations into adverse or out-of-limit results
• Validation of equipment and microbiology test methods

Skills

Microbiology

Aseptic processing

Environmental Monitoring

Regulatory compliance

cGMP

Education

3rd Level Qualification in Microbiology or equivalent

Job description

PE Global is currently recruiting a QC Microbiologist for a leading pharmaceutical client based in Westport, Ireland. This contract role involves performing routine microbiology testing, environmental monitoring of cleanrooms, and batch testing across raw materials, utilities and development batches as part of the Global Stability program.

You will work to cGMP standards, support release and stability testing, ensure timely reporting and documentation, and contribute to investigations and CAPAs