QC Microbiology Scientist: Sterility & Validation Expert

Regeneron Pharmaceuticals; Limerick; On-site; EUR 46,000 - 75,000; Full time

Job summary

Regeneron Pharmaceuticals in Ireland seeks a QC Microbiology Associate Scientist/Scientist to join the QC Tech Resources team in Raheen, Limerick. This role contributes to a fast-growing, science-driven organization delivering medicines to patients.

You will validate sterility and bioburden methods, write technical reports, culture organisms, review procedures, and support regulatory inspections. The ideal candidate has GMP QC lab experience and strong aseptic technique, with 0–2 years for

Qualifications

• BS/BA in Microbiology or related field with 2+ years of validated experience.
• Background in pharmaceutical microbiology and GMP QC labs.
• Experience with aseptic techniques and microbial identifications.

Responsibilities

• Validate sterility, bioburden, endotoxin testing methods.
• Write technical documentation including validation reports.
• Culture organisms and characterize them for investigations.
• Review new test procedures for accuracy and compliance.
• Lead troubleshooting and investigations in microbiology.
• Support regulatory inspections and prepare assay validations.

Skills

Troubleshooting

Attention to detail

Written communication

Oral communication

Aseptic techniques

Pharmaceutical microbiology

Education

BS/BA in Microbiology or related field

Job description

Regeneron Pharmaceuticals in Ireland seeks a QC Microbiology Associate Scientist/Scientist to join the QC Tech Resources team in Raheen, Limerick. This role contributes to a fast-growing, science-driven organization delivering medicines to patients.

You will validate sterility and bioburden methods, write technical reports, culture organisms, review procedures, and support regulatory inspections. The ideal candidate has GMP QC lab experience and strong aseptic technique, with 0–2 years for