QC Micro Analyst: Impactful Microbiology in GMP Lab

Regeneron Pharmaceuticals, Inc.; Limerick; On-site; EUR 22,000 - 34,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Limerick is seeking an Associate QC Micro Analyst to join the Quality Control Microbiology team in Raheen. The role involves performing microbiological testing to support cGMP manufacturing and product quality.

You will conduct environmental monitoring, log and analyze samples for bioburdn and endotoxin testing, review data, and ensure compliance with GMP standards. Requires a BS/BA in Microbiology or Life Sciences and 0-2 years' experience; on-site with

Qualifications

• Bachelor’s degree in Microbiology, Biotechnology, Life Sciences or related field (or equivalent).
• 0–2 years of relevant laboratory experience for Associate level.
• Experience in GMP/pharmaceutical/regulated environment is advantageous.
• Strong understanding of microbiological lab techniques and good documentation practices.

Responsibilities

• Perform microbiological testing to support cGMP manufacturing operations and product quality.
• Conduct environmental monitoring: air, surface and settling plate sampling.
• Collect, log and analyze samples for bioburden, endotoxin and microbial identification testing.
• Review laboratory data, document conclusions and support investigations.
• Ensure compliance with GMP requirements, SOPs and regulatory standards.

Skills

Microbiology

Documentation

Education

BS/BA in Microbiology or Life Sciences

Job description

Regeneron Pharmaceuticals, Inc. in Limerick is seeking an Associate QC Micro Analyst to join the Quality Control Microbiology team in Raheen. The role involves performing microbiological testing to support cGMP manufacturing and product quality.

You will conduct environmental monitoring, log and analyze samples for bioburdn and endotoxin testing, review data, and ensure compliance with GMP standards. Requires a BS/BA in Microbiology or Life Sciences and 0-2 years' experience; on-site with