QC Micro Analyst

Limerick, IEFull-time2026-10-08 → 2026-11-10

Core

Perform microbiological testing and environmental monitoring to ensure the quality and safety of medicines in cGMP manufacturing operations.

Role type

Associate QC Micro Analyst

Builds

Production pharmaceutical products

Domain

Pharmaceutical manufacturing / Microbiology

Required skills

Microbiological laboratory techniques, Environmental monitoring, GMP compliance, Data integrity, Documentation practices, Microbial identification

Preferred skills

Experience in GMP/pharmaceutical/biotechnology environments, Bioburden testing, Endotoxin testing

Technologies

None stated

Responsibilities

Perform microbiological testing to support cGMP manufacturing operations, Conduct environmental monitoring activities (viable/non-viable air, surface, settling plates), Collect and analyze samples for bioburden, endotoxin, and microbial identification, Review laboratory data and complete documentation, Ensure compliance with GMP requirements and SOPs, Collaborate with cross-functional teams to support manufacturing operations

Seniority

Associate, 0-2 years experience

About Regeneron

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regu