QC Microbiology Scientist

Regeneron; Limerick; On-site; EUR 46,200 - 75,400; Full time

Job summary

Regeneron in Raheen, Limerick is seeking a QC Microbiology Associate Scientist/Scientist to join the QC Tech Resources team. You will validate methods and equipment for sterility, bioburdn, and endotoxin testing while writing technical documentation.

The role requires 2+ years in pharmaceutical microbiology, GMP QC lab experience, and strong troubleshooting, attention to detail, and communication skills. The salary range is €46,200 to €75,400 per year, reflecting experience and responsibilities.

Qualifications

• BS/BA in Microbiology or related field with 2+ years of validated experience.
• Strong trouble‑shooting and problem‑solving skills.
• Excellent written and oral communication skills.
• Experience in GMP QC labs and aseptic techniques is desirable.

Responsibilities

• Validate methods and equipment for sterility, bioburden, and endotoxin testing.
• Write technical documentation including validation reports and investigations.
• Culture organisms and characterize them for investigations and cleaning development.
• Review new test procedures for accuracy and compliance.
• Evaluate new methodologies and acquire new equipment.
• Oversee contract laboratory testing to ensure quality and compliance.
• Set product specifications and alert/action levels for microbiological standards.
• Coach junior team members on GMP practices and aseptic techniques.
• Support regulatory inspections to ensure compliance.
• Demonstrate investigational skills in assay development and validation.

Skills

Troubleshooting

Attention to detail

Written and oral communication

Education

BS/BA in Microbiology or related field

Job description

Overview

At Regeneron, we use science and innovation to develop life‑changing medicines for people with serious diseases. Regeneron is currently seeking a QC Microbiology Associate Scientist / Scientist to join our QC Tech Resources team.

Location

Raheen, Limerick

Responsibilities

• Validating methods and equipment related to sterility, bioburden, endotoxin testing, and microbial identifications.
• Writing technical documentation, including position papers, validation reports, and microbiological investigations.
• Culturing organisms, conducting research, and characterizing them for use in investigations and cleaning development.
• Reviewing new test procedures and assays for accuracy and compliance.
• Evaluating and acquiring new methodologies, techniques, and equipment as needed.
• Overseeing contract laboratory testing to ensure quality and compliance.
• Setting product specifications and alert/action levels for microbiological standards.
• Leading technical troubleshooting and problem investigations.
• Reviewing assay, process, and equipment validation reports, as well as other technical documents for correctness and regulatory compliance.
• Coaching junior team members on good microbiology lab practices and modern aseptic techniques.
• Supporting and participating in regulatory inspections to ensure compliance.
• Demonstrating investigational skills and working knowledge of microbiology assay development and validation.

Environment & Physical Rhythms

• You have a proven record of working independently or as part of a team.
• Possessing a strong background in pharmaceutical microbiology, GMP working experience in QC labs, and aseptic techniques.
• You possess strong trouble‑shooting and problem‑solving skills.
• You have strong attention to detail and excellent written and oral skills.

Fit Criteria

• Assoc QC Microbiology Scientist: Minimum 0–2 years of experience.
• QC Microbiology Scientist: Minimum 2 years of experience.
• To be considered for this opportunity you should have a BS/BA or equivalent experience in Microbiology or a related field and 2+ years of validated experience, or an equivalent combination of education and experience.

Salary Range (annually)

€46,200.00 – €75,400.00

EEO Statement

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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.