QC Microbiology Scientist – Validation & Microbial Analysis

Regeneron Pharmaceuticals, Inc; Munster; On-site; EUR 37,000 - 75,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick, Ireland is seeking a QC Microbiology Associate Scientist to join the QC Tech Resources team. The role involves validating sterility-related methods, writing technical reports, culturing organisms, and reviewing procedures for compliance.

You will lead troubleshooting, oversee external labs, and coach junior staff while maintaining GMP standards in an on-site setting. BS/BA in Microbiology with 2+ years of experience preferred.

Qualifications

• BS/BA in Microbiology or related field with 2+ years of validated experience.
• Minimum 0-2 years for Assoc QC Microbiology Scientist; 2+ years for QC Microbiology Scientist.
• Experience in GMP QC labs and aseptic techniques is desirable.

Responsibilities

• Validate methods and equipment related to sterility, bioburden, endotoxin testing, and microbial identifications.
• Write technical documentation including validation reports and investigations.
• Culture organisms and characterize them for investigations and cleaning development.
• Review new test procedures and assays for accuracy and compliance.
• Evaluate and acquire new methodologies, techniques, and equipment.
• Oversee contract laboratory testing to ensure quality and compliance.
• Set product specifications and alert/action levels for microbiological standards.
• Lead technical troubleshooting and problem investigations.
• Review validation reports and regulatory documents for correctness.
• Coach junior team members on good microbiology lab practices and aseptic techniques.

Skills

Pharmaceutical microbiology

GMP QC labs

Aseptic techniques

Troubleshooting

Education

BS/BA in Microbiology or related field

2+ years validated experience

Job description

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick, Ireland is seeking a QC Microbiology Associate Scientist to join the QC Tech Resources team. The role involves validating sterility-related methods, writing technical reports, culturing organisms, and reviewing procedures for compliance.

You will lead troubleshooting, oversee external labs, and coach junior staff while maintaining GMP standards in an on-site setting. BS/BA in Microbiology with 2+ years of experience preferred.