GMP QC Analyst, Drug Product Testing

Regeneron Pharmaceuticals, Inc; Munster; On-site; EUR 25,000 - 40,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Ireland (Raheen, Limerick) is seeking a QC Analyst (Drug Product) to join our QC Chemistry, Drug Product Testing team. This role tests according to approved procedures to support release and stability programs and reviews data to ensure GMP compliance.

You'll help validate and transfer analytical methods, investigate lab events, write SOPs, maintain training compliance, and manage supplies while driving continuous improvement.

Qualifications

• Requires a BS/BA in Life Sciences or related field.
• Minimum of 2 years of relevant industry experience as a QC Analyst.
• Experience reviewing analytical testing in a GMP‑regulated lab is preferred.
• Strong organizational, communication, and teamwork skills with a commitment to quality.

Responsibilities

• Perform testing according to approved procedures to support product release and stability.
• Review laboratory testing documentation and data for GMP compliance and quality standards.
• Support validation, qualification, and transfer of analytical methods and procedures.
• Investigate lab events and collaborate with cross‑functional teams to resolve issues.
• Write, revise, and maintain controlled test procedures and SOPs.
• Participate in training activities and maintain training compliance.
• Manage laboratory supplies and materials for routine operations.
• Support continuous improvement initiatives to enhance lab performance.

Skills

GMP knowledge

Documentation review

Analytical testing

Problem solving

Attention to detail

Written & oral communication

Education

BS/BA in Life Sciences or related field

Job description

Regeneron Pharmaceuticals, Inc. in Ireland (Raheen, Limerick) is seeking a QC Analyst (Drug Product) to join our QC Chemistry, Drug Product Testing team. This role tests according to approved procedures to support release and stability programs and reviews data to ensure GMP compliance.

You'll help validate and transfer analytical methods, investigate lab events, write SOPs, maintain training compliance, and manage supplies while driving continuous improvement.