QC Analyst — Life Sciences & GMP in 24/7 Lab

Regeneron Pharmaceuticals, Inc; Limerick; Sur place; EUR 22 000 - 34 000; Plein temps

Résumé du poste

Regeneron Pharmaceuticals, Inc. is seeking a QC Analyst to join our Quality Control Laboratory team in Raheen, Limerick, Ireland. You will perform chemical and/or biological testing on raw materials, in-process materials, finished products, and stability samples, with a focus on accuracy and regulatory compliance.

You will document testing data, review results, and support instrument calibration, SOPs, and method validation while working in a regulated lab environment and 24/7 shift operation.

Qualifications

• Bachelor's degree in Life Sciences or related scientific discipline.
• Experience in a laboratory, quality control, or regulated environment preferred.
• Strong attention to detail with accurate data documentation.

Responsabilités

• Perform chemical and/or biological testing on raw materials, in-process materials, finished products, stability samples, and research samples.
• Gather, analyze, and document testing data to support quality and compliance requirements.
• Review laboratory results and identify, investigate, and elevate quality anomalies when appropriate.
• Calibrate and verify laboratory instruments and equipment to ensure reliable and accurate testing.
• Write, revise, and follow SOPs, test methods, and laboratory documentation.
• Support analytical method validation, method transfer activities, and continuous improvement initiatives.
• Maintain laboratory supplies and ensure a safe, organized, and inspection-ready workspace.
• Collaborate with cross-functional teams to support product quality and regulatory compliance.

Connaissances

GMP knowledge

Documentation skills

Regulated environment

Attention to detail

Formation

Bachelor's degree in Life Sciences or related

Description du poste

Regeneron Pharmaceuticals, Inc. is seeking a QC Analyst to join our Quality Control Laboratory team in Raheen, Limerick, Ireland. You will perform chemical and/or biological testing on raw materials, in-process materials, finished products, and stability samples, with a focus on accuracy and regulatory compliance.

You will document testing data, review results, and support instrument calibration, SOPs, and method validation while working in a regulated lab environment and 24/7 shift operation.