QC Analyst, GMP Lab (24/7) – Impact in Life Sciences

Regeneron Pharmaceuticals, Inc.; Limerick; Presencial; EUR 23 000 - 35 000; Tempo integral

Resumo da oferta

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick, Ireland, invites applications for a QC Analyst to join the Quality Control Laboratory.

This on-site role supports chemical and biological testing, data documentation, and adherence to GMP in a regulated lab environment. You will perform testing on materials and finished products, calibrate instruments, write and revise SOPs, and collaborate with cross-functional teams to ensure product quality and regulatory compliance.

Qualificações

• Bachelor's degree in Life Sciences or related discipline.
• Experience in a laboratory, quality control, or regulated environment preferred.
• Strong attention to detail with accurate data documentation.
• Knowledge of GMP and regulatory requirements is advantageous.
• Effective communication and collaboration skills.

Responsabilidades

• 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.

Conhecimentos

Attention to detail

Communication skills

Collaboration

Formação académica

Bachelor's degree in Life Sciences

Descrição da oferta de emprego

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick, Ireland, invites applications for a QC Analyst to join the Quality Control Laboratory.

This on-site role supports chemical and biological testing, data documentation, and adherence to GMP in a regulated lab environment. You will perform testing on materials and finished products, calibrate instruments, write and revise SOPs, and collaborate with cross-functional teams to ensure product quality and regulatory compliance.