Temp Assoc QC Analyst

About the role

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Temp QC Analyst to join our Sample Management team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Responsibilities

• Perform chemical and biological testing on raw materials, in-process materials, finished products, and stability samples
• Review and document analytical data, ensuring compliance with quality standards and regulatory requirements
• Support method validation, technology transfer activities, and continuous improvement initiatives
• Maintain laboratory equipment, supplies, and documentation in accordance with GMP requirements
• Collaborate with internal teams and external partners to support quality and operational excellence

Work environment

• Thrive working in a laboratory environment with a strong focus on quality and compliance
• Demonstrate strong attention to detail and accuracy when performing testing and reviewing data
• Balance multiple priorities while meeting timelines and maintaining regulatory standards
• Work effectively both independently and as part of cross-functional teams
• Participate in ongoing training and development activities

Requirements

• BS/BA in Life Sciences or related field, or an equivalent combination of education and experience
• For Associate QC Analyst: 0-2 years of relevant experience
• For QC Analyst: 2+ years of relevant experience, preferably in a GMP-regulated pharmaceutical or biotechnology environment
• Strong attention to detail and ability to work effectively in a team-based laboratory environment

Schedule

This is a 12-month contract position with a 24/7 shift pattern, onsite in Raheen, Limerick, Ireland.