QC Analyst

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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 QC Sample Management Specialist to join our Quality Control team. This role offers the opportunity to play a critical part in supporting QC operations by managing samples, maintaining compliance, and ensuring accurate tracking and documentation throughout the testing lifecycle. When & Where: • Location: Raheen, Limerick, Ireland. • This is a full-time onsite position. • This role supports Quality Control laboratory operations and cross-functional teams across the site. What You'll Do: • Receive, verify, track, and manage QC samples throughout their lifecycle using Laboratory Information Management Systems (LIMS). • Maintain chain of custody and ensure samples are handled in accordance with approved procedures and GMP requirements. • Support sample shipment activities, inventory management, storage, and disposal processes. • Review and document test results, reporting any quality concerns or anomalies. • Maintain laboratory supplies and support laboratory readiness activities. • Assist with controlled temperature unit monitoring and preventive maintenance activities. • Verify instrument and equipment calibration prior to use. • Write, update, and maintain work instructions and standard operating procedures (SOPs). • Collaborate with internal stakeholders and external partners to support operational excellence and compliance. • Support continuous improvement initiatives, method validations, and project activities as required. The Environment and Physical Rhythms of This Role: • Thrive in a fast-paced laboratory environment with a strong focus on quality, compliance, and accuracy. • Balance multiple priorities while maintaining attention to detail. • Work effectively both independently and as part of cross-functional teams. • Take ownership of tasks, projects, and process improvement opportunities. • Communicate effectively with colleagues across a variety of functions and departments. • Participate in ongoing training and development activities. Let's Find Out if We're a Fit: • Requires a BS/BA in Life Sciences or a related field, or an equivalent combination of education and experience. • Experience in a laboratory, pharmaceutical, biotechnology, or GMP-regulated environment is preferred. • Strong attention to detail and organizational skills. • Ability to manage multiple priorities while maintaining accuracy and compliance. • Strong communication and collaboration skills with the ability to work effectively in a team-based environment.   Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.   Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, spec

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