Temp - Associate QC Compliance Specialist

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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 Temp Assoc QC Compliance Specialist to join our Quality Control team. This position offers the opportunity to support quality, compliance, and continuous improvement activities across our QC laboratories, ensuring investigations and quality processes are completed to the highest standards in a GMP-regulated environment. When & Where: • Location: Raheen, Limerick, Ireland. • This role supports QC laboratories including Chemistry, Bioassay, Microbiology, and Virology. • You will collaborate with cross-functional teams to drive compliance and quality excellence. What you'll do: • Lead and support laboratory investigations, deviations, and non-conformance activities. • Write and review investigation reports and associated quality documentation. • Perform root cause analysis and partner with teams to identify effective CAPAs. • Support the timely implementation and monitoring of corrective and preventative actions. • Identify recurring trends and recommend process improvements to strengthen Quality Control operations. The environment and physical rhythms of this role: • Thrive in a fast-paced GMP-regulated environment with a strong focus on quality and compliance. • Balance multiple priorities while meeting deadlines and maintaining attention to detail. • Collaborate effectively with laboratory, quality, and cross-functional teams. • Use critical thinking and problem-solving skills to resolve complex quality issues. • Drive a culture of continuous improvement and operational excellence. Let's find out if we're a fit: • Requires a BS/BA in Chemistry, Biology, or a related scientific field, or an equivalent combination of education and experience. • Associate Specialist: Relevant degree and/or industry experience. • Specialist: 2+ years of Quality Control or Analytical Sciences experience, including laboratory investigation experience in a cGMP environment. • Senior Specialist: 5+ years of Quality Control or Analytical Sciences experience, including laboratory investigation experience in a cGMP environment. • Experience with investigations, deviations, CAPAs, and root cause analysis is highly desirable.     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, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, p

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