Temp - Associate QC Compliance Specialist

Regeneron Pharmaceuticals, Inc.; Limerick; On-site; EUR 55,000 - 75,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Temp Assoc QC Compliance Specialist to join the Quality Control team in Limerick, Ireland. You will lead investigations across Chemistry, Bioassay, Microbiology and Virology labs, writing reports and driving quality improvements.

The role requires experience in QC or analytical sciences, with strong problem-solving skills and a focus on compliant, timely CAPA implementation in a GMP environment.

Qualifications

• BS/BA in Chemistry, Biology, or a related scientific field or equivalent experience.
• Experience in QC/Analytical Sciences and laboratory investigations in a cGMP environment.
• Strong documentation and reporting skills for investigations and CAPAs.

Responsibilities

• Lead and support laboratory investigations, deviations and non-conformances.
• Write and review investigation reports and quality documentation.
• Perform root cause analysis and partner with teams to identify effective CAPAs.
• Support timely implementation and monitoring of corrective and preventative actions.
• Identify recurring trends and propose process improvements in QC operations.

Skills

Quality Control

Laboratory investigations

CAPA

Root cause analysis

Analytical Sciences

Education

BS/BA in Chemistry or Biology

Job description

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.

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? 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, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about on-site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.