Temp - Associate QC Compliance Specialist

Regeneron Ireland; Limerick; On-site; EUR 52,000 - 70,000; Full time

Job summary

Regeneron Ireland is seeking a Temp Assoc QC Compliance Specialist to join the Quality Control team in Raheen, Limerick. The role focuses on leading investigations, deviations, and CAPAs to ensure cGMP compliance across chemistry, bioassay, microbiology, and virology laboratories.

Ideal candidates will have a BS/BA in a relevant field and 2+ years in QC or analytical sciences, with 5+ years for senior levels, demonstrating strong root cause analysis and documentation skills.

Qualifications

• BS/BA in Chemistry, Biology or related field or equivalent experience.
• 2+ years in Quality Control or Analytical Sciences in a cGMP environment.
• 5+ years for Senior Specialist in Quality Control or Analytical Sciences in a cGMP environment.

Responsibilities

• Lead and support laboratory investigations, deviations, and non-conformance activities.
• Write and review investigation reports and quality documentation.
• Perform root cause analysis and implement CAPAs.
• Support timely implementation and monitoring of corrective and preventive actions.
• Identify recurring trends and recommend process improvements to strengthen QC operations.

Skills

Laboratory investigations

Deviations handling

Root cause analysis

Quality documentation

GMP compliance

Cross-functional collaboration

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. 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.

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.

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.

Requirements:

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.

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.

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
• 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.

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.

Regeneron is a leading biotechnology company that invents life‑transforming medicines for people with serious diseases. Founded and led for over 30 years by physician‑scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA‑approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award‑winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.