Temp Assoc QC Analyst

Regeneron Pharmaceuticals; Limerick; On-site; EUR 38,000 - 52,000; Full time

Job summary

Regeneron Pharmaceuticals in Raheen, Limerick, Ireland, is seeking a TempQC Analyst to join our Sample Management team. This onsite, 12‑month contract role supports laboratory operations with a focus on quality and regulatory compliance.

You will perform chemical and biological testing on materials and products, review data for accuracy, and collaborate with internal teams to drive quality improvements. Prior GMP exposure and a Life Sciences background are preferred for this role.

Qualifications

• Experience in quality control testing and data review in a laboratory setting.
• Understanding of GMP/Regulatory expectations for analytical work.
• Attention to detail in documentation and data integrity.

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.

Skills

Laboratory testing

Quality assurance

GMP awareness

Education

BS/BA in Life Sciences

Tools

Analytical instruments

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a TempQC Analyst to join ourSample Managementteam.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

• Location : Raheen, Limerick, Ireland
• Shift: 24/7
• This is a 12-month contract position
• This is an onsite role supporting laboratory operations

What you’ll do:

• 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

The environment and physical rhythms of this role:

• 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

Let’s find out if we’re a fit:

• Requires 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

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.