Temp Assoc QC Micro Analyst

Regeneron Pharmaceuticals; Limerick; On-site; EUR 35,000 - 55,000; Full time

Job summary

Regeneron Pharmaceuticals in Raheen, Limerick, Ireland is seeking an Associate QC Micro Analyst to join our Quality Control Microbiology team on a 12-month contract. The role involves performing microbiological testing and environmental monitoring to ensure product quality and patient safety.

You will review laboratory data, support investigations, and collaborate with cross-functional teams across manufacturing operations, with emphasis on accuracy, attention to detail, and compliance with

Qualifications

• BS/BA in Life Sciences or related field or equivalent.
• For Associate QC Micro Analyst: 0-2 years of relevant experience.
• For QC Micro Analyst: 2+ years of relevant experience in pharma/biotech.

Responsibilities

• Perform microbiological testing and environmental monitoring to support product quality.
• Review laboratory data, support investigations, and maintain regulatory compliance.
• Collaborate with cross-functional teams to support manufacturing operations.

Skills

Microbiology testing

Environmental monitoring

Data review & investigation

Cross-functional collaboration

Education

BS/BA in Life Sciences or related field

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking anAssociate QC Micro Analystto join ourQuality Control Microbiologyteam.

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

When & where:

• Shift Requirements:Shift pattern may be required based on business needs

• Location:Raheen, Limerick, Ireland

• This is a 12-month contract position

What you’ll do:

• Perform microbiological testing and environmental monitoring activities to support product quality and patient safety

• Review laboratory data, support investigations, and maintain compliance with quality and regulatory standards

• Collaborate with cross-functional teams to support manufacturing operations and continuous improvement initiatives

The environment and physical rhythms of this role:

• Thrive in laboratory, manufacturing, and cleanroom environments

• Demonstrate strong attention to detail and a commitment to quality

• Work effectively both independently and within cross-functional teams

• Maintain accuracy and compliance while managing competing priorities

Let’s find out if we’re a fit:

• Requires BS/BA in Life Sciences or related field or equivalent combination of education and experience

• For Associate QC Micro Analyst: 0-2 years of relevant experience

• For QC Micro Analyst: 2+ years of relevant experience, preferably in the pharmaceutical or biotechnology industry

Thrive today. Grow tomorrow.

#LI-Onsite #REGNIRLQC

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.

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.

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.

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.