Temp Assoc QC Micro Analyst

Regeneron Pharmaceuticals; Limerick; On-site; EUR 45,000 - 65,000; Full time

Job summary

Regeneron Pharmaceuticals in Raheen, Limerick, Ireland, is seeking an Associate QC Micro Analyst to join the Quality Control Microbiology team. This 12-month contract role supports microbiological testing, environmental monitoring, data review and investigations to maintain cGMP compliance.

The ideal candidate holds a BS/BA in Life Sciences or related field, with 0–2 years of experience for the Associate level, and strong teamwork and attention to quality. On-site work required.

Qualifications

• BS/BA in Life Sciences, Microbiology, Biotechnology, or a related field.
• 0–2 years of relevant experience for Associate level.
• 2+ years of relevant experience, preferably in pharma/biotech for QC Micro Analyst.
• Experience in a GMP-regulated laboratory environment is beneficial.
• Strong communication, teamwork, and organizational skills with a focus on quality and compliance.

Responsibilities

• Perform microbiological testing and environmental monitoring to support product quality and cGMP compliance.
• Collect and analyse samples from manufacturing areas, cleanrooms, and utilities using approved procedures.
• Review laboratory data and documentation; support investigations related to deviations, OOS, and OOT results.
• Support microbiological validations, method transfers, and laboratory readiness activities.
• Partner with Manufacturing and Quality to drive compliance and continuous improvement.

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking an Associate QC Micro Analyst to join our Quality Control Microbiology team. 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, patient safety, and cGMP compliance.
• Collect and analyse samples from manufacturing areas, cleanrooms, and utilities using approved laboratory procedures.
• Review laboratory data, complete documentation, and support investigations related to deviations, OOS, and OOT results.
• Support microbiological validations, method transfers, and laboratory readiness activities.
• Partner with Manufacturing, Quality, and other cross-functional teams to drive compliance and continuous improvement.

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.
• Apply critical thinking and problem-solving skills to support investigations and process improvements.

Let’s find out if we’re a fit:

• Requires a BS/BA in Life Sciences, Microbiology, Biotechnology, or a related field, or an 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.
• Experience in a GMP-regulated laboratory environment is beneficial.
• Strong communication, teamwork, and organizational skills with a focus on quality and compliance.

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:

• 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.

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. For more information about on-site expectations for your role and location, please speak with your recruiter and hiring manager.

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.