Supervisor Quality Control (Microbiology)

Regeneron Pharmaceuticals; Limerick; On-site; EUR 54,000 - 103,000; Full time

Job summary

Regeneron Pharmaceuticals is seeking a Supervisor, Quality Control to lead our QC team in Raheen, Limerick. This onsite leadership role supports the manufacture and release of biopharmaceutical products, driving adherence to quality systems and regulatory requirements.

The successful candidate will oversee daily QC activities, manage workload and people development, partner with cross-functional teams, and uphold a culture of continuous improvement and scientific excellence.

Qualifications

• Requires BS/BA in Life Sciences or related field; MS preferred.
• 5+ years of relevant pharmaceutical/biotech experience.
• Previous supervisory or people leadership experience required.
• Experience in GMP-regulated environment with strong communication and problem-solving skills.

Responsibilities

• Lead and supervise QC personnel, allocate workload, monitor performance.
• Ensure lab activities comply with cGMP, SOPs, and quality standards.
• Support investigations, troubleshooting, audits, and continuous improvement.
• Oversee SOPs, methods, protocols, reports, and training records.
• Manage employee development: scheduling, reviews, coaching, and training compliance.

Skills

Leadership

GMP compliance

Quality control

Problem solving

Communication

Education

BS/BA in Life Sciences

MS preferred

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Supervisor, Quality Control to join ourQuality Control (QC) team.

This position offers the opportunity to lead a team of quality control professionals supporting the manufacture and release of biopharmaceutical products for patients worldwide.

When & Where:

• Location: Raheen, Limerick, Ireland

• This is an onsite leadership role supporting Quality Control laboratory operations

• The role involves supervising daily laboratory activities and supporting cross-functional business objectives

What You’ll Do:

• Lead and supervise QC personnel, allocating workload and monitoring team performance

• Ensure laboratory activities comply with cGMP requirements, SOPs, and quality standards

• Support investigations, troubleshooting activities, audits, and continuous improvement initiatives

• Oversee documentation including SOPs, methods, protocols, reports, and training records

• Manage employee development activities including scheduling, performance reviews, coaching, and training compliance

The Environment and Physical Rhythms of This Role:

• Thrive in a fast-paced, GMP-regulated laboratory environment

• Balance leadership responsibilities with operational priorities while maintaining a strong focus on quality and safety

• Collaborate with cross-functional teams to support manufacturing and quality objectives

• Foster a culture of continuous improvement, accountability, and employee development

Let’s Find Out if We’re a Fit:

• Requires a BS/BA in Life Sciences or a related field; an MS degree is preferred

• Requires 5+ years of relevant experience within the pharmaceutical, biotechnology, or related industry

• Previous supervisory or people leadership experience is required

• Experience working in a GMP-regulated environment with strong communication and problem-solving skills

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.

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.

Salary Range (annually)

€54,200.00 - €103,200.00