QC Analyst

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

Job summary

Regeneron Pharmaceuticals, Inc. in Raheen, Limerick, Ireland, is seeking a QC Sample Management Specialist to join our Quality Control team. This onsite, full-time role focuses on managing QC samples, maintaining chain of custody, and ensuring GMP-compliant documentation throughout the testing lifecycle.

You will work with LIMS to track samples, support shipment, inventory, and storage, verify calibrations, and contribute to SOPs and continuous improvement within a cross-functional environment.

Qualifications

• Requires a BS/BA in Life Sciences or related field (or equivalent).
• Experience in a laboratory, pharmaceutical, biotechnology, or GMP-regulated environment is preferred.
• Strong attention to detail and organizational skills.
• Ability to manage multiple priorities while maintaining accuracy and compliance.
• Strong communication and collaboration skills in a team-based environment.

Responsibilities

• Receive, verify, track, and manage QC samples using LIMS.
• Maintain chain of custody and GMP compliance.
• Support sample shipment, inventory, storage, and disposal processes.
• Review and document test results, reporting any quality concerns or anomalies.
• Maintain laboratory supplies and support laboratory readiness activities.
• Assist with controlled temperature monitoring and preventive maintenance activities.
• Verify instrument calibration prior to use.
• Write, update, and maintain SOPs and work instructions.
• Collaborate with internal stakeholders and external partners to support compliance.
• Support continuous improvement initiatives, method validations, and project activities as required.

Skills

Attention to detail

Communication skills

Teamwork

Education

BS/BA in Life Sciences

Tools

LIMS

GMP knowledge

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases.

Regeneron is currently seeking a QC Sample Management Specialist to join our Quality Control team. This role offers the opportunity to play a critical part in supporting QC operations by managing samples, maintaining compliance, and ensuring accurate tracking and documentation throughout the testing lifecycle.

When & Where:

Location: Raheen, Limerick, Ireland. Shift: 24/7 This is a full-time onsite position. This role supports Quality Control laboratory operations and cross-functional teams across the site.

What You'll Do:

• Receive, verify, track, and manage QC samples throughout their lifecycle using Laboratory Information Management Systems (LIMS).
• Maintain chain of custody and ensure samples are handled in accordance with approved procedures and GMP requirements.
• Support sample shipment activities, inventory management, storage, and disposal processes.
• Review and document test results, reporting any quality concerns or anomalies.
• Maintain laboratory supplies and support laboratory readiness activities.
• Assist with controlled temperature unit monitoring and preventive maintenance activities.
• Verify instrument and equipment calibration prior to use.
• Write, update, and maintain work instructions and standard operating procedures (SOPs).
• Collaborate with internal stakeholders and external partners to support operational excellence and compliance.
• Support continuous improvement initiatives, method validations, and project activities as required.

The Environment and Physical Rhythms of This Role:

• Thrive in a fast-paced laboratory environment with a strong focus on quality, compliance, and accuracy.
• Balance multiple priorities while maintaining attention to detail.
• Work effectively both independently and as part of cross-functional teams.
• Take ownership of tasks, projects, and process improvement opportunities.
• Communicate effectively with colleagues across a variety of functions and departments.
• Participate in ongoing training and development activities.

Let's Find Out if We're a Fit:

• Requires a BS/BA in Life Sciences or a related field, or an equivalent combination of education and experience.
• Experience in a laboratory, pharmaceutical, biotechnology, or GMP-regulated environment is preferred.
• Strong attention to detail and organizational skills.
• Ability to manage multiple priorities while maintaining accuracy and compliance.
• Strong communication and collaboration skills with the ability to work effectively in a team-based environment.

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, 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.

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 o