Temp - Process Science Associate - Cell Bank Inventory Management

Regeneron; Raheen Business Park; On-site; EUR 52,000 - 76,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. seeks an Associate Process Scientist to join the Cell Banking team. The role focuses on on-site cell bank inventory management, transfers, and data-driven investigations to support commercial manufacturing operations.

Responsibilities include maintaining accurate records, contributing to reports, and collaborating with Manufacturing, Quality, and Technical Operations to improve process performance and product quality.

Qualifications

• requires a BS/BA in Life Sciences, Engineering, or related field
• experience in pharmaceutical/biotech manufacturing environment preferred
• knowledge of cGMP regulations desirable
• strong analytical, communication, and problem-solving skills with cross-functional collaboration

Responsibilities

• Support in the inventory management of cell banks on-site
• Schedule of cell bank transfers between departments
• Order and transfer of cell banks into and within on-site inventories
• Support delivery of new solutions to IOPS and contributes to study and report packages
• Assist in root cause analysis of process-related deviations using data-driven rationale
• Participate in cross-functional teams to understand process and operational issues
• Contribute to knowledge-based reports and present findings
• Support safety, cleanliness and compliance of Cell Banking spaces in IOPs Raheen
• Produce and maintain accurate records per site procedures

Skills

Analytical skills

Communication skills

Problem-solving

Education

BS/BA in Life Sciences, Engineering, or related field

Job description

Team: Industrial Operations & Product Supply

Temp - Process Science Associate - Cell Bank Inventory Management

Regeneron is currently seeking an Associate Process Scientist, To join our Process Sciences Cell Banking team.

This role provides an opportunity to support commercial manufacturing operations through process monitoring, data analysis, investigations, and scientific problem-solving. You will collaborate with cross-functional teams to help ensure consistent manufacturing performance and product quality.

When & Where:

• This is an onsite role supporting commercial biopharmaceutical manufacturing operations.
• The position partners closely with Manufacturing, Quality, and Technical Operations teams.
• The role supports process monitoring, investigations, and continuous improvement activities across manufacturing processes.

What You'll Do:

• Support in the inventory management of cell banks on-site
• Schedule of cell bank transfers between departments
• Order and transfer of cell banks into and within on-site inventories
• Support delivery of new solutions to IOPS and contributes to best-in-class study and report packages.
• Assists in root cause analysis of process related deviations using scientific data-driven rationale.
• Participate in cross functional teams to understand process and operational issues associated to the Cell Bank function and associated investigations.
• Contribute to knowledge-based reports summarising conclusion of studies, investigations and process improvements and present findings at group meetings.
• Support the safety, cleanliness and compliance of the Cell Banking spaces in IOPs Raheen.
• Produce and maintains accurate records in accordance with site procedures and guidelines.

The Environment and Physical Rhythms of This Role:

• Thrive in a fast-paced, GMP-regulated manufacturing environment focused on delivering medicines to patients.
• Work across multiple priorities while maintaining strong attention to detail and data integrity.
• Partner with colleagues across Manufacturing, Quality, Engineering, and Process Sciences to solve complex challenges.
• Use scientific and analytical thinking to support process performance, continuous improvement, and operational excellence.

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

• Requires a BS/BA in Life Sciences, Engineering, or a related field; other degree disciplines may be considered with relevant experience.
• Experience working in a pharmaceutical, biotechnology, manufacturing, or related scientific environment is preferred.
• Knowledge of cGMP regulations and regulated manufacturing environments is desirable.
• Strong analytical, communication, and problem-solving skills with the ability to collaborate across teams.

Thrive today. Grow Tomorrow.

#IRELIM #JOBSIEST #LI-Onsite

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.

We take hiring seriously - because finding the right person for our mission matters as much to us as finding the right company matters to you. Our process is thorough by design: we want every new hire to feel confident they've found a place where their work truly matters, and we want to be just as confident we've found someone who'll thrive here. It's a two-way conversation, not a one-way interview.

Part of the team

Where You'll Make an Impact

Here, you'll collaborate with teams across regions to help move our mission forward.

We invest in your health and stability so you can focus on making meaningful impact. Below is a highlight of benefit programs that may be available to you, depending on your country of employment, role, etc.

Life insurance and disability coverage

Global wellness support & benefits access

Paid time off, personal/flexibility hours and holiday leave

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