Temp - Process Science Associate - Cell Bank Inventory Management

When & Where:

Location: Raheen, Limerick, Ireland. 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.

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 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. 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.

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases. Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company's Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.