Temp - Process Science Associate Manufacturing Support

Regeneron Ireland; Limerick; On-site; EUR 50,000 - 75,000; Full time

Job summary

Regeneron Ireland is seeking an Associate Process Scientist, Manufacturing Support to assist commercial biopharmaceutical manufacturing operations. The role focuses on process monitoring, data analysis, investigations, and scientific problem-solving across cross-functional teams to ensure product quality and consistent performance.

The position is onsite at Raheen, Limerick, Ireland, working with Manufacturing, Quality, and Technical Operations to drive process improvements and data-driven

Qualifications

• 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

Responsibilities

• Support manufacturing processes through data analysis, troubleshooting, and scientific investigations
• Author and review protocols, reports, and manufacturing support documentation
• Investigate process-related events including OOS and OOL in-process control results
• Analyze and present process performance data to support decision-making and continuous improvement
• Collaborate with cross-functional teams on risk assessments and technology transfer activities

Job description

Regeneron is currently seeking an Associate Process Scientist, Manufacturing Support to join our Process Sciences 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:

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 manufacturing processes through data analysis, troubleshooting, and scientific investigations.
• Author and review protocols, reports, product impact assessments, and manufacturing support documentation.
• Investigate process-related events, including out-of-specification (OOS) and out-of-limit (OOL) in-process control results.
• Analyze and present process performance data to support decision-making and continuous improvement initiatives.
• Collaborate with cross-functional teams on risk assessments, technology transfer activities, and manufacturing support projects.

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.

Regeneron is 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.

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
• 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.

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.

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.