Biotech Production Coordinator

Regeneron Ireland; Limerick; On-site; EUR 20,000 - 31,000; Full time

Job summary

Regeneron Ireland is seeking a Biotech Production Coordinator to join our Manufacturing team in Limerick. The role focuses on coordinating documentation, maintaining inventory, and facilitating cross-functional collaboration to ensure timely manufacturing operations.

This position requires a BS/BA degree with 0-2+ years of related experience, preferably with exposure to cGMP environments, QA, project management, or inventory systems.

Qualifications

• BS/BA degree required for role.
• 0-2+ years of related experience or equivalent.
• Experience in a cGMP environment, quality assurance, project management, or inventory management desired.

Responsibilities

• Coordinate, review, and catalogue manufacturing documentation.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and related activities.
• Serve as liaison between manufacturing and other functional areas as needed.
• Navigate systems, data, calculations, and documentation.
• Ensure timelines are met through effective communication with task/project owners.
• Analyze GMP and GxP data.

Skills

GMP knowledge

Communication

Problem solving

Education

BS/BA Degree

Tools

LIMS

OPM

MES

FMP

Job description

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Biotech Production Coordinator to join our Manufacturing team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & Where

Location: Limerick Days: Monday to Friday

What you'll do

• Coordinate, review, and catalogue various types of manufacturing documentation.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
• Serve as a liaison between manufacturing and other functional areas as needed.
• Navigate a variety of different systems, data, calculations, and documentation.
• Responsible for ensuring timelines are met through effective communication and follow through with task and/or project owners.
• Performing analysis of GMP and GxP data.
• Review and approve bills of materials, sample studies, and other manufacturing documentation as needed.
• Extended functional, industry and regulatory knowledge.
• Act as a qualified trainer for new and existing employees.
• Lead and solves technical problems by using expert critical thinking skills and verbal and written communication skills.
• Lead and manages projects independently and with cross-functional teams.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Ensure accurate systems are maintained related to Manufacturing operations; OPM, MES, LIMS, WMT, FMP, etc.

The environment and physical rhythms of this role

• You enjoy working in a team that brings out the best in each other
• You can adhere to the letter and spirit of policies and regulations
• You can adapt to a changing environment and have the ability to adhere to a schedule

Let's find out if we're a fit

• Requires BS/BA Degree with 0-2+ years of related experience or equivalent combination of education and experience.
• Experience in a cGMP environment, quality assurance, project management, or inventory management desired.
• Thrive today.
• Grow tomorrow.

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.

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.

Salary Range (hourly) €14.55 - €22.73

If you have any questions, please speak with your recruiter.

For jobs in Canada: this posting is for an existing position.

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.