Biotech Production Coordinator

Regeneron Pharmaceuticals, Inc.; Limerick; On-site; EUR 20,000 - 31,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. in Limerick seeks a Biotech Production Coordinator to join the Manufacturing team. The role focuses on coordinating documentation, maintaining inventory accuracy, and acting as a liaison across functions to uphold schedules.

The position requires a BS/BA and 0-2+ years in a related field, with GMP/GxP experience and potential to train staff and lead cross-functional projects.

Qualifications

• 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.

Responsibilities

• 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 systems, data, calculations, and documentation.
• Ensure timelines are met through effective communication with task/project owners.
• Perform 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 manage projects independently and with cross-functional teams.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Maintain accurate systems related to Manufacturing operations; OPM, MES, LIMS, WMT, FMP, etc.

Education

BS/BA Degree

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.
• Serves 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.

Salary and benefits:

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
• 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.

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.

Other requirements:

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.

Salary Range (hourly):

€14.55 - €22.73