Biotech Production Coordinator

Biotech Production Coordinator

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Biotech Production Coordinator I-III to join our Manufacturing team.

In this role, you will support manufacturing operations by coordinating inventory, documentation, production scheduling, sampling activities, and compliance-related processes while partnering with Manufacturing, Quality, Supply Chain, and other cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & Where:

Location: Rensselaer, New York

Shift Requirements: Tues-Fri, 6:00am-4:30pm

Other Requirements: Ability to support manufacturing operations in a regulated manufacturing environment

What You'll Do:

Oversee the lifecycle management of manufacturing documentation.

Prepare routine and non-routine reports and track key performance indicators to support operational goals.

Maintain inventory accuracy through investigations, weekly reviews, reconciliations, and related activities.

Perform and interpret Good Manufacturing Practice (GMP) and Good Practice (GxP) data analysis.

Create and review sampling intake documentation for manufacturing operations.

Coordinate material requirements to help ensure production continuity.

Create and maintain bills of materials to support manufacturing needs.

Evaluate, initiate, and monitor deviations and other compliance-related events.

Coordinate, review, and catalog manufacturing documentation.

Serve as a liaison between Manufacturing and other functional areas to support efficient operations.

The Environment and Physical Rhythms of This Role:

Work in a regulated biopharmaceutical manufacturing environment.

Utilize multiple systems, data sources, calculations, and documentation to support daily operations.

Balance office-based coordination activities with supporting manufacturing operations.

Manage multiple priorities and deadlines in a fast-paced environment.

Collaborate cross-functionally to ensure production and compliance objectives are achieved.

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

Required:

Bachelor's degree or equivalent combination of education and experience.

0-2+ years of related experience.

Strong organizational, communication, and problem-solving skills.

Ability to navigate multiple systems, data sources, calculations, and documentation.

Preferred:

Experience in a Current Good Manufacturing Practice (cGMP) environment.

Experience in Quality Assurance, project management, inventory management, or manufacturing operations.

Experience analyzing data and supporting compliance-related activities.

Thrive Today. Grow Tomorrow.

Student Loan Paydown Program & Tuition Reimbursement

Family Care Benefits

Relocation Assistance

Inclusion, Culture and Well-Being Programs (including physical and mental health)

Does this sound like you? Apply now to take your first step towards living the Regeneron Way!

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! 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.

Salary Range (hourly)

$21.49 - $33.61