Biotech Production Coordinator

BioSpace; City of Rensselaer (NY); On-site; USD 34,000 - 53,000; Full time

Benefits offered by this job

Annual bonuses

Equity awards

401(k) company match

Health benefits

Wellness programs

Paid time off

Job summary

Regeneron is seeking a Biotech Production Coordinator in Rensselaer, NY, to manage documentation, inventory, sampling, and related records for manufacturing. The role supports GMP/GxP processes and ensures production continuity through effective material coordination.

The position offers a Monday–Friday schedule, 8:00am–4:30pm, with responsibilities spanning documentation lifecycle, KPI tracking, and cross‑functional collaboration to maintain quality and efficiency.

Qualifications

• BS/BA Degree with 0-2+ years of related experience.
• Experience in a cGMP environment or quality assurance is desirable.
• Ability to navigate a variety of systems, data, calculations, and documentation.

Responsibilities

• Oversees lifecycle management of manufacturing documentation.
• Prepare routine and non-routine progress reports and KPI tracking.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and related activities.
• Perform analysis of GMP and GxP data.
• Create and review sampling intake for manufacturing operations and protocols.
• Coordinate material needs to ensure production continuity.
• Ensure systematic bill of materials are created and maintained.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Coordinate, review, and catalogue various manufacturing documents.
• Serve as a liaison between manufacturing and other functions.

Skills

Inventory management

Project management

Data interpretation

GxP knowledge

Education

BS/BA Degree

Job description

Build Our Future Together

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Biotech Production Coordinator to maintain and coordinate inventory, scheduling, sampling, and documentation requirements for manufacturing. Facilitate and coordinate inventory, documentation and perform record- related activities for manufacturing.

When & Where

Location: Rensselaer, New York, United States

Work model: Monday-Friday, 8:00am-4:30pm

Discover Your Role

• Oversees the lifecycle management of documentation.
• Prepare both routine and non-routine progress reports and tracking on various KPIs.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
• Performing and interpreting analysis of GMP and GxP data.
• Create and review sampling intake for all manufacturing unit operations and protocols per the appropriate documentation prior to operators going on the floor (about 20% of the time).
• Coordinate appropriate material needs using varying systems and forms to ensure production continuity.
• Ensuring systematic bill of materials are created and maintained for production needs.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Coordinate, review, and catalogue various types of manufacturing documentation.
• Serves as a liaison between manufacturing and other functional areas as needed.

This Role 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.
• Ability to decipher and navigate a variety of different systems, data, calculations, and documentation.

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
• 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.

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) $24.76 - $38.70