Biotech Production & Documentation Specialist

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

Job summary

Regeneron Pharmaceuticals, Inc. seeks a Biotech Production Coordinator in Rensselaer, NY. The role coordinates inventory, sampling, and documentation for manufacturing, ensuring accuracy and continuous production flow.

The position requires 0–2+ years in a related field, experience in cGMP environments, and strong data analysis capabilities to support GMP/GxP processes on-site. Monday–Friday, standard daytime hours with a focus on manufacturing traceability.

Qualifications

• BS/BA degree with 0–2+ years of related experience in manufacturing or similar.
• Experience in a cGMP environment, quality assurance, project management, or inventory management.
• Ability to decipher and navigate a variety of different systems, data, calculations, and documentation.

Responsibilities

• 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.

Skills

GMP experience

Education

BS/BA Degree

Job description

Regeneron Pharmaceuticals, Inc. seeks a Biotech Production Coordinator in Rensselaer, NY. The role coordinates inventory, sampling, and documentation for manufacturing, ensuring accuracy and continuous production flow.

The position requires 0–2+ years in a related field, experience in cGMP environments, and strong data analysis capabilities to support GMP/GxP processes on-site. Monday–Friday, standard daytime hours with a focus on manufacturing traceability.