Biotech Production & Documentation Coordinator

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

Job summary

Regeneron Pharmaceuticals in Indiana is seeking an inventory and documentation coordinator for manufacturing operations. The role ensures accurate inventory records, prepares reports, and coordinates material needs to sustain production.

You will manage documentation lifecycle, review sampling intake, and liaise across manufacturing and QA to maintain compliance in a cGMP environment. This on-site position follows a Monday–Friday schedule.

Qualifications

• 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.

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.
• 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

System navigation

Education

Bs/BA Degree

Job description

Regeneron Pharmaceuticals in Indiana is seeking an inventory and documentation coordinator for manufacturing operations. The role ensures accurate inventory records, prepares reports, and coordinates material needs to sustain production.

You will manage documentation lifecycle, review sampling intake, and liaise across manufacturing and QA to maintain compliance in a cGMP environment. This on-site position follows a Monday–Friday schedule.