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Regeneron Pharmaceuticals Manufacturing Document Associate in Rensselaer, New York

Summary: Facilitate and coordinate inventory, documentation and perform record- related activities for manufacturing.

Please note that this shift is 3rd, Sunday-Thursday, from 10:00 p.m.-8:30 a.m.

Essential Duties and Responsibilities include, but are not limited to, the following:

  • Facilitate and catalogue manufacturing documentation, manufacturing records and batch sheets.

  • Coordinate document movement across all functional groups.

  • Prepare routine progress reports on manufacturing documentation for management.

  • Responsible for ensuring documentation timelines are met through effective communication and follow through with document owners.

  • Ensure accurate system inventory is maintained through the performance inventory reconciliations, facilitation of material delivery review, and other related activities.

  • Review and approve bills of materials, sample studies and other manufacturing documentation as needed.

  • Serves as a liaison between manufacturing and other functional areas as needed.

Education and Experience:

Requires Associate’s Degree with 0-2+ years of related experience; will substitute relevant experience for education. Experience in a cGMP environment, quality assurance, project management, or inventory management desired.