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.
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