Manufacturing Document Associate
- Employer
- Regeneron Pharmaceuticals, Inc.
- Location
- Rensselaer, New York
- Posted
- Jan 22, 2022
- Ref
- REGEA0026R6295
- Discipline
- Manufacturing & Production, Manufacturing/Mechanical
- Hotbed
- Best Places to Work, Pharm Country
- Required Education
- High School or equivalent
- Position Type
- Full time
We are currently recruiting for a Manufacturing Document Associate who will facilitate and coordinate inventory, documentation and perform record- related activities for manufacturing.
As a Manufacturing Document Associate, a typical day might include the following:
Facilitating and cataloging manufacturing documentation, manufacturing records and batch sheets.
Coordinating document movement across all functional groups.
Preparing routine progress reports on manufacturing documentation for management.
Responsible for ensuring documentation timelines are met through effective communication and follow through with document owners.
Ensuring accurate system inventory is maintained through the performance inventory reconciliations, facilitation of material delivery review, and other related activities.
Reviewing and approving bills of materials, sample studies and other manufacturing documentation as needed.
Serving as a liaison between manufacturing and other functional areas as needed.
To be considered for this role we would require; Level I - HS diploma/GED/Leaving Cert; 0-2 yrs experience. College degree may be preferred. Level II - HS diploma/GED/Leaving Cert; 2+ yrs experience. College degree may be preferred. Level III - HS diploma/GED/Leaving Cert; 4+ yrs experience. College degree may be preferred. Level IV - HS diploma/GED/Leaving Cert; 6+ yrs experience. College degree may be preferred. Experience in a cGMP environment, quality assurance, project management, or inventory management desired.
Level is determined based on relevant education and experience.