Document Coordinator- Contract (Grand Island, New York)

Retrieve and coordinate the workflow of manufacturing batch records.
Perform tasks within the Quality Systems Document Management function associated with the timely review of manufacturing records and product disposition in the current ERP, laboratory systems and Excel.
Maintain filing of completed batch records.
Assist internal customers in the retrival of batch records.
High attention to detail is required. Professional behavior.
Ability to work independantly as well as part of a team.
Ability to effectively interact with department personnnel and internal customers in a way that enhances department productivity and improves processes.
Ability to communicate both verbally and electronically to satisfy requirements as needed.
Excellent organizational skills required.
Must demonstrate exceptional computer skills with Excel, Word, Access databases and other programs as required.
Must possess self-motivation and a positive attitude.
Education and
High School diploma required.
Associates degree preferred with 2 years experience in related cGMP field, or minimum of 1 year degree in business or technical discipline with 2+ years experience in a role which demonstrates attention to detail wth high standards to error free work.

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