Document Control Specialist

Bristol Myers Squibb
Indianapolis, IN
Category Healthcare
Job Description
Bristol Myers Squibb is seeking a Document Control Specialist to oversee and maintain document control systems for a new Radiopharmaceutical facility in Indianapolis. This role involves reviewing GxP controlled documents, managing workflows, ensuring compliance, and coordinating with other departments. The position supports clinical development and GMP commercial operations.

Requirements

  • Manage the process for creation, review, approval, and issuance of GxP controlled site documents.
  • Manage electronic document management system (EDMS) document lifecycle workflows.
  • Review format and metadata of new documents.
  • Provide guidance to document initiators, owners, and users.
  • Coordinate and liaise with other departments.
  • Ensure compliance to training program.
  • Process DCR packages and review for correctness.
  • Create, assign, and archive QA controlled lab notebooks.

Benefits

  • Medical, pharmacy, dental and vision care
  • Wellbeing support
  • Financial well-being resources
  • 401(K)
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