Document QA/Copyeditor

Found in: Appcast Linkedin GBL C2 - 2 weeks ago

Hopewell, United States GroupA Full time

We are looking for a Document QA/Copyeditor to join our team in Hopewell, NJ. In this role, you will assist with site documentation needs ensuring GMP compliance of day-to-day operations.


Responsibilities:

  • Support Document Control Team with the formatting of procedural and technical documents, MBRs, and other GMP related documents
  • Process documents through the Veeva Quality Management System according to corporate and site procedures
  • Manage and track a large number of documents to completion
  • Undertake any other duties, either for this department or any other department within the business, which may be requested by the Line Manager, for which training and/or an explanation has been provided and understood


Requirements:

  • General GMP knowledge
  • Exceptional organizational and time management skills a must
  • Experience using Quality Management System(s) such as Veeva Vault
  • Exceptional knowledge of Microsoft Word including shortcuts and formatting tools
  • Excellent attention to detail, with the ability to work accurately in a busy and demanding environment
  • Strong collaboration and communication skills
  • Ability to successfully work within strict timelines

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