Document QA/Copyeditor

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