QA Document Coordinator

Job Title:	QA Document Coordinator

Duties:	Assist with site documentation needs ensuring GMP compliance of day-to-day operations. 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. 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
Skills:	General GMP knowledge Organizational and time management skills a must Experience with using Quality Management System(s) such as Veeva Vault Advanced 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