$35 - $50 per hr - based on experience level
5 month extendable CONTRACT
Onsite - Hopewell, NJ
Role:
- 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.
- 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:
- Minimum Associates Degree
- 2+ years of QA experience within a biotech or pharma company
- General GMP experience within a pharma or biotech company
- Experience using Quality Management System(s) such as Veeva Vault
- Exceptional organizational and time management skills a must
- 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