What are the responsibilities and job description for the Quality Assurance Contractor position at Planet Pharma?

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

Salary : $35 - $50

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