Exciting pharmaceutical company has a contract Quality Documentation Specialist Position!
Competitive Pay: Max pays $35/HR NO 1099 OR C2C option
Title: Quality Documentation Specialist
Position type: This will be a 6 month contract with potential for extension
Work Hours: Monday-Friday 8am-5pm-This is an onsite role.
Location: North Billerica, MA
Job Summary:
The Quality Document Coordinator is an individual contributor who is responsible for conducting day to day processing of controlled documents for cGMP operations. Responsible for compliance in accordance with Document Management procedures and will assist with ongoing Quality documentation deliverables driven by business objectives and identified by management.
Must Have Experience:
4+ years of experience in the pharmaceutical or medical devices industry, within Quality or Documentation function
Proficient in advanced functions of Microsoft Word-will be formatting existing documents and new documents to specific requirements
A combination of education, training and experience may be considered in lieu of the above stated qualifications.