Elevate documentation processes as a Quality Control Document Specialist at Roche in Mississauga. Manage electronic documents, ensure compliance, and support quality initiatives in a dynamic environment.

Roche is seeking a Document Specialist with a B.A. or B.S. in Life Science and 3-5 years of cGMP pharmaceutical experience. This role emphasizes your expertise in technical writing, document management, and industry standards like ALCOA+ and ICH guidelines. You will play a crucial role in supporting compliance reviews and documentation-related activities for Network QC.

Key Responsibilities:
• Support Network QC projects and administrative tasks
• Review data and technical documents for compliance
• Manage electronic document lifecycle with Veeva
• Act as a liaison for inspection and event management
• Establish personal goals to meet assignment deadlines

Requirements:
• B.A., B.S., or higher in Life Science or ...