Documentation Specialist
2 weeks ago
We are hiring for our client in the biotechnology industry.
Duration: 4 months (extendable)
Job type: 100% onsite (Monday to Friday)
Pay: $42 to 45/hr on T4 (no benefits)
Duties
- Manage the Quality Management System (QMS) and GMP-critical documentation.
- Oversee document reviews, approvals, and compliance with standards.
- Maintain records of document status, change controls, and approvals.
- Ensure accuracy and traceability of document cross-references.
- Maintain an electronic document library and a QMS document inventory.
- Manage and distribute controlled documents and quality records.
- Coordinate off-site storage and fulfill requests for document copies.
Requirements
- Bachelor’s degree OR high school education with a minimum of 3 years of experience in a GMP-controlled environment.
- Experience implementing document control strategies in a GMP-controlled environment.
- Proficiency with MS Office products and the ability to learn new systems as required.
- Strong communication skills, with the ability to communicate in English.
- Experience using word processing, spreadsheet, and presentation software.
- Experience with Veeva or Magic is a plus.
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