Pharmaceutical GMP technical writing leads this independent contractor role in Oakville, Ontario, creating clear documentation for regulated facilities, systems, and processes.
You will collaborate with client engineering, automation, quality, validation, and operations teams. The role focuses on drafting, revising, and coordinating controlled documents for pharmaceutical operations. Strong editing, organization, and attention to detail are essential for user-focused documentation.
Key Responsibilities:
- Draft and revise GMP-compliant controlled documentation
- Develop SOPs for process operations and automation systems
- Prepare process narratives, job aids, and work instructions
- Coordinate document approvals with cross-functional reviewers
- Maintain traceability documentation and consumable lists
Requirements:
- Experience within the pharmaceutical industry
- Strong technical writing and editing skills
- Working knowledge of GMP documentation and document control
- Ability to translate technical information into user-focused documents
- Ability to manage priorities, reviews, and deadlines independently
Apply pharmaceutical documentation expertise to SOPs, GMP records, and controlled process materials in Oakville's engineering workplace.