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. Solid 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
Robust 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 setting.
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