Create GMP-compliant process documentation for pharmaceutical operations in Oakville, Ontario, translating automation and validation information clearly.
As an independent engineering contractor, you will develop user-focused documentation with project and site stakeholders. Your work will support process operations, automation systems, manufacturing instructions, and consumable traceability. The assignment requires technical writing strength, document control knowledge, and careful coordination.
Key Responsibilities: Write SOPs for process operations and automation systems
Develop operating descriptions and process narratives
Prepare production consumable mappings and traceability documents
Compile Supplier Quality Management System consumable lists




Revise documents through coordinated review cycles
Requirements: Experience working within the pharmaceutical industry
Working knowledge of GMP documentation requirements
Understanding of document control practices
Ability to organize multiple priorities independently
Explicit technical writing and editing capability
Use technical writing, document control, and cross-functional collaboration to deliver accurate pharmaceutical process documentation and GMP records.

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📌 GMP Process Documentation Specialist (Ontario)
🏢 GMP Engineering
📍 Ontario