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
- Transparent technical writing and editing capability

Use technical writing, document control, and cross-functional collaboration to deliver accurate pharmaceutical process documentation and GMP records.

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