We are a specialized engineering company with international exposure and subject matter expertise in the design, fabrication and qualification of sterile, high purity and potent containment process equipment and plants.

We offer
a true creative engineering design work environment with a wide range of interesting projects in the bio-pharmaceutical, personal care and food industry. We are seeking an independent engineering contractor to develop clear, accurate, GMP-compliant controlled documentation for pharmaceutical facilities, systems, equipment, and processes in collaboration with client engineering, automation, quality, validation, and operations teams. Working with project and site stakeholders, you will be responsible for drafting, revising, and coordinating the approval of: Master Environmental Monitoring Plan (MEMP)



documentation Master batch records and associated manufacturing instructions Supplier Quality Management System (SQMS) consumable lists Production consumable lists, mappings, and related traceability documentation Strong technical writing, editing, organization, and attention to detail, with the ability to translate engineering, automation, quality, and validation information into explicit user-focused documents. Working knowledge of GMP documentation, document control, and regulated pharmaceutical operations. Experience within the pharmaceutical industry The primary work location will be our Oakville, Ontario office

📌 Technical Writer (Oakville)
🏢 GMP Engineering
📍 Oakville