Support pharmaceutical facility documentation from the Oakville office as an independent contractor with technical writing and GMP knowledge.
This engineering documentation assignment covers facilities, systems, equipment, and processes. You will work with project and site stakeholders across engineering, automation, quality, validation, and operations. Success requires organized document management, accurate editing, and effective collaboration with subject matter experts.
Key Responsibilities: Develop controlled documents for pharmaceutical facilities and systems
Draft master environmental monitoring plan documentation
Prepare master batch records and manufacturing instructions
Complete system and equipment criticality assessments
Coordinate revisions and approval cycles across stakeholders
Requirements: Pharmaceutical industry experience
Knowledge of regulated pharmaceutical operations
Solid organization and attention to detail
Effective collaboration with cross-functional reviewers
Independent management of multiple documents and deadlines
Bring structured technical writing and GMP documentation skills to pharmaceutical facility projects, stakeholder reviews, and approval coordination.