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.