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
- Strong 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.
Pharmaceutical Facilities Documentation Contractor in Oakville employer: GMP Engineering Inc.
As a Junior Process Engineer at our Oakville, ON office, you'll join a dynamic and collaborative engineering team dedicated to innovation in the pharmaceutical industry. We pride ourselves on fostering a supportive work culture that emphasizes professional growth, offering mentorship from experienced engineers and opportunities for international travel that enrich your career experience. With a commitment to excellence and a focus on GMP-compliant processes, we provide a rewarding environment where your contributions truly matter.
