Apply GMP, validation, and project-management expertise to retire pharmaceutical manufacturing assets and coordinate site conversion work in Ottawa.
This Decommissioning Lead role covers process remediation and execution at a Canadian pharmaceutical contract-manufacturing facility. The site is moving from oral solid dose production toward aseptic liquid filling, requiring disciplined equipment retirement and documentation. You will work with QA, Validation, Engineering, Maintenance, EHS, Facilities, operators, and contractors.
Key Responsibilities: Identify gaps against Health Canada and FDA GMP expectations
Build master plans covering assets, resources, milestones, and schedules
Manage asset-specific change controls and retirement records
Oversee cleaning, decontamination,



and product-contact verification
Coordinate removal activities with current filling construction
Requirements: Degree in Chemical, Mechanical, Process Engineering, or related field
Eight or more years in pharmaceutical or GMP operations
Strong CQV lifecycle and equipment-retirement understanding
Knowledge of ASTM E2500, ISPE, GAMP 5, and FDA requirements
Eligible to work in Canada and available onsite full-time
Bring structured planning, compliance judgment, and stakeholder communication to pharmaceutical asset retirement and aseptic capacity development.

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📌 GMP Equipment Retirement Project Lead (Quebec City)
🏢 Mantu
📍 Quebec City