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 recent 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.

📌 GMP Equipment Retirement Project Lead (Ahuntsic)
🏢 Mantu
📍 Ahuntsic