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 expectationsBuild master plans covering assets, resources, milestones, and schedulesManage asset-specific change controls and retirement recordsOversee cleaning, decontamination,



and product-contact verificationCoordinate removal activities with recent filling constructionRequirements: Degree in Chemical, Mechanical, Process Engineering, or related fieldEight or more years in pharmaceutical or GMP operationsStrong CQV lifecycle and equipment-retirement understandingKnowledge of ASTM E2500, ISPE, GAMP 5, and FDA requirementsEligible to work in Canada and available onsite full-timeBring structured planning, compliance judgment, and stakeholder communication to pharmaceutical asset retirement and aseptic capacity development.#J-18808-Ljbffr

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