Lead pharmaceutical equipment retirement in Ottawa using GMP compliance, CQV expertise, and oral solid dose manufacturing experience onsite full-time.Amaris Consulting seeks a Decommissioning Lead for a Canadian contract-manufacturing site transitioning toward aseptic liquid filling. You will manage process remediation and decommissioning execution while coordinating compliance, equipment retirement, and facility repurposing. The work spans Health Canada and FDA GMP expectations, validation documentation, asset controls, and stakeholder coordination.Key Responsibilities: Strengthen decommissioning frameworks, SOPs, templates, and change controlsDevelop risk-based plans, checklists, and verification documentsLead oral solid dose equipment decommissioning and asset dispositionCoordinate systems retirement, data archiving,



and records retentionReport progress, risks, deviations, and decisions weeklyRequirements: Engineering or Pharmaceutical Sciences degree, or related disciplineAt least 8 years in pharmaceutical manufacturing, engineering, validation, CQV, or GMP operationsHands-on oral solid dose equipment experience through packagingEnd-to-end decommissioning project experienceAvailability for full time onsite work in OttawaApply decommissioning leadership, GMP knowledge, and equipment-retirement expertise to support Amaris Consulting's aseptic expansion project.#J-18808-Ljbffr

📌 Pharmaceutical Decommissioning Lead Ottawa (Quebec City)
🏢 Mantu
📍 Quebec City