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 controls

Develop risk-based plans, checklists, and verification documents

Lead oral solid dose equipment decommissioning and asset disposition

Coordinate systems retirement,



data archiving, and records retention

Report progress, risks, deviations, and decisions weekly

Requirements: Engineering or Pharmaceutical Sciences degree, or related discipline

At least 8 years in pharmaceutical manufacturing, engineering, validation, CQV, or GMP operations

Hands-on oral solid dose equipment experience through packaging

End-to-end decommissioning project experience

Availability for full-time onsite work in Ottawa

Apply decommissioning leadership, GMP knowledge, and equipment-retirement expertise to support Amaris Consulting's aseptic expansion project.

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