Job Description
Job description
We are seeking an experienced Senior Validation Engineer to support a large-scale pharmaceutical manufacturing expansion project focused on sterile manufacturing operations. This role will play a critical part in validation, environmental monitoring, sterility assurance, and quality oversight activities associated with a new aseptic filling facility and supporting infrastructure.
The successful candidate will provide technical leadership for environmental monitoring validation, isolator qualification, aseptic process simulation studies, and equipment qualification while ensuring compliance with current GMP regulations and industry best practices.
Location
Toronto, ON, Canada (On-site)
Key Responsibilities
Environmental Monitoring & Isolator Validation
Ready to Apply?
Submit your application for Senior Validation Engineer – Sterile Manufacturing & Quality Validation at Amaris Consulting
Apply Now