Specialist, Pharmaceutical Validation Engineer GTA

Join a cutting-edge team as a Pharmaceutical Validation Specialist in the Greater Toronto Area. In this hybrid role, you will oversee validation activities, draft important documents, and ensure compliance with GMP regulations.

In this specialist role, you will manage various validation activities, including the development of master validation documents and executing qualification protocols. You'll also have the opportunity to collaborate with client QA teams and manage client relationships, ensuring operational excellence in compliance practices.

Key Responsibilities:

• Draft key validation documents, including cleaning matrices

• Execute cleaning and process qualification protocols

• Maintain GMP compliance during validation operations

• Collaborate with QA teams on change control issues

• Manage client accounts effectively for enhanced service

Requirements:

• Bachelor’s or master’s degree in science or engineering

• Minimum 5 years in pharmaceutical validation or consulting

• Strong GMP knowledge and application

• Understanding of pharmaceutical production processes

• Ability to travel to client sites as needed

Bring your expertise in pharmaceutical validation to drive compliance and client satisfaction in a hybrid work setting.
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