Become a Validation Specialist at our Coquitlam location, focusing on validation activities that ensure compliance with regulations and best practices. Engage in exciting projects involving manufacturing and laboratory equipment validation. This contract role involves a variety of responsibilities, from executing validation protocols to coordinating with different departments.

You will oversee validation efforts and ensure that processes align with Valuable Manufacturing Practices and regulatory standards while managing documentation and change controls. Key Responsibilities:
Execute validation protocols for equipment and processes
Coordinate validation projects and schedules
Review key documents and validation reports
Monitor validation master plan progress
Participate in change control evaluations Requirements:
Bachelor's degree in Chemistry or Engineering
Over 2 years in validation roles
Experience in GMP environments
Robust computer skills and data knowledge
Ability to analyze and maintain documentation Join our team to ensure quality and compliance in our operations at Coquitlam.

📌 Validation Specialist At Coquitlam Facility (Canada)
🏢 Natural Factors
📍 Canada