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
• Strong computer skills and data knowledge
• Ability to analyze and maintain documentation

Join our team to ensure quality and compliance in our operations at Coquitlam.
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📌 Validation Specialist at Coquitlam Facility (British Columbia)
🏢 Natural Factors
📍 British Columbia