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 Good 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.
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