Join Thermo Fisher Scientific as a Validation Engineering Specialist I to utilize your validation expertise while adhering to Valuable Manufacturing Practices. This in office position focuses on protocol preparation and compliance verification.

In this role, you will provide specialized validation knowledge essential for operations and client support. Your experience in pharmaceutical processes will guide you in preparing validation protocols, documenting reports, and ensuring adherence to Patheon Standard Operating Procedures. Monitoring manufacturing operations and performing statistical analysis will also be crucial responsibilities in your daily tasks.

Key Responsibilities:
• Prepare validation protocols and reports for various studies
• Coordinate manufacturing execution and training on protocols




• Collect data and conduct statistical analysis
• Monitor cleaning validation swab sampling activities
• Interact with clients and project managers to drive validation efforts

Requirements:
• Post-secondary diploma in Chemistry or Engineering
• Minimum 1 year experience in validation or process engineering
• Robust written and oral communication skills
• Proficiency in statistical analysis
• Ability to multitask and meet deadlines

Leverage your validation skills at Thermo Fisher Scientific and encourage high standards in pharmaceutical practices.
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📌 Validation Specialist At Thermo Fisher Scientific Ontario
🏢 ThermoFisher Scientific
📍 Ontario