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Senior Validation Engineer at LAPORTE
Description
Elevate your career with LAPORTE as a Senior Validation Engineer focusing on pharmaceutical compliance in the Greater Toronto Area. This role emphasizes expertise in validation protocols and Good Manufacturing Practices.
Join LAPORTE, a consulting firm with over 25 years in pharmaceutical engineering. The ideal candidate boasts at least five years of experience in validating pharmaceutical equipment and managing documentation. You will play a key role in drafting validation master plans and ensuring compliance with GMP standards during validation operations.
Key Responsibilities:
• Draft master validation documentation such as VMP and risk analysis
• Execute qualification protocols including IQ/OQ/PQ
• Ensure compliance with GMP during all validation activities
• Support client QA teams with change notices and deviations
• Manage client accounts effectively
Requirements:
• Bachelor’s or master’s degree in a relevant discipline
• Minimum 5 years of experien...
Join LAPORTE, a consulting firm with over 25 years in pharmaceutical engineering. The ideal candidate boasts at least five years of experience in validating pharmaceutical equipment and managing documentation. You will play a key role in drafting validation master plans and ensuring compliance with GMP standards during validation operations.
Key Responsibilities:
• Draft master validation documentation such as VMP and risk analysis
• Execute qualification protocols including IQ/OQ/PQ
• Ensure compliance with GMP during all validation activities
• Support client QA teams with change notices and deviations
• Manage client accounts effectively
Requirements:
• Bachelor’s or master’s degree in a relevant discipline
• Minimum 5 years of experien...