Senior Validation Engineer at LAPORTE

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 experience in the pharmaceutical sector

• Strong understanding of GMP and manufacturing processes

• Willingness to travel to client locations

• Proven ability to manage projects successfully

Advance your expertise in validation engineering with LAPORTE's dynamic team culture.
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