Senior Engineer Pharmaceutical Validation

Position: Senior Engineer for Pharmaceutical Validation
Advance your career at LAPORTE as a Senior Engineer specializing in Pharmaceutical Validation in the Greater Toronto Area. This role centers on expert management of validation processes and compliance with GMP.

LAPORTE, an engineering firm celebrated for its 25-year legacy, is looking for a validation specialist with a minimum of five years’ experience.

Your role will encompass drafting critical validation documentation and conducting thorough compliance assessments. Collaborating with clients, you will ensure efficient validation activities in line with industry standards.

Key Responsibilities:

• Create validation master documents and execute protocols

• Oversee equipment/system qualification aligned with GMP

• Support QA teams in addressing compliance deviations

• Manage and maintain relationships with client accounts

• Ensure all validation activities meet regulatory standards

Requirements:

• Degree in science, engineering, or a related field

• At least 5 years of relevant pharmaceutical expertise

• Deep knowledge of Good Manufacturing Practices

• Understanding of manufacturing processes

• Openness to travel to various client sites

Champion your career in validation engineering with you at LAPORTE's dedicated team.
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