LAPORTE Senior Engineer in Validation

Boost your career trajectory with LAPORTE as a Senior Engineer in Validation. This hybrid position emphasizes compliance and quality assurance through effective validation plan execution.

As a top consulting engineering firm, LAPORTE seeks a skilled Senior Pharmaceutical Validation Engineer with over five years of relevant experience. The ideal candidate should have extensive knowledge of Good Manufacturing Practices (GMP) and the capacity to collaborate with client QA teams, ensuring streamlined validation processes.

Key Responsibilities:

• Draft master validation documents and execute risk analyses

• Conduct equipment and process qualification protocols

• Maintain compliance with GMP throughout the validation lifecycle

• Aid QA teams in change notices and CAPA implementations

• Manage and nurture client accounts effectively

Requirements:

• Bachelor’s or master’s in a relevant field

• At least five years of experience in the pharmaceutical sector

• Strong comprehension of GMP regulations

• Open to traveling for client visits

• Deep understanding of pharmaceutical manufacturing processes

Capitalize on your expertise in validation with LAPORTE's innovative team.
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