Senior Pharmaceutical Validation Engineer (Edmonton)

Drive pharmaceutical validation success with LAPORTE as a Senior Pharmaceutical Validation Engineer in Greater Edmonton. With a minimum of 5 years experience, manage critical validation tasks ensuring compliance and efficiency.

Key Responsibilities

• Draft master validation documents for projects
• Execute equipment/system qualification protocols
• Ensure compliance with GMP throughout validation work
• Support clients’ QA teams with necessary reports
• Manage client accounts effectively

Requirements

• Bachelor’s or master’s degree in science or engineering
• At least 5 years of pharmaceutical industry experience
• Solid knowledge of GMP regulations
• Familiarity with manufacturing processes
• Willingness to travel to client sites

Utilize your expertise in validation and quality assurance to enhance pharmaceutical processes at LAPORTE.