Pharmaceutical Validation Engineer

Responsibilities

• Write validation master documents (e.g., commissioning/validation master plan (VMP), risk analysis, cleaning matrix, user requirements (URS))
• Write and execute qualification protocols for equipment/systems (IQ/OQ/PQ), processes, and cleaning
• Coordinate and ensure GMP compliance during validation activities and general operations
• Support client QA compliance groups in initiating change notices or reporting deviations to initiate CAPA, Change Control, or other relevant actions
• Manage client accounts

Requirements

• Bachelor's or Master's degree in science, engineering, or other relevant disciplines
• Minimum of 2 years of experience in a pharmaceutical environment (plant or consulting)
• Strong knowledge of Good Manufacturing Practices (GMP)
• Knowledge of pharmaceutical manufacturing processes
• Mobility for travel to client sites

Benefits

• Rapid evolution opportunities
• Complete group insurance (medical, dental, vision) starting from day 1
• 3 weeks of regular vacation upon hiring
• 1 week of paid Christmas closure
• 1 additional week of personal leave
• Employer-contributed RRSP (4%)
• OIQ fees paid by Laporte
• Public transit reimbursement
• On-site gym, weight room, and yoga facilities
• Electric vehicle charging stations

About the Company

LAPORTE is a consulting engineering firm providing high-value engineering services to pharmaceutical, agri-food, and industrial biotech plants. The company has 25 agencies across North America and Europe, with over 480 employees.