Elevate your career with LAPORTE as a Senior Pharmaceutical Engineer specializing in validation. This role focuses on key activities that ensure compliance and operational excellence.
LAPORTE, a leader in consulting engineering with 25 years in the industry, is on the lookout for a Senior Engineer with significant validation experience. You should have at least five years of relevant expertise, particularly in managing validation activities and adhering to Positive Manufacturing Practices (GMP). Experience a supportive work culture that fosters professional development and work-life balance.
Key Responsibilities:
• Create and manage master validation plans
• Carry out equipment and cleaning qualification protocols




• Ensure compliance with GMP throughout processes
• Assist clients with quality assurance and change control
• Oversee client relationships effectively
Requirements:
• Bachelor’s or master’s degree in relevant fields
• 5+ years within the pharmaceutical industry
• In-depth knowledge of GMP
• Familiarity with manufacturing processes
• Willingness to travel as required
Apply your validation knowledge to advance LAPORTE's mission in the pharmaceutical field.
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📌 Senior Pharmaceutical Engineer at LAPORTE (Edmonton)
🏢 LAPORTE
📍 Edmonton