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 Valuable 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.#J-18808-Ljbffr

📌 Senior Pharmaceutical Engineer At Laporte (Winnipeg)
🏢 LAPORTE
📍 Winnipeg