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 Good 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...