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 career 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 effectivelyRequirements:
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 requiredApply your validation knowledge to advance LAPORTE's mission in the pharmaceutical field.#J-18808-Ljbffr