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 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