- Greenville, North Carolina, United States
- On-site
- Full-time · Staff
- 6+ years
As a Staff Validation Engineer, you'll lead validation activities for critical systems, equipment, and processes that enable the development and manufacturing of therapies.
Responsibilities
- Lead validation activities for critical systems, equipment, and processes
- Develop and implement comprehensive validation strategies aligned with regulatory requirements and corporate standards
- Collaborate with cross-functional teams to ensure successful qualification of facilities, utilities, manufacturing equipment, and computerized systems
- Maintain compliance and drive continuous improvement
- Serve as a technical subject matter expert during audits and investigations
Requirements
- Advanced Degree plus 6 years of experience
- Bachelor's Degree plus 8 years of experience
- Engineering
- Science
- Biotechnology