Validation Manager
Thermo Fisher Scientific · Greenville, North Carolina, US
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful wor...
Job description
Work Schedule Standard (Mon-Fri) Environmental Conditions: Office Job Description: As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale... About the Business: Join our Pharma Services Group (PSG)—a global leader providing integrated drug development and manufacturing solutions to pharmaceutical and biotech companies. Our Greenville, North Carolina site specializes in sterile and oral solid dose (OSD) manufacturing. Discover Impactful Work: The Validation Manager (C&Q) will lead commissioning and qualification activities across the site, ensuring successful execution of capital projects and operational readiness. A Day in the Life: - Lead ~6 direct reports and ~25 contractors - Manage commissioning & qualification (C&Q) activities - Review and approve capital project requests - Allocate resources and manage workload across projects - Support equipment implementation and startup - Mentor team members and develop co-op pipeline - Collaborate cross-functionally across site functions Keys to Success: Education: - Bachelor’s degree in Engineering, Science, Chemistry, Biology, or related technical discipline Experienc...