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Validation Manager

Job

Life Technologies (Thermo Fisher Scientific)

Greenville, NC (In Person)

Full-Time

Posted 4 days ago (Updated 2 days ago) • Actively hiring

Expires 7/3/2026

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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 Experience 6+ years of experience in commissioning, qualification, and/or validation within pharmaceutical or regulated manufacturing environments Minimum 3+ years of leadership experience, including managing engineers and/or contractor teams Hands-on experience supporting capital projects, including commissioning and qualification of new equipment and systems in a Steriles Manufacturing facility Experience reviewing and approving technical project plans, validation strategies, and execution approaches Proven ability to manage highly effective teams (FTEs + contractors) and a complex portfolio of concurrent projects Experience collaborating cross-functionally with quality, process engineering, automation, facilities, maintenance, and operations Experience supporting or developing early talent/co-op programs preferred Knowledge, Skills, Abilities Strong understanding of cGMP's and C&Q processes Project and resource management skills Strong leadership and organizational capability Competencies Leadership, Project Management, Collaboration, Accountability, Operational Excellence