GMP Validation Leader: Qualification & CSV Expert
Listed on 2026-10-06
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Katalyst CRO is seeking an experienced Senior Validation Specialist to lead qualification and validation activities in a GMP-regulated environment. You will plan, execute, review, and approve validation documentation for equipment, facilities, processes, and computerized systems while ensuring compliance with FDA, EMA, and cGMP regulations.
Responsibilities include leading DQ/IQ/OQ/PQ lifecycle, authoring validation documents, managing deviations and CAPAs, and collaborating with Quality
The GMP Validation Leader:
Qualification & CSV Expert role at Katalyst CRO is now open for applications in Frederick, MD, United States.
Step into the GMP Validation Leader:
Qualification & CSV Expert role at Katalyst CRO in Frederick, MD, United States and grow with us.
Please review the full job details above before applying.
If your experience matches this role, we encourage you to apply.
All applications are reviewed carefully by our team.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).