Senior Validation Manager - GMP Compliance & Qualification
Job in
Bedford, Cuyahoga County, Ohio, 44146, USA
Listed on 2026-09-07
Listing for:
RXinsider LTD.
Full Time
position Listed on 2026-09-07
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager, Quality Engineering -
Pharmaceutical
Regulatory Compliance Specialist, Quality Engineering
Job Description & How to Apply Below
Hikma Pharmaceuticals USA Inc. in Bedford, OH, is seeking a Sr. Validation Manager to lead validation activities for CGMP-compliant processes and equipment. You will manage VMPs, IQ/OQ/PQ, URS review, and cross-functional coordination across Operations, Engineering, Quality Control and Quality Assurance.
The role requires 8–10 years’ validation experience in pharma, a technical degree, plus strong documentation and problem-solving skills. A robust benefits package is offered.
#J-18808-LjbffrPosition Requirements
10+ Years
work experience
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(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).
(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).
Search for further Jobs Here:
×