Quality Assurance Specialist – GMP, FDA Liaison & Projects
Listed on 2026-10-11
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Quality Assurance - QA/QC
Data Analyst -
Healthcare
Hikma Pharmaceuticals USA Inc. in Bedford, Ohio, is seeking a Quality Assurance Associate to perform field QA activities, including in-process checks, AQL inspections, and batch record reviews. You will ensure GMP compliance and support final product release with guidance to manufacturing staff.
The role requires strong QA background, experience with regulatory audits, and ability to write/ revise SOPs and forms. Onsite work and collaboration with cross-functional teams are essential.
Join us at Hikma as our next Quality Assurance Specialist – GMP, FDA Liaison & Projects in Bedford, OH, United States.
We invite applications for the Quality Assurance Specialist – GMP, FDA Liaison & Projects position located in Bedford, OH, United States.
The following opening is for a Quality Assurance Specialist – GMP, FDA Liaison & Projects with Hikma.
Our team is growing, and we are hiring a Quality Assurance Specialist – GMP, FDA Liaison & Projects in Bedford, OH, United States.
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