IVD Quality & Regulatory Lead – Global Compliance
software placement groupWebster, TX
IVD Quality & Regulatory Lead – Global Compliance
software placement groupWebster, TX
today
Industries
Electromedical and Electrotherapeutic Apparatus ManufacturingBiological Product (except Diagnostic) ManufacturingIn-Vitro Diagnostic Substance ManufacturingAbout the role
Software Placement Group is seeking a hands-on Quality and Regulatory Manager to lead QA/RA for IVD products, overseeing QMS, regulatory submissions, and audits across manufacturing, R&D, and commercial activities.
The role requires a Bachelor's in life sciences or related field and 5+ years of QA/RA experience, with strong knowledge of FDA 21 CFR 820, ISO 13485, IVDR/IVDD, and proven track record in regulatory submissions, CAPA, and process validation.
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JOB OVERVIEW
Experience level
Manager
Location
Webster, TX
Occupation
Regulatory Affairs Managers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
Posted
today
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