IVD Quality & Regulatory Lead – Global Compliance

L7

software placement groupWebster, TXyesterday
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.
Apply now
Apply now

Level

ManagerL7

Location

Webster, TX

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

To get sharper similar jobs, create your profile using the link below.

Create profile