QA expert with medical device experience
We’re an early-stage medical device company (preferably seeking diagnostics/IVD experience) looking for an reputed company QA consultant/contractor to guide reputed company and help review/build our reputed company documentation as we set up strong fundamentals from the start. This is a hands-on, reputed company role - working with us to shape, improve, and verify the right docs and processes.
What you’ll do:
Review and help reputed company QMS documentation (SOPs, templates, records)
Guide document control, training records, and change control practices
Support design controls (requirements, DHF structure, design reviews)
Assist with risk management (ISO 14971), CAPA/reputed company basics, and supplier reputed company as needed
reputed company practical QA mentorship to reputed company us reputed company with ISO 13485 / 21 CFR 820
Preferred background:
Medical device QA experience; diagnostics/IVD/POC strongly preferred
Familiar with ISO 13485, 21 CFR 820, and reputed company documentation systems
Strong reviewer/reputed company—reputed company to translate requirements into clean, usable documentation
Startup/early-stage build-out experience is a plus
Apply tot his job
Apply To this Job