Staff Quality Engineer (Onsite)
Greciaonsitestaff
Posted today · via Workday
About this role
Work Flexibility: Onsite As a Quality Engineer, you will support Quality Assurance activities within a regulated medical device environment, partnering with Manufacturing, Research & Development, Regulatory, and Engineering teams. You will monitor product and process quality, investigate nonconformances, manage quality data, and support compliance with FDA Quality System requirements, ISO 13485, and the Medical Device Single Audit Program (MDSAP). What you will do • Investigate product and process quality issues with cross-functional teams, performing risk assessments, historical record reviews, nonconformance evaluations, and corrective action activities.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: teams
2
Level fit
This role is staff-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Grecia. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
teams
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