Spec QA DMR
Wuhan 武汉hybrid
Posted yesterday · via Workday
About this role
Job Summary Job Description Collect and review Device Master Record (DMR) documents for Medline products subject to the regulatory requirements and project development plan; Establish inspection criteria of new finished products, update and maintain inspection criteria for existing products on Medline quality management platform (ETQ) Maintain functions of inspection criteria in Medline quality management platform (ETQ) available for inspection Provide training to internal and external stakeholders on the procedure and requirement of DMR and inspection criteria when necessary. Conduct change control by reviewing documents provided by suppliers who have submitted the requests, and assist in helping suppliers complete the changes.…
Read the full description on Medline Industries, LP's site →
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
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2
Level fit
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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 Wuhan 武汉. We weight your proximity and willingness to relocate.
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