Staff Quality Management Systems Specialist (Onsite)
Greciaonsitemid
Posted today · via Workday
About this role
Work Flexibility: Onsite As a Quality Management Systems Specialist, you will support the administration and continuous improvement of document and change control processes within a regulated medical device environment. You will coordinate controlled documentation, quality records, and change activities while partnering with cross-functional teams to maintain compliance with Quality Management System requirements. What you will do • Coordinate document and change control activities, including the release, revision, implementation, and maintenance of controlled documents in electronic systems. • Review quality records for compliance with Good Documentation Practices (GDP), established procedures, and Quality Management System requirements.…
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
This role is mid-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.
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