3+ years experience in quality or regulatory function
Fluency in english required
This role is part of a transformational journey to elevate the Quality Management System across Medical Devices and Consumer Products
Job Summary
This role is part of a transformational journey to elevate the Quality Management System across Medical Devices and Consumer Products.
You will execute post-market surveillance activities including complaint assessment, investigation, and reportability determination primarily for EMEA and Israel markets.
Candidates must be authorized to work in the Czech Republic with no relocation support provided for this on-site position at the Jaroměř mill.
Matching Summary
This role is part of a transformational journey to elevate the Quality Management System across Medical Devices and Consumer Products.
Skills & Requirements
Must-have
Bachelor's degree in science or engineering
3+ years experience in Quality or Regulatory function
Fluency in English required
Experience with complaint assessment and investigation
Knowledge of EMEA / Israel market regulations
Nice-to-have
Multi-language skills advantageous
Experience in regulated industries like cosmetics
Familiarity with medical terminology
Collaborative cross-functional partnership skills
Key Requirements
Bachelor's degree in science, engineering, or related discipline
3+ years broad experience in Quality, Manufacturing, Research & Engineering, or Regulatory function
Must already be authorized to work in the Czech Republic
Work Rights
Must already be authorized to work in the Czech Republic