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5 + Years in  design controls and working knowledge of medical device regulations and standards (EU Medical Device Regulation, ISO 13485, etc.)

5+ years of experience in the medical device industry

Bachelor’s degree or equivalent preferably in regulatory affairs or science-related field or equivalent experience in the medical device industry

Interfaces with internal stakeholders such as marketing, engineering, research and development, manufacturing, quality, service, and clinical

Interfaces with external stakeholders such as auditors/inspectors, regulatory submission reviewers, notified bodies, and suppliers

To apply for this job email your details to hr@vantage-consulting.solutions