Global Quality & Regulatory Manager (MDR/ISO 13485)

Rotterdam Innovation City

Netherlands

On-site

EUR 70,000 - 110,000

Full time

14 days+
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Job description

Responsibilities

As a Quality Manager you are responsible for the quality assurance and regulatory compliances. You monitor the quality of our products day-to-day and implement guidelines and improvement regularly.

Regulatory Requirements

For EU market, Medical device regulation (MDR) and ISO 13485 are the key to follow. Other regulatory requirements must be complied when entering new market such as US market.

Software Tools

Matrixreq and Odoo ERP are the main software tools we use to ensure quality.

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