Job Description:

Managing regulatory submissions (new and renewals) in compliance with local country requirements and ensuring timely registration approval to guarantee compliant market accessProviding advisory support to marketing, sales, operations and other company stakeholders, among all Envista OpCos from a medical device registration management perspectiveTracking and following-up registrations in a timely manner to ensure deadlines are metHelp monitor regulatory trends and changes with relevant contacts, maintain current knowledge base of existing and emerging regulations and standards.

Job Requirements:

Qualifications:

Native Turkish speaker, English fluency in written and spoken is a mustBachelor's degree in Chemistry, Biology, or a related life science fieldStrong attention to detail and organizational skillsExcellent communication and interpersonal skillsAbility to work effectively in a team environment

Preferred knowledge & experience

Knowledge of Turkish medical device regulationsKnowledge/experience of Product Tracking System (ÜTS) registrationsFamiliarity with EU’s and/or FDA’s medical device regulatory requirements

Operating Company:

DEXIS

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