Staff Engineer - Global Regulatory - Medical Devices in Gurugram at Stryker Corporation

Date Posted: 7/25/2018

Job Snapshot

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Job Description

Working experience of Regulatory submissions such as FDA (IDE/510k/PMA) and EU (CE Technical file and dossier) ​Working experience with R&D teams in regulatory area ​Regulatory Submission knowledge of International is a plus ​Accountable for regulatory strategy and deliverables to support New Product development both domestically and internationally Interaction with cross functional business partners for regulatory guidance ​Proactively assess policies and emerging issues related to Medical Devices and work closely with divisions to develop and implement strategies to address the impact from regulatory perspective ​Good judgement with ability to make timely and sound decisions  ,10-Aug-2018

Work From Home: No

Travel Percentage: None

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