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5.0 - 7.0 years

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bengaluru, karnataka, india

On-site

Job Description Summary Job Description P3-14314 Job Responsibilities: Represents Regulatory Affairs on product development teams to support new product development and change control to ensure US, EU, and other global regulatory requirements are met Evaluates medical device regulations and leads development of global regulatory strategies to bring products to market Reviews and approves design control documentation and product labeling in consideration of US, EU, and other global regulatory requirements Authors FDA submissions, EU technical files, and other regulatory documents for submission to regulatory bodies for product review and approval Leads interactions with FDA, EU notified bodie...

Posted 23 hours ago

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5.0 - 7.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Job Description Summary Job Description P3-14314 Job Responsibilities Represents Regulatory Affairs on product development teams to support new product development and change control to ensure US, EU, and other global regulatory requirements are met Evaluates medical device regulations and leads development of global regulatory strategies to bring products to market Reviews and approves design control documentation and product labeling in consideration of US, EU, and other global regulatory requirements Authors FDA submissions, EU technical files, and other regulatory documents for submission to regulatory bodies for product review and approval Leads interactions with FDA, EU notified bodies...

Posted 1 day ago

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5.0 - 7.0 years

0 Lacs

bengaluru, karnataka, india

On-site

Job Description Summary Job Description P3-14314 Job Responsibilities: Represents Regulatory Affairs on product development teams to support new product development and change control to ensure US, EU, and other global regulatory requirements are met Evaluates medical device regulations and leads development of global regulatory strategies to bring products to market Reviews and approves design control documentation and product labeling in consideration of US, EU, and other global regulatory requirements Authors FDA submissions, EU technical files, and other regulatory documents for submission to regulatory bodies for product review and approval Leads interactions with FDA, EU notified bodie...

Posted 1 day ago

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