Regulatory Affairs Specialist II

**Work Schedule**

Standard (Mon-Fri)

**Environmental Conditions**

Office

**Job Description**

Role Description :
Divisional role as one of the Regulatory Affairs core team members supporting both manufactured and OEM products for the Business Unit (BU). The IEC arm of Regulatory Affairs (RA) is responsible for facilitating and executing the regulatory strategy defined by the business unit RA leadership. This position assists customers by providing regulatory support for the use of business unit products and services. Also, this position will ensure adherence to the company's established processes, policies, and procedures, as well as external regulatory requirements.

Responsibilities :
• Responsible for execution of Class I, II (or equivalent) medical device product registrations in various countries/geographies, interfacing with the cross-functional teams (Engineering, Operations, Quality, Sales & Registration Agents )
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