Medtronic Released Job Openings On 16-12-2021.Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details are provided below. Interested and eligible candidates can submit application along with resume.Â
Vacancy Details:
Medtronic Recruiting B Pharm / M Pharm / Bachelor or masters degree in Bio-Medical Engineering / Science Candidates with 7 to 10 Years experience in Clinical research and Monitoring field for Senior Regulatory Affairs Position.Complete Details for the Senior Regulatory Affairs as follows.
Important Details :
- Location : Gurgaon
- No of Vacancies:01Â
- Details of Salary: NA.
- Opening date for online Application: 16-12-2021
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
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Job Description/Skills Required
- Manage, plan and execute the preparation, review and submission of dossiers for product registrations, import licenses and other approvals from regulatory agencies (registrations and renewals) thereby supporting the business units and supply chain management in compliance with regulatory requirements in India.
- Coordination with global regulatory teams, local BU & other functions, for regulatory strategies and all documentation support required for regulatory submissions in India.
- Submit and track registration/re-registration applications with the authorities.
- Liaise with product divisions and obtain relevant details for filing changes to the approved products/licenses.
- Assess the Change controls from the product divisions through post approval change management and continuously ensure regulatory compliance (reporting of adverse events/field actions, etc.).
- Understanding & interpretation of law & the local regulatory requirement and implementing same in submission with compliance.
- Close monitoring of any changes in local & global regulations and communicating same within the department and respecting & following all SOP / system implemented within the department and organization.
- Ensure business continuity through regulatory filings, obtaining regulatory approvals and continuously ensuring regulatory compliance. Also ensure continuous implementation of the Quality Management System in India.
- Interface and coordinate with regulatory agencies/competent authorities (CDSCO, State FDA, DoT, AERB, etc.) with respect to submissions, obtaining registrations/licenses, amendments, regulatory compliance, packaging, quality control testing or release, etc.
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