Junior Associate- Regulatory Affairs

4 weeks ago


Delhi, India MED-EL India Privated Ltd Full time

**Experience: 1-2-year Experience in Medical devices (Fresher with interest in Medical devices may also apply)**

**Location: Delhi/ gurgaon**

**Qualifications: B. Pharmacy**

**Job Profile**:

- Regulatory and Quality Assurance for India Sub-continent to support the continuous development, implementation and maintenance of the company’s quality management system and regulatory affairs strategies & submissions.
- Support Internal/External Audits and distributor audits, issue audit reports, follow up on responses, CAPAs and close out internal/distributor audit.
- Manage, plan & execute the preparations, review and submission of dossiers for product registrations, import licenses and other approvals from regulatory agencies (registrations, re-registration and renewals) & line extension indications and labelling approvals of medical devices.
- Manage & execute Head office plan on any Change notification which will require Post Approval Change in India.
- BIS registration for imported electronic and other equipment as per CRS scheme
- Maintain PMS Data and ensure timely reporting of adverse events & Field safety corrective actions to regulatory agencies.
- Responsible for Query resolving raised by DCGI, BIS, WPC, Legal Metrology, Customs or ADC port.
- Coordination with our Head Office and other global regulatory teams for regulatory strategies and all documentation support required for regulatory submissions in Indian sub-continent.
- Supporting the Sales Teams on tender related issues/Documentation.

**Salary**: ₹15,000.00 - ₹30,000.00 per month

Schedule:

- Fixed shift

Ability to commute/relocate:

- Delhi - Delhi, Delhi: Reliably commute or planning to relocate before starting work (required)

**Experience**:

- total work: 1 year (required)
- Regulatory affairs: 1 year (required)
- medical device regulatory: 1 year (required)



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