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3 Job openings at MED-EL India Privated Ltd
Junior Associate-Regulatory Affairs

Nehru Place, Delhi, Delhi

1 years

INR 0.2 - 0.3 Lacs P.A.

On-site

Full Time

Opening with reputed MNC Medical Device Company for regulatory affairs domain. Position: Junior Associate- Regulatory Affairs Qualification: B.Pharmacy Location: Delhi NCR Job Profile: · Good Knowledge of Microsoft Excel and Microsoft office for maintaining import database and shipping documentation. · Supporting the Sales Teams on tender related issues/Documentation. · Support Import & logistics team and regulatory team in various work assigned · Manage, plan & execute labelling approvals of medical devices and accessories including labelling monitoring as per BIS and Legal Metrology and any other regulatory compliances that may become mandatory or statutory in the future. · Preparation, Scrutiny of documents, compilation, submission, follow ups for registration/ re-registration/ renewal applications · Maintain PMS Data and ensure timely reporting of adverse events & Field safety corrective actions to regulatory agencies while Maintaining Cochlear Implant Flow Data (IF) and Implant Traceability. · Perform Internal audit and issue audit reports, follow up on responses, CAPAs and close out internal audit. Interested candidates can share their resume on [email protected] Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Schedule: Day shift Monday to Friday Ability to commute/relocate: Nehru Place, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: regulatory affairs: 1 year (Required) Language: English (Required) Work Location: In person

Junior Associate-Regulatory Affairs

India

1 years

INR 0.2 - 0.3 Lacs P.A.

On-site

Full Time

Opening with reputed MNC Medical Device Company for regulatory affairs domain. Position: Junior Associate- Regulatory Affairs Qualification: B.Pharmacy Location: Delhi NCR Job Profile: · Good Knowledge of Microsoft Excel and Microsoft office for maintaining import database and shipping documentation. · Supporting the Sales Teams on tender related issues/Documentation. · Support Import & logistics team and regulatory team in various work assigned · Manage, plan & execute labelling approvals of medical devices and accessories including labelling monitoring as per BIS and Legal Metrology and any other regulatory compliances that may become mandatory or statutory in the future. · Preparation, Scrutiny of documents, compilation, submission, follow ups for registration/ re-registration/ renewal applications · Maintain PMS Data and ensure timely reporting of adverse events & Field safety corrective actions to regulatory agencies while Maintaining Cochlear Implant Flow Data (IF) and Implant Traceability. · Perform Internal audit and issue audit reports, follow up on responses, CAPAs and close out internal audit. Interested candidates can share their resume on india.jobs@medel.com Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Schedule: Day shift Monday to Friday Ability to commute/relocate: Nehru Place, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: regulatory affairs: 1 year (Required) Language: English (Required) Work Location: In person

Junior Associate-Regulatory Affairs

Nehru Place, Delhi, Delhi

0 - 1 years

INR Not disclosed

On-site

Full Time

Opening with reputed MNC Medical Device Company for regulatory affairs domain. Position: Junior Associate- Regulatory Affairs Qualification: B.Pharmacy Location: Delhi NCR Job Profile: · Good Knowledge of Microsoft Excel and Microsoft office for maintaining import database and shipping documentation. · Supporting the Sales Teams on tender related issues/Documentation. · Support Import & logistics team and regulatory team in various work assigned · Manage, plan & execute labelling approvals of medical devices and accessories including labelling monitoring as per BIS and Legal Metrology and any other regulatory compliances that may become mandatory or statutory in the future. · Preparation, Scrutiny of documents, compilation, submission, follow ups for registration/ re-registration/ renewal applications · Maintain PMS Data and ensure timely reporting of adverse events & Field safety corrective actions to regulatory agencies while Maintaining Cochlear Implant Flow Data (IF) and Implant Traceability. · Perform Internal audit and issue audit reports, follow up on responses, CAPAs and close out internal audit. Interested candidates can share their resume on india.jobs@medel.com Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Schedule: Day shift Monday to Friday Ability to commute/relocate: Nehru Place, Delhi, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Required) Experience: regulatory affairs: 1 year (Required) Language: English (Required) Work Location: In person

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