Executive, Regulatory Affairs - Haryana, India - J&J Family of Companies

Description

Executive, Regulatory Affairs W

Description

Job title: Executive, Regulatory Affairs

Overall purpose of job:

• Regulatory compliance for the Medical Devices marketed by Johnson & Johnson MedTech India
• To maintain the Life cycle management of the product registered by Johnson & Johnson
• Coordinate with internal stakeholders to Developed regulatory strategies and mitigate interdependencies of overlapping projects to successfully submit application.

Essential duties and responsibilities:

• Draft, review and submission of Regulatory filings (Re-registrations/ New Registrations/ Legal-Physical manufacturer transfer) for India market.
• Draft, review and submission of other Regulatory submissions (Query responses, Corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for India market in accordance with applicable regulations and relevant guidelines.
• Draft cover letters for Regulatory communications/ submissions depending on level of regulatory knowledge/expertise.
• Update and live maintenance of business plan in sharepoint for assigned franchises/ licenses.
• Assist in the preparation of technical presentations/ meetings with regulator.
• Gathers and assembles information, prepares documents for New Product applications/Renewal Applications/Change Notifications/Response to Regulatory Agencies questions in accordance with regulations and relevant guidelines.
• Maintain the changes to the Regulations/Products/Sites and make necessary submission to maintain compliance to Country Regulations (Lifecycle management)
• Coordination with internal stakeholders ensuring compliant lifecycle management of responsible products/franchises.
• Maintain the changes to the Regulations/Products/Sites and make necessary submission to maintain compliance to Country Regulations
• Maintenance of RA database for the responsible franchises in MDRIM tool.
• Ensuring timely completion of received change assessment within due timeline and provide feedback to source RA team through email/other portals.
• Creation and maintenance of Product Registrations request Form (PRRF) for any registration activities under responsible franchises/ licenses and Change Controls for any product discontinuation/ changes as per defined procedure.
• Ensure on time archival of regulatory submission documents.
• Understand complaint & adverse event reporting responsibility and report such events within 24 hours of becoming aware.
• Other assignment identified and assigned by Supervisor/ management- time to time.

Special requirements:

• Knowledge of Medical Device Rule 2017 and Drugs and Cosmetics Act
• Knowledge in the international regulations of Medical Devices in US and EU
• Excellent proficiency with software tools

Job location:

Gurgaon, Haryana- India

Qualifications

Essential knowledge and skills:

• Graduate/ Post Graduate in Lifescience/ Bio Medical/ Pharmacy
• Minimum 2-4 years Industry Experience in Regulatory Affairs, preferably in medical devices. Sound understanding of MD rules and regulations in India.
• Experience of Submitting, Registering and maintaining Product registrations with MOH
• Experience in assembling product dossiers for submission to Regulatory Authorities.
• Good technical writing and communication skills.

Core competencies required for this role:

• Advanced computer skills specifically in MS Word, Excel, Internet Explorer, PowerPoint, and Outlook

Primary Location Asia Pacific-India-Haryana-Gurgaon

Organization Johnson & Johnson Private Limited (8080)

Job Function Regulatory Affairs

Req ID: W