Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
Post: Sr. Executive Regulatory Affairs
Job Description
J&J Medical India (JJMI) is the market leader in the Medical Company Devices Industry in India. It is in the business of caring and providing solutions to doctors, patients and nurses. It comprises of multiple Franchises (Strategic business units) providing healthcare solutions across Vision Care, Orthopaedics, Infection Prevention, Wound Management, Women’s health, minimally invasive surgery, Circulatory disease management, and Blood glucose monitoring and insulin delivery.
Responsibilities
• Draft, review and submission of Regulatory filings (Re-registrations/ New Registrations/ Legal-Physical manufacturer transfer) for India, under guidance and instructions of Supervisor.
• Draft, review and submission of other Regulatory submissions (Query responses, Corrections fillings, miscellaneous notifications regarding post registration regulatory lifecycle management) for India in accordance with applicable regulations and relevant guidelines, under guidance and instructions of Supervisor.
• Draft cover letters for Regulatory communications/ submissions depending on level of regulatory knowledge/expertise.
• Gathers and assembles information/ technical & regulatory documents through various modes (email/ document request tools/ T-cons) in timely manner ensuring regulatory application submissions as per defined plan/ commitment.
• Coordination with internal stakeholders ensuring compliant lifecycle management of responsible products/ franchises.
• Maintain the changes to the Regulations/Products/Sites and make necessary submission, as assigned, to maintain compliance to Country Regulations
• Attend applicable training sessions as well as complete mandatory on-line e University trainings and submit training records to the supervisor / Admin assistant and work as per the applicable SOPs and guidelines
• Maintenance of RA database for the responsible franchises in Trackwise tool (PRIM) & MDRIM.
• Ensuring timely completion of received change assessment within due timeline and provide feedback to source RA/ RALI team through email/ trackwise.
• Control of regulated/ non-regulated products/ codes in RA gateway tool.
• Coordinate with source RA and other stakeholders for tender related regulatory support and responsible for update and maintenance of Tender related sharepoint.
• Other assignment identified and assigned by Supervisor/ management- time to time.
Candidate Profile
1) Graduate/ Post Graduate in Lifescience/ Bio Medical/ Pharmacy
2) Minimum 1-3 years Industry Experience in Regulatory Affairs, preferably in medical devices and Biologicals.
Skill and Behavioral
• Sound understanding of MD&D rules and regulations in India.
• Experience of Submitting, Registering and maintaining Product registrations with MOH
• Experience in quality/ manufacturing and regulatory affairs in medical devices would be advantage
• Experience in assembling product dossiers for submission to Regulatory Authorities.
• Good technical writing, communication skills and negotiation skills.
Additional Information
Experience: 1-3 years
Qualification: Post Graduate- LifeScience/ Bio Medical/ Pharmacy
Location: Haryana-Gurgaon
Functional Area: Regulatory Affairs
Industry Type: Pharma/Biotech/Clinical Research
End Date: 20th March, 2018
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