Johnson & Johnson was founded more than 120 years ago on a revolutionary idea: Doctors and nurses should use sterile sutures, dressings and bandages to treat peoples’ wounds. Johnson & Johnson is ranked by Fortune Magazine as the 3rd most Admired Pharmaceutical Company in the world with an outstanding product range as well as an extensive research base with a number of life saving original research molecules.
Janssen Cilag, the pharmaceutical business of Johnson & Johnson has a presence in high growth pharma markets like Oncology, Nephrology, CNS, Gastroentrology, Dermatology, Neurology, and Gynecology among others.
Post : Assistant Manager RA
Job Responsibility:
• 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.
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.
Candidate Profile
Graduate/ Post Graduate in Lifescience/ Bio Medical/ Pharmacy
Minimum 1-3 years Industry Experience in Regulatory Affairs, preferably in medical devices (Orthopedic Devices).
Additional Information:
Location: Haryana-Gurgaon
Education: Graduate/Post graduate in Lifescience/ Bio Medical/ Pharmacy
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: Regulatory Affairs
Job Code: 1705616590W
End Date: 20th January, 2018
See All J&J Alerts B.Pharm Alerts B.Sc Alerts M.Sc Alerts
See All Other Jobs in our Database.
.png)
