Regulatory Affairs Jobs in India: Johnson & Johnson is Hiring an Executive | Apply Now
Looking to advance your career in Regulatory Affairs Jobs in India? Johnson & Johnson (J&J) offers an exciting opportunity for passionate Life Science professionals to join their Regulatory Affairs Group as an Executive, Regulatory Affairs in Gurgaon. This life science job lets you contribute to global healthcare innovation while ensuring regulatory compliance and product safety across J&J’s medical franchises in India.
Job Details:
- Job Title: Executive, Regulatory Affairs
- Category: Analyst, Regulatory Affairs (P4 – N23)
- Location: Gurgaon / India
- Requisition Number: R-042248
- Work Pattern: Hybrid Work
About the Company:
Johnson & Johnson (J&J) is one of the world’s most trusted and innovative healthcare companies, dedicated to improving health and well-being for people everywhere. With a legacy spanning over 135 years, J&J operates globally across pharmaceuticals, medical devices, and MedTech sectors, driving breakthrough innovations that advance healthcare for humanity.
In India, Johnson & Johnson continues to play a pivotal role in healthcare innovation, compliance, and quality assurance. The company fosters a culture of excellence, empowering Life Science professionals to contribute to high-impact projects in Regulatory Affairs, product development, and quality management.
J&J’s strong ethical foundation, commitment
to safety, and focus on scientific innovation make it an ideal workplace for those aspiring to build meaningful life science careers in a globally recognized organization.Education:
Graduate or preferably Postgraduate in Sciences/ Life Sciences.
Key responsibilities:
- Draft, review, submission and archival of Regulatory filings (Re-registrations/ New Registrations/ Legal-Physical manufacturer transfer) for India market under guidance and instructions of RA Leads/ Supervisor.
- Draft, review, submission and archival of Regulatory submissions (Query responses, Corrections filings, miscellaneous notifications regarding post registration regulatory lifecycle management) for India market in accordance with applicable regulations and relevant guidelines and instructions of RA leads/ Supervisor.
- 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.
- Update and live maintenance of business plan in online systems for assigned franchises/ licenses.
- Coordination with internal stakeholders through various modes (email/ phone/ document request tools) to ensure time bound availability of documents for regulatory application compilation and submissions.
- Attend applicable training sessions as well as complete mandatory on-line trainings and summit training records to the supervisor/ Admin assistant and work as per the applicable SOPs and guidelines.
- Coordination with internal stakeholders ensuring compliant lifecycle management of responsible products/ franchises.
- Maintenance of RA database for the responsible franchises in Internal tool.
- Other assignment identified and assigned by management- time to time.
Skills:
- Basic understanding of Medical Devices Rules, 2017 (India) and CE Marking of Medical Devices
- Good Oral & written communication. Efficient in creating draft letters and preparing response to India HA.
- Good hands-on experience in MS-Word, Excel and Power Point Presentation.
This is an excellent opportunity for Life Science graduates seeking to build a strong career in Regulatory Affairs Jobs in India. At Johnson & Johnson, you’ll play a vital role in ensuring product compliance and quality, supporting the company’s mission to advance health for humanity. Join a team that values innovation, collaboration, and regulatory excellence.
