Regulatory Affairs Jobs: Join Johnson & Johnson Careers in Gurgaon
Looking for top Regulatory Affairs Jobs in the pharmaceutical industry? Johnson & Johnson Careers is hiring an Executive, Regulatory Affairs in Gurgaon, India. This hybrid role offers an exciting opportunity to contribute to regulatory compliance, product lifecycle management, and strategic submissions while advancing your Pharma Jobs career. Be part of a global leader in healthcare and drive impactful regulatory initiatives.
Job Details:
- Job Title: Executive, Regulatory Affairs
- Function: Regulatory Affairs Group
- Location: Gurgaon / India
- Requisition Number: R-042248
- Work Pattern: Hybrid Work
About the Company:
Johnson & Johnson Careers is a global leader in healthcare innovation, offering top Pharma Jobs that impact health worldwide. With expertise in Innovative Medicine and MedTech, J&J delivers solutions that prevent, treat, and cure complex diseases.
Job Description For Regulatory Affair Job
Johnson & Johnson Careers is offering a premier Regulatory Affairs Job in Gurgaon, ensuring regulatory and quality compliance across medical franchises in India. Responsibilities include lifecycle management of registered products, developing regulatory strategies, coordinating submissions with stakeholders, and ensuring alignment with regulatory agency requirements.
Key Responsibilities:
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Draft, review, submit, and archive regulatory filings for India (Re-registrations, New Registrations, Legal-Physical Manufacturer Transfers) – Regulatory Affairs Jobs.
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Prepare regulatory submissions including query responses, corrections, and miscellaneous post-registration filings.
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Create and maintain Product Registration Request Forms (PRRF) and Change Controls for product updates or discontinuation – Pharma Jobs.
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Maintain business plans for assigned franchises/licenses in online systems.
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Coordinate with internal stakeholders to ensure timely availability of documents for regulatory submissions.
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Attend mandatory trainings and maintain records as per SOPs and guidelines.
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Maintain RA databases for assigned franchises.
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Undertake other assignments as identified by management.
Qualifications: ideal for Regulatory Affairs Jobs
- Graduate or Postgraduate in Sciences, Life Sciences, Pharmacy, Biomedical, or Engineering.
- Basic understanding of Medical Devices Rules, 2017 (India) and CE Marking for Medical Devices.
- Strong oral and written communication skills, including drafting letters and preparing responses for India HA.
- Proficient in MS Word, Excel, and PowerPoint.
Preferred Skills:
- Hands-on experience with regulatory submissions and database management
- Ability to coordinate cross-functional projects and manage multiple timelines efficiently.
