Executive, Regulatory Affairs | Johnson & Johnson
- Executive, Regulatory Affairs | Johnson & Johnson Gurgaon
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Johnson & Johnson?
- FAQs
- Summary Table
Executive, Regulatory Affairs | Johnson & Johnson Gurgaon
Apply for Executive, Regulatory Affairs at Johnson & Johnson, Gurgaon. Life Sciences or Pharmacy graduates with regulatory experience preferred.
Johnson & Johnson (J&J), a global leader in healthcare innovation, is inviting applications for the position of Executive, Regulatory Affairs at its Gurgaon, Haryana location. This hybrid role offers an opportunity to work in one of the most respected healthcare companies in the world, ensuring compliance and excellence across J&J’s medical device and pharmaceutical portfolios.
This role is ideal for Life Sciences, Pharmacy, or Biomedical graduates who are passionate about regulatory affairs, product lifecycle management, and maintaining compliance with global and local health authorities.
Company Overview
Johnson & Johnson is one of the world’s most trusted healthcare companies, with a 130+ year legacy of innovation in MedTech and Pharmaceuticals. The company’s mission is to improve global health through scientific advancement, innovative products, and ethical leadership.
With a strong focus on regulatory excellence, quality assurance, and sustainable healthcare solutions, J&J plays a vital role in preventing, treating, and curing complex diseases worldwide.
In India, J&J operates multiple facilities supporting research, manufacturing, regulatory, and commercial functions, empowering professionals to shape the future of health for humanity.
Job Role & Responsibilities
As an Executive in Regulatory Affairs, you will be responsible for ensuring compliance with Indian and global medical device regulations while managing the product lifecycle for J&J’s medical franchises.
Key Responsibilities:
- Prepare, review, and submit regulatory filings including new registrations, re-registrations, and manufacturer transfers under the guidance of RA Leads or Supervisors.
- Draft and manage regulatory submissions, such as responses to queries, corrections, and post-registration notifications.
- Maintain Product Registration Request Forms (PRRF) and manage documentation for product changes, discontinuations, and approvals.
- Ensure regulatory database updates and documentation archival in internal systems.
- Collaborate with cross-functional teams to collect and compile submission documents within defined timelines.
- Support the development of regulatory strategies for new and existing products to ensure timely approvals.
- Assist in maintaining compliance with Medical Device Rules (MDR 2017) and global CE marking standards.
- Participate in regulatory audits, internal trainings, and cross-departmental meetings.
- Maintain and track key milestones and updates for franchise-related submissions in online business systems.
- Support the Regulatory Affairs Group in quality system compliance and documentation control.
Eligibility / Qualifications
Educational Background:
- Graduate or preferably Postgraduate in Life Sciences, Pharmacy, Biomedical Engineering, or related fields.
Experience:
- 1–3 years of experience in Regulatory Affairs, preferably within Medical Devices or Pharmaceuticals.
Core Competencies:
- Strong understanding of Medical Devices Rules, 2017 (India) and CE Marking requirements.
- Excellent oral and written communication skills for drafting regulatory responses.
- Proficiency in MS Word, Excel, and PowerPoint.
- Ability to coordinate effectively with internal and external stakeholders.
- Strong attention to detail, organizational, and documentation skills.
Preferred Skills:
- Familiarity with Regulatory Authority submissions, product lifecycle management tools, and change control procedures.
- Experience in handling post-market regulatory documentation and compliance audits.
Location & Salary
- Location: Gurgaon, Haryana, India
- Work Pattern: Hybrid (Office + Remote)
- Department: Regulatory Affairs Group
- Experience Level: Entry to Mid-Level (1–3 Years)
- Employment Type: Full-Time, Regular
- Compensation: Competitive salary with additional employee benefits and career advancement opportunities.
Application Process
Interested candidates can apply directly via Johnson & Johnson’s official careers portal. Ensure your resume highlights relevant regulatory experience, product lifecycle management exposure, and familiarity with Indian medical device regulations.
👉 Apply Here – Johnson & Johnson Careers Portal
⚠️ Apply before the closing date! Shortlisted candidates will be contacted for interviews and regulatory case discussions.
Why Join Johnson & Johnson?
- Be part of one of the most reputable healthcare organizations globally.
- Opportunity to work on end-to-end regulatory lifecycle management for innovative medical devices.
- Exposure to global regulatory frameworks (India MDR, CE Marking, USFDA, WHO).
- Inclusive, diverse, and innovation-driven culture that promotes continuous learning.
- Structured career development in Regulatory Affairs, Quality, and Compliance.
FAQs
Q1: Who can apply for the Executive, Regulatory Affairs role at Johnson & Johnson?
Graduates or postgraduates in Life Sciences, Pharmacy, or Biomedical fields with 1–3 years of regulatory experience.
Q2: What are the main responsibilities of this role?
To manage regulatory submissions, lifecycle updates, and compliance for medical device franchises in India.
Q3: Is prior experience in Medical Devices mandatory?
Preferred but not mandatory; candidates with pharma regulatory exposure may also apply.
Q4: What is the work model for this position?
The role follows a hybrid work pattern (office + remote flexibility).
Q5: What skills are required to succeed in this role?
Knowledge of MDR 2017, CE Marking, regulatory submission processes, and strong communication skills.
Q6: How do I apply?
Submit your application through the official Johnson & Johnson Careers Portal.
Summary Table
| Category | Details |
|---|---|
| Company | Johnson & Johnson |
| Vacancy | Executive, Regulatory Affairs |
| Required Education | Life Sciences, Pharmacy, Biomedical, Engineering |
| Experience | 1–3 Years |
| Location | Gurgaon, Haryana, India |
| Department | Regulatory Affairs Group |
| Work Pattern | Hybrid |
| Job Type | Full-Time, Regular |
| Apply Link | Apply Here |
To apply for this job please visit www.careers.jnj.com.
