Johnson & Johnson (J&J), a global leader in healthcare innovation, is inviting applications for Executive and Senior Executive – Regulatory Affairs positions in Mumbai, India.
These roles are ideal for life science professionals passionate about regulatory compliance, product registration, and lifecycle management within the pharmaceutical and medtech sectors.
If you’re detail-oriented and eager to grow your career with one of the world’s most trusted healthcare companies, this is your chance.
About Johnson & Johnson
At Johnson & Johnson, innovation meets purpose. With a mission to build a world where complex diseases are prevented, treated, and cured, J&J continues to drive breakthroughs in Innovative Medicine and MedTech to profoundly impact health for humanity.
Learn more: https://www.jnj.com
Open Positions
1. Executive – Regulatory Affairs (Hybrid, Mumbai)
Key Responsibilities:
- Maintain and update regulatory trackers and submission records for India.
- Prepare complete dossiers, query responses, and support product registrations across multiple therapeutic portfolios.
- Coordinate with global teams to arrange finished product (FP) samples and reference standards for testing at government labs.
- Manage lifecycle activities like RC and IL renewals to ensure business continuity.
- Archive approvals, query letters, and maintain SEC meeting minutes.
- Support QMS documentation and assist team members in operational tasks.
Preferred Skills:
Regulatory compliance, dossier preparation, quality assurance (QA), project management, analytical reasoning, process-oriented mindset.
2. Senior Executive – Regulatory Affairs (Onsite, Mumbai)
Key Responsibilities:
- Ensure timely registration submissions, renewals, and CMC variations.
- Draft and compile regulatory documentation and artwork manuscripts.
- Liaise with global and local teams for testing and compliance activities.
- Maintain adherence to internal and external regulatory standards.
- Collaborate cross-functionally with medical and supply chain teams.
- Support packaging material specification and artwork development.
Preferred Skills:
Regulatory development, product licensing, clinical trial assistance, medicines and device regulation, risk assessments, communication, and teamwork.
Who Can Apply
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Chemistry, or Biotechnology.
- 2–6 years of experience in Regulatory Affairs or Pharmaceutical Compliance.
- Strong understanding of product registration processes, dossier compilation, and global regulatory standards.
Benefits
- Competitive salary package (₹6–12 LPA depending on experience).
- Hybrid or onsite flexibility (role-dependent).
- Global collaboration and exposure to innovative healthcare projects.
- Career development and training in regulatory leadership.
Application Details
📍 Location: Mumbai, India
Application Link for Executive – Regulatory Affairs (Hybrid, Mumbai)
Application Link for Senior Executive – Regulatory Affairs (Onsite, Mumbai)
