Johnson & Johnson hiring Executive – Regulatory Affairs & Packaging Development
- Johnson & Johnson hiring Executive – Regulatory Affairs & Packaging Development in Mumbai. Regulatory affairs professionals eligible. Hybrid role.
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience Requirement
- Required Skills
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this a freshers role?
- Is this role focused only on packaging?
- What health authority interactions are involved?
- Is the role hybrid or onsite?
- What is the career growth after this role?
- Job Summary Table
Johnson & Johnson hiring Executive – Regulatory Affairs & Packaging Development in Mumbai. Regulatory affairs professionals eligible. Hybrid role.
Johnson & Johnson is hiring an Executive – Regulatory Affairs and Packaging Development for its Regulatory Affairs Group in Mumbai, India. This role is suited for regulatory affairs professionals who want to work at the intersection of regulatory product submissions, lifecycle management, and packaging development within a global healthcare organization. The position offers exposure to drug registration activities, health authority submissions, and post-marketing regulatory compliance in a hybrid work environment.
Company Overview
Johnson & Johnson is one of the world’s most respected and diversified healthcare companies, operating across Innovative Medicine and MedTech. With a strong focus on science-driven innovation, ethical practices, and patient-centric healthcare solutions, the company plays a critical role in preventing, treating, and managing complex diseases globally.
In India, Johnson & Johnson maintains a strong presence across pharmaceuticals, medical devices, and regulatory operations. The organization is known for its robust regulatory systems, compliance-driven culture, and commitment to global health authority standards. Working with Johnson & Johnson adds significant professional credibility and long-term career value in regulatory affairs and healthcare compliance.
Job Role & Responsibilities
As an Executive – Regulatory Affairs and Packaging Development, you will support regulatory product submissions, registration activities, and lifecycle management of pharmaceutical products. The role requires close coordination with internal teams, regulatory consultants, and health authorities.
Key Responsibilities
- Compile and prepare regulatory documents required for drug registration submissions
- Coordinate with regional and global regulatory teams to obtain supporting documents and dossiers
- Support regulatory submissions related to post-marketing surveillance (PMS) and Phase IV studies
- Prepare and submit quarterly and six-monthly PMS study reports, clinical reports, stability protocols, and non-clinical study documentation
- Liaise with regulatory consultants to ensure effective application submissions to the Drug Controller General of India (DCGI)
- Manage archival of regulatory dossiers, approvals, and DCGI submission copies
- Provide regulatory support for lifecycle management of registered pharmaceutical products
- Maintain regulatory trackers and support tender activities by providing required regulatory documentation
This role directly contributes to regulatory compliance, timely product approvals, and continued market access for healthcare products.
Eligibility / Qualifications
Required Education
Candidates should possess a relevant qualification in one of the following:
Pharmacy, Pharmaceutical Sciences, Life Sciences, Regulatory Affairs, Packaging Technology
Experience Requirement
- Relevant experience in regulatory affairs, product submissions, or regulatory documentation
- Exposure to drug registration processes and health authority submissions is preferred
Required Skills
- Strong understanding of regulatory product submissions and registration processes
- Knowledge of Indian regulatory requirements and DCGI submissions
- Ability to manage regulatory documentation, trackers, and archives
- Strong analytical reasoning and attention to detail
- Effective business writing and communication skills
- Ability to collaborate with cross-functional and global teams
- Understanding of regulatory compliance, risk assessment, and lifecycle management
Location & Salary
- Job Location: Mumbai, India
- Work Pattern: Hybrid
- Function: Regulatory Affairs Group
- Employment Type: Full-time
Application Process
Interested candidates can view the job details and apply through the official Johnson & Johnson careers portal:
Apply Online: https://www.careers.jnj.com/en/jobs/r-049016/executive-regulatory-affairs-and-packaging-development/
Please note that the employer has indicated that a candidate may already be identified for this role.
Frequently Asked Questions (FAQs)
Is this a freshers role?
No. This role requires prior experience in regulatory affairs or regulatory documentation.
Is this role focused only on packaging?
No. The role covers regulatory affairs, product submissions, lifecycle management, and packaging development support.
What health authority interactions are involved?
The role involves coordination with regulatory consultants and submissions to DCGI.
Is the role hybrid or onsite?
This position follows a hybrid work model based in Mumbai.
What is the career growth after this role?
Career progression includes Senior Regulatory Affairs Executive, Regulatory Affairs Manager, and global regulatory roles.
Job Summary Table
| Company | Johnson & Johnson |
|---|---|
| Vacancies | Executive – Regulatory Affairs and Packaging Development |
| Required Education | Pharmacy, Pharmaceutical Sciences, Life Sciences, Regulatory Affairs, Packaging Technology |
| Experience | Experienced Professionals |
To apply for this job please visit www.careers.jnj.com.
