Medirise Pharma is hiring a Regulatory Affairs Executive in Mumbai Suburban, Maharashtra. This is a full-time, permanent opportunity for professionals with 1–3 years of experience in pharmaceutical regulatory affairs.
The selected candidate will support regulatory dossier preparation for ROW (Rest of World) markets, work in accordance with ICH guidelines, and collaborate with cross-functional teams on product lifecycle management.
Medirise Pharma Regulatory Affairs Executive – Job Highlights
| Details | Information |
|---|---|
| Company | Medirise Pharma / Sovvaka Global Private Limited |
| Position | Regulatory Affairs Executive |
| Department | Legal & Regulatory |
| Experience | 1–3 Years |
| Qualification | Any Graduate |
| Location | Mumbai Suburban, Maharashtra |
| Employment Type | Full Time, Permanent |
| Openings | 1 |
| Industry | Pharmaceutical & Life Sciences |
| Salary | Approximately ₹3.5–₹6.0 LPA* |
*The job listing does not disclose a salary. The range above is an estimated market range for this experience level and should not be treated as an official company salary.
Regulatory Affairs Executive Responsibilities
The Regulatory Affairs Executive will be responsible for supporting regulatory activities associated with pharmaceutical products and international markets.
Key responsibilities include:
- Preparing regulatory dossiers for ROW markets in compliance with applicable ICH guidelines.
- Supporting regulatory documentation and submission activities.
- Coordinating with cross-functional teams involved in product development and commercialization.
- Contributing to product lifecycle management activities.
- Reviewing regulatory requirements and ensuring documentation is aligned with applicable guidelines.
- Supporting timely completion of regulatory deliverables.
Regulatory Affairs Executive Qualification
Candidates interested in the Medirise Pharma Regulatory Affairs Executive vacancy should meet the following requirements:
- Education: Any Graduate.
- Experience: 1–3 years of relevant professional experience.
- Working knowledge of Regulatory Affairs.
- Experience or exposure to CTD dossier preparation.
- Understanding of ROW market regulatory requirements.
- Familiarity with ICH guidelines is advantageous.
- Good coordination and communication skills for working with cross-functional teams.
Key Skills
The job listing highlights the following skills:
- Regulatory Affairs
- CTD Dossier Preparation
- ROW Market Regulatory Requirements
- ICH Guidelines
- Product Lifecycle Management
- Cross-functional Coordination
- Regulatory Documentation
Why Consider This Regulatory Affairs Job in Mumbai?
This opportunity can be relevant for pharmaceutical professionals looking to strengthen their experience in international regulatory affairs, particularly ROW market submissions and CTD dossier preparation.
Working with cross-functional teams can also provide exposure to different stages of the pharmaceutical product lifecycle and regulatory compliance processes.
How to Apply for Medirise Pharma Recruitment?
Eligible candidates interested in the Regulatory Affairs Executive job in Mumbai should refer to the original recruitment listing and submit their application through the designated application process.
Job Location: Mumbai Suburban, Maharashtra
Experience Required: 1–3 Years
Employment: Full Time, Permanent
Openings: 1
Candidates should ensure that their CV highlights relevant experience in regulatory affairs, CTD dossier preparation, ROW markets, and ICH guidelines.
About Sovvaka Global Private Limited
According to the provided job information, Sovvaka Global Private Limited is a pharmaceutical company focused on delivering healthcare solutions and has operations spanning markets including Africa, Europe, and South America. The company connects pharmaceutical manufacturing capabilities in India with international markets.