A reputed pharmaceutical organization is inviting applications for the Regulatory Affairs Department for the positions of Executive and Senior Executive. This is an excellent opportunity for candidates with experience in regulatory documentation and API submissions to advance their careers in the pharma industry.
If you have hands-on experience in post-approval changes and Module 3 documentation, this role can be a strong step forward.
Job Details
Open Positions
- Executive
- Senior Executive
Department
Regulatory Affairs
Experience Required
- 3 to 6 Years
Qualification
- MSc in Chemistry
Roles and Responsibilities
As part of the Regulatory Affairs team, selected candidates will be responsible for:
- Handling regulatory documentation related to post-approval changes
- Preparing and reviewing Module 3 (Quality) sections for API submissions
- Ensuring compliance with global regulatory requirements
- Coordinating with cross-functional teams for submission data
- Supporting dossier compilation and lifecycle management activities
- Maintaining accurate records and regulatory databases
Required Skills
- Strong understanding of regulatory guidelines
- Experience in drafting and reviewing Module 3 documents
- Knowledge of API regulatory submissions
- Attention to detail and documentation accuracy
- Good communication and coordination skills
Salary and Benefits
- Estimated Salary Range: โน4,00,000 โ โน8,00,000 per annum
- Competitive compensation based on experience
- Opportunity to work in a reputed pharma environment
- Career growth in Regulatory Affairs domain
- Exposure to global regulatory standards
How to Apply
Interested candidates can apply through the official application process using the QR code provided in the job post or by visiting the companyโs career portal.
Make sure your resume highlights your experience in regulatory documentation and Module 3 submissions.
