Are you a science postgraduate looking to start your career in regulatory affairs, data management, compliance, or product information management? A leading organization is hiring an Intern – Regulatory Information Management in Mumbai, India. This opportunity is ideal for freshers with a Master’s degree in Chemistry, Biology, Environmental Sciences, Toxicology, or related scientific disciplines.
The internship provides hands-on exposure to Regulatory Information Management, SHEQ (Safety, Health, Environment & Quality), Operations, Logistics, and Marketing Data Management, making it an excellent entry point into the pharmaceutical, chemical, life sciences, and regulatory compliance industries.
Job Overview
| Details | Information |
|---|---|
| Position | Intern – Regulatory Information Management |
| Location | Mumbai, India |
| Job Type | Internship |
| Experience | Freshers Eligible |
| Qualification | Master’s Degree in Science |
| Application Deadline | 30 June 2026 |
| Shift | Fixed & Rotational Shifts (including night shifts) |
Key Responsibilities
Selected interns will receive training in one or more domains including SHEQ, Operations, and Marketing.
SHEQ (Safety, Health, Environment & Quality)
- Validate regulatory documentation and product information.
- Review GHS classifications and REACH compliance data.
- Support biocides and trade control regulatory activities.
- Verify pharmaceutical, food, cosmetics, and market-specific regulations.
- Maintain data quality and integrity across regulatory databases.
- Assist in improving Safety Data Sheet (SDS) and Technical Data Sheet (TDS) automation processes.
Operations
- Validate logistics and operational documentation.
- Review packaging and transportation compliance information.
- Verify dangerous goods classifications.
- Maintain shelf-life, storage, and warehouse-related product data.
- Ensure operational information remains accurate and up to date.
- Support process automation and data extraction improvements.
Marketing
- Validate product descriptions and application information.
- Upload and manage product-related documentation.
- Monitor document expiration and coordinate updates.
- Maintain customer portal information.
- Improve Technical Data Sheet and product catalog automation.
Required Qualifications
Candidates should possess:
- Master’s Degree in:
- Chemistry
- Biology
- Environmental Sciences
- Toxicology
- Related Scientific Disciplines
Preferred Skills
- Freshers are encouraged to apply.
- Strong attention to detail.
- Excellent project and time management skills.
- Customer-focused mindset.
- Strong English communication skills.
- Knowledge of French or Spanish is an added advantage.
- Advanced MS Excel proficiency.
- Ability to work in rotational and night shifts.
- Strong analytical and data validation capabilities.
Why Apply for This Regulatory Affairs Internship?
This internship offers exposure to several high-demand career pathways, including:
- Regulatory Affairs
- Regulatory Information Management
- Product Stewardship
- Pharmacovigilance Support Functions
- Quality & Compliance
- Data Management
- Supply Chain Compliance
- Product Information Management
Candidates gain practical experience with global regulations, compliance documentation, and data governance systems that are highly valued across pharmaceutical, chemical, and life sciences companies.
Career Growth Opportunities
After successful completion, candidates may pursue roles such as:
- Regulatory Affairs Associate
- Regulatory Information Specialist
- Compliance Analyst
- Product Stewardship Associate
- Quality Documentation Executive
- Safety Data Management Associate
- Scientific Data Analyst
How to Apply
