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Synthimed is a pharmaceutical research and regulatory support organization working with global regulatory frameworks such as ICH, WHO, and CDSCO. The company specializes in documentation, regulatory submissions, data evaluation, and lifecycle management. Joining Synthimed gives fresh graduates direct learning exposure in real-world regulatory processes.
Job Role: Trainee – Drug Regulatory Affairs (DRA)
Key Responsibilities
- Assist in preparing regulatory documents, technical files, and product dossiers
- Support compilation and review of data for regulatory submissions
- Learn international & regional guidelines (ICH, WHO, CDSCO)
- Maintain accurate documentation and adhere to workflow systems
- Perform literature reviews and regulatory data checks
- Collaborate with the regulatory team for submissions and updates
Eligibility & Qualifications
- M.Sc in Organic Chemistry (primary requirement)
- M.Sc in Analytical/Pharmaceutical Chemistry or PG Diploma in DRA is also acceptable
- Strong concepts in organic chemistry, reaction mechanisms, and chemical analysis
- Good documentation & analytical skills
- Freshers and early-career candidates are eligible
Preferred Backgrounds
- MSc Organic Chemistry
- MSc Analytical Chemistry
- MSc Pharmaceutical Chemistry
- PG Diploma/Certificate in Drug Regulatory Affairs
- M.Pharm (Regulatory Affairs)
Job Location & Salary
- Locations: Chandigarh, Mohali, Derabassi
- Salary: ₹18,000 – ₹25,000 per month (typical industry range for trainee DRA roles)
Benefits of Joining Synthimed
- Structured learning and regulatory training
- Exposure to international guidelines (ICH, WHO, CDSCO)
- Opportunity for long-term career growth in regulatory affairs
- Hands-on experience in dossier preparation & compliance
- Professional mentorship from experienced regulatory teams
How to Apply
Send your updated resume to:
📧 Email: astha.trivedi@synthimed.com
📞 Contact: +91 89683 74200