RA Associate
Job Description:
Prepare and submit regulatory dossiers for product registrations, renewals, import licenses, and approvals.
Coordinate with regulatory authorities such as Central Drugs Standard Control Organization (CDSCO).
Manage regulatory compliance across India, Sri Lanka, Bangladesh, and Pakistan.
Support clinical trial application submissions, amendments, and approvals.
Obtain import/test licenses for clinical trial products.
Work closely with clinical, supply chain, and business teams.
Track approval timelines and maintain regulatory documentation.
Qualifications :
B.Pharm, M.Pharm, Biomedical Engineering, or Science degree.
Regulatory Affairs training preferred.
Minimum 1 year of experience in pharma, medical devices, or life sciences.
Knowledge of CDSCO applications and submission processes.
Key Skills :
Regulatory documentation and dossier preparation.
Product registration and license renewals.
Clinical trial regulatory submissions.
Strong communication and coordination skills.
Planning, organization, and reporting.
Time management and prioritization.
Independent and detail-oriented work style.
Additional Details :
1. Working Days: Monday to Friday
2. Experience: 1 Year
3. Gender Preference: Open to all
4. Working Hours: 9:00 AM to 5:00 PM
5. Interview Process: Virtual & Face to Face
6. Job Location: Delhi
7. Age Criteria: Up to 35 years
Contract period, auto-renewable or not: 1 year. Can be renewed with evaluation.
On Third Party Payroll (Talisman HR)
Interested can share updated cv to Saloni Pimenta on search@talismanstaffing.com or What's app : 9136435341
Company Profile
---rengthening our --- device leadership with innovations in cardiovascular and neuromodulation
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.