Looking to build a career in clinical research, regulatory affairs, and medical device compliance? Meril, a leading medical device company in India, is hiring a Clinical Specialist in Vapi, Gujarat. This opportunity is ideal for candidates with a background in BDS, biotechnology, or life sciences who want hands-on exposure in clinical evaluation reports (CER), CDSCO submissions, and post-market surveillance (PMS).
This Clinical Specialist job in Gujarat offers a strong entry point into the growing medical device regulatory affairs sector, combining clinical data analysis, documentation, and compliance management.
Job Details
- Position: Clinical Specialist
- Company: Meril
- Location: Vapi, Gujarat
- Experience: 1โ2 Years
- Qualification: BDS / M.Sc / B.Tech (Life Sciences, Biotechnology, Biomedical Sciences)
Key Responsibilities
Clinical Evaluation & Research
- Assist in drafting and updating Clinical Evaluation Reports (CER)
- Conduct systematic literature reviews and analyze clinical evidence
- Document clinical safety and performance data across product lifecycle
Regulatory Affairs & Compliance
- Prepare and manage CDSCO submissions and regulatory dossiers
- Maintain technical files, clinical logs, and evaluation reports
- Ensure compliance with MDR (Medical Device Regulations)
Post-Market Surveillance (PMS)
- Monitor and document PMS data and clinical follow-ups
- Support ongoing clinical safety updates and reporting
Lab Coordination & Testing
- Coordinate with labs for biocompatibility testing
- Track and manage testing timelines and documentation
Required Qualifications
- Education: BDS / M.Sc / B.Tech in Life Sciences, Biotechnology, Biomedical Sciences
- Experience: 1โ2 years in medical devices, clinical research, or pharma industry
- Skills Required:
- Clinical research & medical writing expertise
- Knowledge of CDSCO guidelines and MDR regulations
- Strong analytical and documentation skills
- Excellent organizational and communication abilities
Salary & Benefits
- Estimated Salary: โน3.5 โ โน6 LPA (based on experience)
- Opportunity to work in regulatory affairs and clinical evaluation
- Exposure to global medical device compliance standards
- Career growth in clinical research and regulatory domain
Why This Role is High-Demand
The demand for Clinical Specialists in India is rapidly growing due to stricter medical device regulations and CDSCO compliance requirements. Professionals skilled in CER writing, PMS, and regulatory submissions are highly valued across pharma and medtech companies.
How to Apply
Interested candidates can apply by sending their updated resume:
- Email: siddhiram.pareek@merillife.com
- Subject Line: Application for Clinical Specialist โ [Your Name]