If you’re looking to start or grow your career in regulatory writing, this opportunity at Remidio could be a strong step forward. Known for its innovation in AI-powered eye care, Remidio is hiring a Regulatory Medical Writer in Bangalore. This role is ideal for candidates with 0–2 years of experience who want to work at the intersection of healthcare, technology, and regulatory science.
About the Company
Remidio is a global leader in AI-driven ophthalmic solutions, focused on early disease detection and accessible healthcare. The company has achieved significant milestones such as CDSCO approval for adaptive AI and CE marking under EU MDR. With FDA-registered devices and presence in 40+ countries, Remidio continues to transform preventive healthcare worldwide.
Job Details
Job Title: Regulatory Medical Writer
Location: Bangalore
Experience: 0–2 years
Job Type: Full-Time
Roles and Responsibilities
As a Regulatory Medical Writer, you will:
- Collaborate with cross-functional teams to collect and analyze clinical data
- Prepare regulatory documents such as:
- Clinical Evaluation Plans (CEP)
- Clinical Evaluation Reports (CER)
- Post-Market Surveillance (PMS) Reports
- Ensure all documents comply with CDSCO, EU MDR, and other regulatory standards
- Conduct literature reviews using platforms like PubMed and Cochrane
- Support audits, inspections, and regulatory submissions
- Stay updated with evolving regulatory guidelines and communicate updates internally
Required Qualifications
- Bachelor’s degree in Life Sciences, Pharmacy, or related field (Master’s preferred)
- 0–4 years of experience in regulatory medical writing (freshers can apply)
- Familiarity with CDSCO and EU MDR guidelines is an advantage
- Strong literature search and data interpretation skills
- Excellent written and verbal communication skills
- High attention to detail and ability to manage deadlines
Salary and Benefits
- Estimated Salary: ₹3.5 LPA – ₹7 LPA (depending on experience and skills)
- Opportunity to work with cutting-edge AI healthcare technology
- Exposure to global regulatory standards
- Career growth in medical writing and regulatory affairs
- Collaborative and innovation-driven work culture
