Regulatory Medical Writer | Freshers & 0–2 Years | Remidio
- Remidio Hiring Regulatory Medical Writer | Freshers & 0–2 Years | Bangalore Life Sciences Jobs
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Skills Required:
- Experience:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What documents will I work on?
- Is regulatory knowledge required?
- What tools are required?
- What is the career growth?
Remidio Hiring Regulatory Medical Writer | Freshers & 0–2 Years | Bangalore Life Sciences Jobs
Remidio is hiring for the role of Regulatory Medical Writer in Bangalore. This is a high-impact opportunity for freshers and early-career professionals (0–2 years experience) to work at the intersection of clinical research, medical writing, and regulatory affairs in a fast-growing AI-driven healthcare company.
The company is offering multiple openings for this role, making it ideal for candidates from life sciences and pharmacy backgrounds who want to build a career in regulatory writing, clinical documentation, and medical device compliance.
Company Overview
Remidio is a global innovator in AI-powered ophthalmic solutions, focused on early detection of diseases such as diabetic retinopathy, glaucoma, and age-related macular degeneration. The company has achieved major regulatory milestones including CDSCO approval in India and CE marking under EU-MDR, along with FDA registration for its devices.
With operations across 40+ countries and over 16 million patients screened, Remidio combines advanced artificial intelligence with clinical expertise to deliver accessible, high-quality preventive healthcare solutions.
Job Role & Responsibilities
As a Regulatory Medical Writer, you will be responsible for developing clinical and regulatory documents required for global submissions and compliance.
Key responsibilities include:
- Prepare and review Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), and Post-Market Surveillance (PMS) reports
- Collaborate with clinical, regulatory, and R&D teams to gather and analyze data
- Ensure regulatory documentation complies with CDSCO, EU-MDR, and global guidelines
- Conduct literature searches using databases such as PubMed and Cochrane
- Extract and synthesize clinical data for regulatory submissions
- Maintain documentation accuracy, completeness, and audit readiness
- Support regulatory inspections and audits
- Stay updated with evolving regulatory requirements and communicate updates to stakeholders
This role plays a key part in ensuring compliance, product approval, and global market access for innovative medical technologies.
Eligibility / Qualifications
Candidates must meet the following educational requirements:
B.Pharm, M.Pharm, Pharm.D, BSc Life Sciences, MSc Life Sciences, Biotechnology, Biochemistry, Biomedical Sciences
Skills Required:
- Strong understanding of regulatory writing and clinical documentation
- Knowledge of CDSCO, EU-MDR, and global regulatory frameworks
- Proficiency in literature search tools (PubMed, Cochrane)
- Excellent scientific writing and communication skills
- Strong attention to detail and document quality standards
- Ability to manage timelines and work in a fast-paced environment
Experience:
- 0 to 2 years of experience in regulatory writing, clinical research, or medical writing
Location & Salary
- Location: Bangalore
- Work Mode: Full-Time (Onsite)
- Salary: Competitive salary based on medical writing and regulatory domain standards
Application Process
Interested candidates can apply through the official Remidio careers portal:
Apply Here: https://remidio.keka.com/careers/jobdetails/125713
Early application is recommended due to high demand for regulatory medical writing roles.
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
Yes, freshers and candidates with up to 2 years of experience can apply.
What documents will I work on?
Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), and PMS reports.
Is regulatory knowledge required?
Basic understanding is expected; training and exposure will be provided.
What tools are required?
Literature databases like PubMed and Cochrane.
What is the career growth?
You can grow into Senior Medical Writer, Regulatory Specialist, or Clinical Affairs roles.
| Category | Details |
|---|---|
| Company | Remidio |
| Vacancies | Regulatory Medical Writer |
| Required Education | B.Pharm, M.Pharm, Pharm.D, BSc/MSc Life Sciences, Biotechnology, Biochemistry |
| Experience | 0–2 Years |
To apply for this job please visit remidio.keka.com.
