Remidio Hiring Regulatory Analyst Clinical Affairs Job in Bangalore. Apply for medical device regulatory writing role with global healthcare innovation exposure.
Introduction
Remidio, a rapidly growing health-tech innovator in ophthalmology, is hiring a Regulatory Analyst – Clinical Affairs in Bangalore. This opportunity is ideal for professionals with 2–3 years of experience in regulatory medical writing, especially those working with medical devices or clinical documentation. If you are passionate about regulatory science and want to contribute to cutting-edge AI-powered healthcare technologies, this role offers strong growth potential in a globally expanding organization.
Candidates with expertise in CDSCO, EU MDR documentation, and clinical evaluation writing will find this role highly relevant and career-enhancing. Remidio Hiring Regulatory Analyst Clinical Affairs Job
Company Overview
Remidio is an emerging global leader in AI-driven ophthalmic technology, focused on improving early detection and preventive eye care worldwide. The company develops advanced diagnostic equipment powered by artificial intelligence, enabling faster and more accurate identification of vision-threatening diseases. With regulatory approvals across major global markets and deployment in multiple countries, Remidio continues to expand its footprint in digital healthcare innovation. The company’s mission revolves around making high-quality screening accessible and affordable, especially in underserved regions. Remidio Hiring Regulatory Analyst Clinical Affairs Job
Job Location & Employment Type
- Location: Bangalore / Bengaluru, India
- Employment Type: Full-Time
- Experience Level: 2–3 Years
- Department: Clinical Affairs / Regulatory
Open Position Details
Job Title: Regulatory Analyst – Clinical Affairs
Industry: Medical Devices / Digital Health
Function: Regulatory Medical Writing & Clinical Documentation
This role involves preparing clinical regulatory documentation and supporting global regulatory submissions for innovative ophthalmic devices. Remidio Hiring Regulatory Analyst Clinical Affairs Job
Key Roles & Responsibilities
The Regulatory Analyst will support clinical and regulatory teams in preparing high-quality documentation aligned with global standards. Key responsibilities include: Remidio Hiring Regulatory Analyst Clinical Affairs Job
- Preparing regulatory medical writing documents for device approvals and lifecycle management.
- Developing Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER).
- Drafting Post-Market Surveillance (PMS) reports and related compliance documents.
- Collaborating with cross-functional departments such as clinical, regulatory, and R&D teams.
- Performing detailed literature searches to support regulatory documentation.
- Extracting and synthesizing clinical evidence from peer-reviewed journals and databases.
- Ensuring all regulatory documents meet compliance requirements of CDSCO, EU MDR, and other global frameworks.
- Reviewing and editing technical content for clarity, accuracy, and scientific integrity.
- Supporting regulatory audits and inspections when required.
- Monitoring updates in regulatory guidelines and implementing necessary documentation changes.
- Maintaining document version control and regulatory compliance standards.
- Communicating regulatory implications of changes to internal stakeholders.
Eligibility Criteria
Education
- Bachelor’s degree in Life Sciences, Pharmacy, Biomedical Sciences, or a related discipline.
- Master’s degree or advanced qualification preferred but not mandatory.
Experience
- 2–3 years of experience in:
- Regulatory medical writing
- Clinical documentation for medical devices
- Pharma, biotech, or digital health sectors
Skills Required
- Hands-on experience with regulatory documentation such as CEP, CER, and PMS reports.
- Familiarity with global regulatory frameworks like CDSCO and EU MDR.
- Strong literature review skills using databases like PubMed or Cochrane Library.
- Ability to interpret and summarize clinical research effectively.
- Excellent scientific writing and editing skills.
- Strong organizational and documentation management abilities.
- High attention to detail and compliance-driven mindset.
- Ability to handle deadlines in a fast-paced regulatory environment.
- Strong interpersonal and cross-functional collaboration skills.
- Capability to work independently with minimal supervision.
Remidio Hiring Regulatory Analyst Clinical Affairs Job
Salary & Benefits
- Compensation will be as per company norms and aligned with industry standards.
- Additional benefits may include performance incentives, healthcare coverage, and opportunities for professional growth in a high-impact health-tech environment.
Selection Process
The hiring process may include the following stages:
- Application screening and shortlisting
- HR discussion
- Technical interview (regulatory/medical writing assessment)
- Final managerial interview
Only shortlisted candidates will be contacted for further evaluation.
How to Apply
Interested candidates should apply through the official Remidio careers portal or verified job listing platforms. Ensure your resume highlights regulatory documentation experience, especially related to medical devices and clinical evaluations.
Applicants are encouraged to submit updated CVs emphasizing regulatory writing samples, if available. Remidio Hiring Regulatory Analyst Clinical Affairs Job
Important Dates
- Application timeline has not been explicitly specified.
- Candidates are advised to apply at the earliest to avoid missing the opportunity.
Why Apply for This Pharma Job?
This position offers a unique chance to work at the intersection of AI, healthcare, and regulatory science. Here’s why this opportunity stands out:
- Work with a fast-growing global medical device innovator.
- Exposure to international regulatory standards like EU MDR.
- Opportunity to contribute to AI-based healthcare solutions.
- Strong learning curve in clinical regulatory documentation.
- High-impact role influencing patient screening worldwide.
- Career progression into senior regulatory or clinical affairs roles.
For professionals aiming to transition into medical device regulatory careers, this role provides excellent domain exposure and skill enhancement. Remidio Hiring Regulatory Analyst Clinical Affairs Job
Important Note
IndiaPharmaJobs.in is an independent platform that shares pharma, biotech, and healthcare job updates for informational purposes only. We are not affiliated with Remidio or any hiring organization mentioned. Candidates should always verify job details and apply through official company channels. Remidio Hiring Regulatory Analyst Clinical Affairs Job
Final Words
If you are looking to build a long-term career in regulatory affairs within the medical device or digital health sector, this Remidio opportunity is worth exploring. With a strong focus on innovation and global expansion, the company offers an exciting platform for regulatory professionals eager to make a meaningful impact. Apply early to improve your chances of securing this role. Remidio Hiring Regulatory Analyst Clinical Affairs Job
