Bengaluru Karnataka Medical devices regulatory Jobs – 215 Open Jobs Today

Regulatory Medical Writer
Remidio —Bengaluru, Karnataka
- Bachelor's degree
- Communication skills
- Time management
Medical Writing Specialist
Zimmer Biomet —Bengaluru, Karnataka
- Full-time
- Writing skills
- English
- 12th Pass
Regulatory Affairs Specialist
Masimo —Bengaluru, Karnataka
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Access
Business Development Executive (BDE)
Konnectbrands —Bangalore City, Bengaluru, Karnataka
- ₹30,000.00 - ₹45,033.34 a month
- Full-time
- B.Sc
- Master's degree
- Bachelor's degree
Quick apply
Regulatory Affairs Expert
Fresenius Medical Care —Bengaluru, Karnataka
- Full-time
- Engineering
- English
- Master's degree
Sr Regulatory Operation Specialist
Philips —Bengaluru, Karnataka
- Full-time
- Microsoft Excel
- Engineering
- Microsoft Office
Staff Regulatory Affairs - Bangalore
Beckman Coulter Life Sciences —Bengaluru, Karnataka
- Full-time
- Remote
- Master's degree
- Project management
- AI
- Paid time off
- Work from home
Clinical Application Specialist – MR (Integration & Verification)
Philips —Bengaluru, Karnataka
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
10d
Quality Regulatory Operations Specialist
Masimo —Bengaluru, Karnataka
- Full-time
- Bachelor's degree
- Organisational skills
- Communication skills
Clinical Research Scientist
Niramai —Bengaluru, Karnataka
- Full-time
- Master's degree
- Bachelor's degree
- Computer networking
QARA Executive
Oivi —Bengaluru, Karnataka
- Hybrid work
- Engineering
- Microsoft Office
- Bachelor's degree
Senior Healthcare Research & Data Analyst - Spanish Language Expert
Clarivate —Bengaluru Urban District, Karnataka
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Word
- Spanish
Clinical Research Associate II
Fortrea —Bengaluru, Karnataka
- Full-time
- Patient monitoring
- Customer service
- Computer literacy
Lab Technician
SIGTUPLE TECHNOLOGIES PRIVATE LIMITED —Bengaluru, Karnataka
- ₹20,000 - ₹25,000 a month
- Full-time
- Microsoft Excel
- B.Sc
- Laboratory experience
- Health insurance
Quick apply
CRAII
Emmes Group —Bengaluru, Karnataka
- Full-time
- Remote
- Microsoft Office
- Bachelor's degree
- Organisational skills
Medical Writing Sr Specialist
Zimmer Biomet —Bengaluru, Karnataka
- Full-time
- Writing skills
- English
- 12th Pass
Mgr, Regulatory Affairs
Baxter —Bengaluru, Karnataka
- Doctoral degree
- English
- Master's degree
3h
Lead Medical Writer
Healthminds Consulting —Bengaluru, Karnataka
- Full-time
- Medicine
- Doctoral degree
- Master's degree
Regulatory Analyst - Clinical Affairs
Remidio —Bengaluru, Karnataka
- Bachelor's degree
- Communication skills
- Time management
Senior Regulatory Affairs
Saraca Solutions —Bengaluru, Karnataka
- Bachelor's degree
- Travel
- Communication skills

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Regulatory Medical Writer

Remidio
Bengaluru, Karnataka

Apply Now

Job details

Qualifications

Search engines
Diagnostic evaluation
Bachelor's degree
Communication skills
Time management

Full job description

About the Company:

Remidio is a global pioneer in AI-driven eye care, transforming healthcare with innovative ophthalmic equipment. As India’s first to secure CDSCO approval for adaptive ophthalmic AI and CE marking under EU-MDR, we lead early detection of diseases like diabetic retinopathy, glaucoma, and AMD, with ambitions to address systemic conditions like CVD and CKD. Our FDA-registered devices have screened over 16 million patients across 40+ countries, delivering fast, precise diagnoses. Founded 15 years ago with a vision to democratize preventive care, Remidio combines innovation and empathy to make quality healthcare accessible worldwide.

Position Overview:

We are seeking a highly motivated and detail-oriented Regulatory Medical Writer to join our team. The ideal candidate will have experience in creating clinical regulatory documents for the Central Drugs Standard Control Organization (CDSCO), the EU Medical Device Regulation (MDR), and other regulatory bodies. The Regulatory Medical Writer will play a crucial role in developing key documents such as Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), Post-Market Surveillance (PMS) Reports, and other regulatory submissions.

Responsibilities:

- Collaborate with cross-functional teams to gather and analyze clinical data for inclusion in regulatory submissions.
- Develop and maintain expertise in CDSCO, EU MDR regulations, and other regulatory guidelines, and standards related to clinical evaluations and post-market surveillance.
- Draft, review, and edit Clinical Evaluation Plans (CEP), Clinical Evaluation Reports (CER), Post-Market Surveillance (PMS) Reports, and other regulatory documents as required.
- Ensure accuracy, completeness, and compliance of regulatory documents with applicable regulations and guidelines.
- Provide support during regulatory inspections and audits, as needed.
- Stay informed about changes in regulatory requirements and guidelines and communicate implications to relevant stakeholders.

Qualifications:

- Bachelor's degree in a relevant scientific or technical discipline. An advanced degree is preferred.
- At least 0-4 years of experience in regulatory medical writing within the pharmaceutical, biotechnology, or medical device industry.
- Should be proficient in literature search engines like PubMed, Cochrane, etc., and capable of extracting relevant clinical studies for documentation.
- Experience with creating clinical regulatory documents for CDSCO and EU MDR is preferred.
- Strong understanding of regulatory requirements and guidelines governing clinical evaluations and post-market surveillance.
- Excellent written and verbal communication skills, with the ability to convey complex scientific information clearly and effectively.
- Detail-oriented with strong organizational and time management skills.
- Ability to work independently and collaboratively in a fast-paced, deadline-driven environment.

Apply Now

Refine Your Search

medical devices regulatory jobs in bengaluru karnataka

Regulatory Medical Writer

Medical Writing Specialist

Regulatory Affairs Specialist

Business Development Executive (BDE)

Regulatory Affairs Expert

Sr Regulatory Operation Specialist

Staff Regulatory Affairs - Bangalore

Clinical Application Specialist – MR (Integration & Verification)

Quality Regulatory Operations Specialist

Clinical Research Scientist

QARA Executive

Senior Healthcare Research & Data Analyst - Spanish Language Expert

Clinical Research Associate II

Lab Technician

CRAII

Medical Writing Sr Specialist

Mgr, Regulatory Affairs

Lead Medical Writer

Regulatory Analyst - Clinical Affairs

Senior Regulatory Affairs

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