Are you an experienced medical writer looking to step into the fast-growing world of medical devices? Here’s your chance! A leading organisation in Pune is conducting a walk-in drive for a Medical Writer – Post Market Surveillance role. If you’re passionate about medical writing and want to contribute to life-changing innovations, this opportunity is for you.
🌟 About the Role
As a Medical Writer in Medical Devices, you’ll be responsible for crafting high-quality scientific and regulatory documentation that supports the safety, performance, and compliance of medical devices.
Your contributions will directly impact patient safety and the product’s lifecycle in global markets.
🌈 Key Responsibilities
- Medical Writing: Prepare accurate, clear, and compliant documentation such as Post-Market Surveillance (PMS) reports and technical documents.
- Regulatory Compliance: Ensure all written materials meet global regulatory standards and industry guidelines.
- Cross-Functional Collaboration: Work closely with engineering, regulatory, and quality teams to gather data and draft high-quality content.
📚 Requirements
- Education:
Graduate in Biomedical Engineering, Pharmacy, OR Post-Graduate in Life Sciences. - Experience:
2–8 years of experience in medical writing (device writing preferred). - Skills:
- Strong command of English
- Knowledge of medical device documentation
- Ability to work in rotational shifts
🌟 What You Can Expect
- Competitive Salary: Attractive package aligned with industry standards.
- Career Growth: Excellent opportunities to advance your expertise in medical devices.
- Dynamic Work Culture: Be part of an expert team committed to innovation, safety, and compliance.
📅 Walk-in Drive Details
- Date: November 20, 2025
- Time: 10:00 AM – 12:30 PM
- Location:
Unit 2, Plot No 31,
Hinjewadi Phase 2, Rajiv Gandhi Info Tech Park,
Pune, Maharashtra – 411057 - Contact Persons: Varsha / Riya
📝 Documents to Carry
- Updated CV/Resume
- Original Government ID Proof
📚 Tips to Succeed in the Walk-In
- Prepare Well: Understand PMS documentation and medical device regulations.
- Dress Smart: Project confidence and professionalism.
- Carry Extra Resume Copies: Always good to have backups.
🤔 Why Choose This Role?
- Work in a leading medical device organisation.
- Gain exposure to global regulatory frameworks.
- Be part of a skilled, collaborative, and innovative team shaping the future of medical devices.