The demand for skilled Medical Device Quality Assurance professionals is rising rapidly as companies strengthen regulatory and QMS compliance. V REG Solutions, a trusted name in regulatory and quality consulting, is now hiring a Quality Executive (Medical Devices) in Ahmedabad. This full-time role is ideal for candidates with 1–2 years of hands-on ISO 13485 experience who are ready to grow in a dynamic consulting environment.
If you are committed to quality, regulatory compliance, and continuous improvement, this opportunity is designed for you.
🔍 Key Responsibilities
As a Quality Executive, you will play a key role in supporting quality systems and regulatory activities:
- Support the implementation and maintenance of ISO 13485:2016 Quality Management System
- Conduct internal audits, documentation review, and manage CAPA activities
- Assist in regulatory submissions, compliance checks, and documentation updates
- Coordinate with clients and internal stakeholders for QMS enhancements
- Travel to client sites for audits, inspections, and QMS support as required
🎓 Required Skills & Qualifications
- Bachelor’s degree in Engineering / Life Sciences / Biomedical / related field
- 1–2 years of experience in Medical Device Quality Assurance
- Good understanding of ISO 13485, EU MDR (preferred), QMS documentation
- Strong communication, analytical thinking, and documentation skills
- Ability to work with cross-functional teams and manage client interactions
🌟 Why Join V REG Solutions?
- Work with leading experts in the medical device regulatory and QMS consulting domain
- Exposure to real-world client audits and compliance improvement projects
- Opportunity to grow into senior quality or regulatory roles
- Professional, supportive, and high-learning environment
📩 How to Apply
Interested and eligible candidates can apply immediately.
👉 Send your CV to: info@vregsolutions.com
🔒 Only candidates with relevant experience will be considered. Freshers should not apply.
