V-REG Solutions is a leading regulatory consulting firm specializing in medical device compliance and quality management systems. With a strong focus on innovation and regulatory excellence, V-REG supports clients worldwide in navigating complex regulatory landscapes. The company is committed to nurturing young talent through mentorship and practical training.
Job Description: Level I Regulatory Intern
As a Level I Regulatory Intern at V-REG Solutions, you will:
- Assist in the preparation of Technical Files and regulatory submissions.
- Support Quality Management System (QMS) documentation and compliance activities.
- Conduct research on medical device regulations and standards.
- Collaborate with experienced regulatory professionals to understand global regulatory requirements.
- Gain exposure to ISO 13485 standards and regulatory frameworks such as India’s CDSCO, US FDA, and EU MDR.
- Develop strong writing, documentation, and presentation skills using MS Office tools.
Requirements
- Educational background in Life Sciences, Biomedical Engineering, Pharmacy, or related fields.
- Basic understanding of ISO 13485 standard.
- Proficiency in MS Office (Excel, PowerPoint, Word).
- Strong writing, research, and documentation skills.
- Keen interest in medical device regulations.
- Ability to work cooperatively and maintain a positive team environment.
Perks of This Internship
- Mentorship from experienced regulatory professionals.
- Hands-on experience with global regulatory frameworks.
- Practical skills in Technical File preparation, licensing, and QMS support.
- Opportunity to build a strong foundation in medical device regulatory affairs.
How to Apply
Interested candidates are invited to send their updated CV to info@vregsolutions.com. For more information about V-REG Solutions and their services, visit their official website: www.vregsolutions.com.
