Are you passionate about medical device regulations and looking to build a career in regulatory affairs? V-REG Solutions, a trusted name in regulatory consulting, is offering a Level I – Regulatory Intern position at its Ahmedabad office. This internship provides practical exposure to global regulatory frameworks (India, US FDA, EU) and offers mentorship from experienced professionals in the field.
This is an excellent opportunity for life sciences, pharmacy, and biomedical graduates who wish to enter the fast-growing medical device regulatory domain.
Internship Responsibilities
As a Regulatory Intern, you will:
- Assist in technical file preparation and regulatory submissions.
- Support quality management system (QMS) documentation under ISO 13485 standards.
- Conduct research on global medical device regulations.
- Prepare regulatory documentation, presentations, and reports.
- Collaborate with colleagues in a cooperative and uplifting work environment.
Qualifications
To be eligible, you should have:
- Degree in Life Sciences, Pharmacy, or Biomedical Sciences.
- Basic understanding of ISO 13485 medical device standard.
- Strong skills in MS Office (Excel, Word, PowerPoint).
- Good writing, documentation, and research skills.
- A strong interest in medical device regulatory affairs.
Benefits of the Internship
- Mentorship from senior regulatory professionals.
- Hands-on training in medical device regulatory submissions.
- Exposure to global regulatory frameworks (India, US FDA, EU).
- Practical knowledge of technical file preparation and QMS support.
- Duration: 6 months to 1 year.
- Location: Ahmedabad, Gujarat.
How to Apply
Interested candidates can send their updated CV to:
