V-REG Solutions is a specialized consulting firm focused on medical device and pharmaceutical regulatory compliance. Our team of experienced regulatory professionals provides end-to-end solutions, helping manufacturers navigate the complex landscape of global regulatory frameworks, including India CDSCO, US FDA, and EU MDR/IVDR.
Job Description: Level I Regulatory Intern
This internship is a unique chance to immerse yourself in the real-world applications of medical device regulations. You will work directly with senior consultants on live projects, gaining insights that are invaluable for your future career in regulatory affairs.
Key Responsibilities:
- Assist in the preparation and compilation of Technical Files and design dossiers for submissions.
- Support licensing and registration activities for various global markets.
- Conduct research on evolving medical device regulations in India, the US, and the EU.
- Provide essential support for maintaining Quality Management Systems (QMS) based on ISO 13485 standards.
- Aid in creating and reviewing standard operating procedures (SOPs) and other quality documentation.
- Collaborate with the team on regulatory strategies for new product launches.
Who We Are Looking For (Requirements)
The ideal candidate for this regulatory internship will possess:
- An educational background in Life Sciences, Biomedical Engineering, Pharmacy, or a related field.
- A basic understanding of the ISO 13485 Standard and quality systems.
- Proficiency in MS Office applications (Excel, PowerPoint, Word) is essential.
- Demonstrated good writing, research, and documentation skills.
- A strong interest in medical device regulations and a desire to build a career in this field.
- A cooperative, team-player attitude who enjoys working with colleagues in a cooperative and uplifting way.
Perks and Benefits of This Internship
This is more than just an internship; it’s a launchpad for your career. Here’s what you will gain:
- Expert Mentorship: Receive one-on-one guidance from experienced regulatory professionals with decades of industry knowledge.
- Exposure to Global Frameworks: Get direct exposure to global regulatory frameworks, including the US FDA, EU MDR, and India’s regulations.
- Practical, Resume-Boosting Skills: Develop practical skills in critical areas like Technical File preparation, licensing, and QMS support. This hands-on experience is highly valued by employers.
- Insightful Learning: Understand the end-to-end process of bringing a medical device to market compliantly.
How to Apply
If you are ready to take the first step towards a rewarding career in regulatory affairs, we want to hear from you!
To apply for this Regulatory Affairs Intern position, please send your updated CV or resume to info@vregsolutions.com.
