Professional Overview
Meet Dudhatra is an ambitious graduate student actively seeking internship and co-op opportunities in the field of Regulatory Affairs. With a strong educational background in Regulatory Affairs of Drugs, Biologics, and Medical Devices, Meet is poised to leverage their knowledge and passion to make a meaningful impact in the pharmaceutical and medical technology industries.
Experience Summary
Current Role
As a graduate student at Northeastern University, Meet is currently pursuing an MS in Regulatory Affairs. In this capacity, they are developing a comprehensive understanding of regulatory frameworks, guidelines, and best practices governing the development, approval, and post-market surveillance of pharmaceutical and medical products.
Career Progression
Meet's previous internship experiences have provided them with valuable hands-on exposure to the regulatory affairs function. As a Regulatory Affairs Intern at Sen-Jam Pharmaceutical, they gained insights into the submission and approval processes for new drug applications. Prior to that, Meet served as a Quality Assurance Operational Intern at Dolphin Pharmaceutical Ltd. and a Regulatory Affairs Intern at Globela Pharma Private Limited, where they contributed to quality control, documentation, and regulatory compliance initiatives.
Academic Background
Meet holds an MS in Regulatory Affairs of Drug, Biologics, and Medical Devices from Northeastern University. They have also previously worked as a Teaching Assistant at Gujarat Technological University, demonstrating their strong academic credentials and commitment to continuous learning.
Areas of Expertise
- Regulatory guidelines and compliance for pharmaceuticals, biologics, and medical devices
- Preparation and submission of regulatory documents, including applications, reports, and responses
- Quality assurance and control procedures
- Stakeholder management and cross-functional collaboration
Professional Impact
Through their internship experiences, Meet has gained valuable insights into the regulatory affairs function and has contributed to maintaining compliance and ensuring the safe and effective development of pharmaceutical and medical products. They are eager to leverage their growing expertise to make a tangible impact in the industry.
Conclusion
With a solid educational foundation, diverse internship experiences, and a keen interest in the pharmaceutical and medical technology sectors, Meet Dudhatra is poised to make valuable contributions as a Regulatory Affairs professional. They are actively seeking opportunities to further develop their skills and knowledge, and are committed to driving innovation and progress within the industry.
