V-REG Hiring Regulatory Interns

V-REG Hiring Regulatory Interns | Life Sciences & Pharmacy

Apply for Regulatory Internship at V-REG Solutions. Open to life sciences, pharmacy & biomedical graduates with interest in medical device regulations.

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V-REG Solutions, a specialized regulatory services company, is inviting applications for Regulatory Intern (Level I) positions. This internship is designed for candidates from life sciences, biomedical sciences, and pharmacy backgrounds who are passionate about regulatory affairs in the medical device sector. It’s an excellent opportunity to gain hands-on exposure to global regulatory frameworks (India, US FDA & EU) while working with a highly supportive and experienced team.

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Company Overview

V-REG Solutions is a trusted partner in the field of medical device regulatory consulting, offering expert support in ISO standards, QMS, technical file preparation, and licensing services. The company collaborates with clients worldwide to ensure compliance with India, EU, and US FDA regulations. With a focus on mentoring and skill development, V-REG provides interns with the right platform to begin their careers in regulatory affairs.

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Job Role & Responsibilities

Regulatory Intern – Level I

• Experience: Internship role (Freshers eligible)
• Qualification: Life Sciences, Biomedical, or Pharmacy background
• Key Responsibilities:
  • Assist in technical file preparation and regulatory documentation.
  • Support quality management system (QMS) processes under ISO 13485 standards.
  • Conduct research on medical device regulations across different geographies.
  • Provide assistance in licensing and compliance activities.
  • Collaborate with senior regulatory professionals in a team-oriented environment.

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Eligibility / Qualifications

• Required Education: B.Sc/M.Sc Life Sciences, Biomedical Sciences, B.Pharm, M.Pharm.
• Skills Required:
  • Basic understanding of ISO 13485 Standard.
  • Proficiency in MS Office (Excel, PowerPoint, Word).
  • Good writing, research, and documentation skills.
  • Strong interest in medical device regulations.

Relevant courses: B.Sc Biotechnology, M.Sc Biotechnology, B.Pharm, M.Pharm, B.Sc Biomedical, M.Sc Biomedical, M.Sc Microbiology, M.Sc Regulatory Affairs.

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Location & Salary

• Work Location: V-REG Solutions (Remote/Hybrid opportunities may be available depending on project needs).
• Stipend/Perks: Mentorship from senior regulatory experts, exposure to global regulatory frameworks, hands-on experience in QMS, licensing, and compliance.

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Application Process

Interested candidates should send their updated CVs to the official recruitment email.

Email: info@vregsolutions.com
Website: www.vregsolutions.com

Apply at the earliest to secure your chance to start a career in medical device regulatory affairs with V-REG.

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FAQs

1. Who can apply for the internship?
Students or graduates from Life Sciences, Biomedical, or Pharmacy backgrounds.

2. Is prior experience required?
No, freshers with interest in regulatory affairs are eligible.

3. What standards should interns be familiar with?
Basic knowledge of ISO 13485 is desirable.

4. What skills are most valued?
Documentation, research, MS Office skills, and an interest in regulatory compliance.

5. What are the internship perks?
Mentorship, exposure to global regulations, and practical training in QMS and licensing.

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Summary Table

Category	Details
Company	V-REG Solutions
Vacancies	Regulatory Intern (Level I)
Required Education	B.Sc/M.Sc Life Sciences, Biomedical, B.Pharm, M.Pharm
Experience	Internship (Freshers eligible)

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