Yantrolok is hiring a Regulatory & Quality Compliance Intern to support ISO 13485 compliance, DHF documentation, and risk management activities. This 3 to 6 months internship offers Biomedical, Electronics, Mechanical, and Instrumentation students hands-on exposure to regulatory affairs and quality management systems (QMS) in the medical device industry.
If you are looking to build a career in regulatory affairs, ISO 13485 compliance, medical device documentation, and quality assurance, this opportunity provides practical experience in Device History File (DHF) preparation and risk management processes under expert supervision.
About the Role
The Regulatory & Quality Compliance Intern will work closely with the regulatory and quality teams to ensure compliance with ISO 13485 standards and medical device regulations. The internship is available in Hybrid/Remote mode, making it accessible to candidates across India.
This internship is ideal for candidates seeking experience in:
- ISO 13485 QMS implementation
- Device History File (DHF) documentation
- Risk management for medical devices
- Regulatory compliance processes
- Quality assurance documentation
Key Responsibilities
As a Regulatory & Quality Compliance Intern, you will:
- Assist in maintaining and updating ISO 13485 Quality Management System (QMS) documentation
- Support preparation and review of Device History File (DHF)
- Participate in risk management activities as per ISO 14971
- Ensure compliance with regulatory requirements for medical devices
- Help with document control and internal audit preparation
- Collaborate with cross-functional teams (R&D, production, QA)
- Support regulatory submissions and compliance tracking
This role offers hands-on experience in medical device regulatory affairs and quality compliance practices.
Eligibility Criteria
Candidates applying for the Regulatory & Quality Compliance Internship should have:
- Bachelor’s or Master’s degree (pursuing or completed) in:
- Biomedical Engineering
- Electronics Engineering
- Mechanical Engineering
- Instrumentation Engineering
- Basic understanding of ISO 13485, QMS documentation, and medical device regulations
- Strong documentation and analytical skills
- Interest in regulatory affairs and quality assurance
- Ability to work independently in a Hybrid/Remote setup
Internship Duration
- 3 to 6 months
- Flexible engagement (Hybrid/Remote)
Benefits of This Internship
- Practical exposure to ISO 13485 compliance and QMS systems
- Real-world experience in DHF and risk management documentation
- Mentorship from regulatory and quality experts
- Industry-relevant skills in medical device regulatory affairs
- Certificate of internship upon successful completion
- Opportunity to strengthen your career in regulatory compliance and quality assurance
How to Apply
Interested candidates can apply by sending their updated resume to:
