Job Description – Regulatory Compliance Intern to Full-Time Executive
Company: MedDevices Consultancy Pvt. Ltd.
Department: Regulatory Affairs & Compliance
Location: Mohali
Internship Duration: 3 Months
Employment Type: Internship with Full-Time Opportunity
About the Company
MedDevices Consultancy Pvt. Ltd. is a leading Medical Device Regulatory & Compliance consultancy providing services related to global medical device regulations, including FDA Registration, EU Authorized Representative (EAR), UK Responsible Person, ISO 13485 compliance, CE Marking support, and international regulatory consulting for medical device manufacturers.
We are looking for enthusiastic and career-oriented candidates who are interested in building their career in Medical Device Regulatory Affairs and Compliance.
Position Overview
The Regulatory Compliance Intern will work closely with the Regulatory Affairs team to support compliance activities, documentation management, regulatory submissions, and quality system processes for medical device clients across international markets.
After successful completion of the 3-month internship, high-performing candidates may be offered a full-time role as a Regulatory Compliance Executive.
Internship Responsibilities (First 3 Months)Regulatory Documentation
- Assist in the preparation and review of technical files and regulatory documents.
- Support medical device registration documentation for US FDA, EU MDR, UKCA, and other global markets.
- Maintain regulatory records, certificates, and submission documents.
Compliance Support
- Assist in activities related to ISO 13485, CE Marking, FDA Registration, and global compliance requirements.
- Help track regulatory updates and maintain compliance databases.
- Support internal audit and documentation activities.
Research & Regulatory Intelligence
- Conduct research on international medical device regulations.
- Prepare compliance reports, summaries, and market requirement data.
- Support regulatory gap analysis activities.
Coordination & Reporting
- Coordinate with internal teams and clients for regulatory information collection.
- Maintain trackers and compliance status reports.
- Support preparation of presentations and compliance documentation.
Full-Time Opportunity After Internship Designation: Regulatory Compliance Executive
Based on internship performance, candidates may be absorbed into the full-time Regulatory Affairs team.
Full-Time Responsibilities
- Handling client regulatory projects.
- Preparing regulatory submissions and technical documentation.
- Coordinating with international regulatory authorities and clients.
- Managing compliance activities for medical device manufacturers.
- Supporting ISO 13485 and global certification processes.
Eligibility Criteria
- B.Sc / M.Sc Biotechnology
- Biomedical Engineering
- Life Sciences
- Regulatory Affairs or related fields
Freshers and recent graduates are encouraged to apply.
Required Skills
- Good communication and documentation skills
- Strong attention to detail
- Basic understanding of medical device regulations preferred
- MS Office proficiency
- Ability to work in a team environment
- Willingness to learn international compliance processes
What You Will Learn
- Medical Device Regulatory Affairs
- US FDA & EU MDR compliance
- ISO 13485 Quality Management System
- CE Marking process
- Technical Documentation preparation
- Global regulatory submission procedures
Benefits
- Industry exposure in Medical Devices & Life Sciences
- Practical training from experienced regulatory professionals
- Internship completion certificate
- Career growth opportunity in Regulatory Affairs
- Potential permanent employment after internship
Pay: Up to ₹7,000.00 per month
Work Location: In person
