Job Description

Job Title: Graduate Trainee - Medical Device Regulatory Affairs

Company Overview

Morulaa Healthtech Pvt. Ltd. is a Chennai-based consulting firm specializing in global medical device registration and regulatory compliance. We assist medical device manufacturers, importers, and innovators worldwide in achieving market approvals by providing end-to-end support in regulatory submissions, documentation, and certification.

Position Summary

We are seeking fresh graduates (B.Tech / B.E. in Biomedical Engineering or Biotechnology) who have completed their schooling and graduation from reputed and accredited institutions.
This role is ideal for candidates who aspire to build a career in medical device regulatory affairs, documentation, and compliance consulting. Selected candidates will undergo structured training on international regulatory frameworks and quality management systems.

Key Responsibilities

Assist in the preparation, review, and submission of technical documentation for medical device registrations. Support consultants in global regulatory submissions (CDSCO, US FDA, EU MDR, MHRA, TGA, ASEAN, GCC, etc.). Conduct regulatory research to interpret and apply country-specific compliance requirements. Coordinate with clients to collect technical data, reports, and product certifications. Help develop and maintain Standard Operating Procedures (SOPs) and quality documentation (ISO 13485, GMP). Maintain organized records of submissions, approvals, and regulatory correspondence.

Qualifications

B.Tech / B.E. in Biomedical Engineering or Biotechnology. Must have completed schooling and graduation from reputed institutions with a consistent academic record. Excellent written and verbal communication skills. Strong attention to detail, analytical ability, and documentation skills. Keen interest in regulatory affairs, compliance, and healthcare technology.

Preferred Skills

Proficiency in MS Office (Word, Excel, PowerPoint) and internet-based research. Ability to work collaboratively and meet strict documentation timelines.

What We Offer

Comprehensive training in global medical device regulatory systems. Exposure to international registration projects and real-world regulatory workflows. Mentorship from senior consultants and domain experts. A structured career path in regulatory affairs, quality systems, or global compliance. A professional and learning-driven environment that values precision and integrity.

Location

Chennai, Tamil Nadu (Office-based role).

How to Apply

To Apply: Please send your CV to mail id- team.support7@morulaa.com & Whatsapp number-+91 8610467854

Job Types: Full-time, Permanent, Fresher

Pay: ?250,000.00 - ?300,000.00 per year

Benefits:

Food provided Paid time off Provident Fund
Work Location: In person