Regulatory Affairs Intern

20 hours ago

Prahlad Nagar Ahmedabad Gujarat, India Maven Profcon Services LLP Full time

Job Description:
As a **Medical Device Regulatory Affairs Intern**, you will work alongside experienced regulatory professionals, gaining hands-on experience in regulatory submissions, compliance research, and documentation for medical devices.

Key Responsibilities:

- Assist in preparing regulatory documentation for product registrations and submissions.
- Conduct research on international medical device regulations (EU MDR, US FDA, etc.).
- Support the compilation and maintenance of technical files and regulatory reports.
- Review and update regulatory compliance databases.
- Assist in writing and editing regulatory documents, reports, and summaries.
- Coordinate with cross-functional teams to gather necessary regulatory information.
- Monitor regulatory changes and updates to ensure compliance.

**Requirements**:

- Currently pursuing or recently completed a degree in Biomedical Engineering,Biotechnology or Regulatory Affairs, or a related field.
- Strong interest in medical device regulatory affairs and compliance.
- Excellent research and analytical skills.
- Strong written and verbal communication skills.
- Attention to detail and ability to manage multiple tasks.

**Job Type**: Internship
Contract length: 6 months

Pay: ₹5,000.00 - ₹8,000.00 per month

Schedule:

- Day shift

Ability to commute/relocate:

- Prahlad Nagar, Ahmedabad, Gujarat: Reliably commute or planning to relocate before starting work (required)

Work Location: In person

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