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4 Maven Profcon Services Jobs
Regulatory Affairs Intern
Maven Profcon Services
posted 4d ago
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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.
Employment Type: Full Time, Permanent
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