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Regulatory Affairs and Quality Assurance Intern - Medical Device

JOB_REQUIREMENTS

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Roles & Responsibilities

  • Support ISO 13485 documentation
  • Assist MDR / IVDR projects
  • Maintain QMS records
  • Prepare SOP drafts
  • Prepare document trackers
  • Learn regulatory standards
  • Support senior consultants
  • Maintain document control
  • Write blogs and other marketing content

Qualification & Skills

  • Pursuing Masters' in Biomedical Engineering / Regulatory Affairs / Quality Assurance
  • Interest in Regulatory Affairs and Quality Assurance
  • Good Therotical knowledge of medical device regulations
  • Good documentation skills
  • MS Office proficiency
  • Eagerness to learn

Job Type: Internship
Contract length: 6 months

Pay: ₹5,000.00 - ₹8,000.00 per month

Work Location: In person

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