Quality and Regulatory Intern

0 - 1 years

2 - 3 Lacs

Posted:10 hours ago| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

Education Qualification

  • Execute required activities as part of ISO 13485 and ISO 15189 compliance
  • Undertake activities as part of manufacturing documentation under ISO 13485
  • Undertake activities in molecular kit development and kit packaging departments
  • Preparation of regulatory document dossier

Requirements

  • The candidate must have the ability to execute tasks and document information independently.
  • Have a basic understanding of quality assurance and quality checks
  • Awareness of ISO 13485 and ISO 15189

Skills

  • Keen attention to details.
  • Ability to critically evaluate scientific literature and integrate information from multiple sources.
  • Proficiency in Google & Microsoft Office Suite and other relevant software applications.
  • Ability to work independently with minimal supervision as well as collaboratively in a team environment.
  • Excellent organizational and time management skills with the ability to prioritize tasks effectively
  • Strong interpersonal and communication skills with the ability to interact professionally with diverse stakeholders

Note:

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