プロフィール詳細

プロジェクトを作成

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Ninja P.に依頼

Canada

Regulatory Affairs Professional (Medical Device Consultant)

プロフィール概要

An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an esteemed organization, where I can use my strong knowledge, skills, and experience to contribute to Design Dossiers, MDSAP, Audit, Compliance, CAPA, Deviation reports, ISO 13485, ICH/GCP guidelines, Clinical study monitoring, SOP writing, able to prepare and file medical device applications to USFDA health and Canada. Able to do project planning for the growth of the organization.

専門分野

• ★ Medical Device Regulatory Consulting
• ☆ Medical Devices
• ☆ ISO 13485
• ☆ Regulatory Affairs
• ☆ Medical Writing

サービス

• Writing
• Product Development

Writing Technical Writing

Product Development Product Evaluation

職務経験

RA/QA Specialist

Diros Technology

6月 2023 - 現在

Regulatory affairs consultant

Q and R consulting

3月 2022 - 現在

学歴

Regulatory Affairs Medical Device

Northeastern University

9月 2021 - 6月 2022

認定資格

• Intermediate Medical Writing: Medical Devices

  RAPS

  3月 2022 - 現在