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プロフィール詳細
Anil I.に依頼
India
Medical Device Quality & Regulatory Specialist | ISO 13485 | EU MDR | CAPA | Validation
プロフィール概要
専門分野
サービス
Writing
Clinical Trial Documentation,
Medical Writing,
Non-Medical Regulatory Writing
Consulting
Healthcare Consulting,
Operations Consulting,
Regulatory Consulting,
Manufacturing Consulting
Product Development
Stability/Shelf Life Testing,
Material Sourcing,
Product Validation,
Quality Assurance & Control (QA/QC),
Product Compliance ,
Packaging Design,
Reverse Engineering,
Device Fabrication
職務経験
Supplier Quality Engineering Lead - Manufacturing Transfer
Philips Healthcare
8月 2023 - 10月 2024
Project Engineering Team Lead - EU MDR & CAPA Remediation
Johnson and Johnson
12月 2021 - 7月 2023
Sr. Quality Engineer - New Product Introduction / CSV
Flextronics
5月 2021 - 12月 2021
Supplier Quality Engineer -Manufacturing Transfer
Medtronic
8月 2017 - 4月 2021
学歴
Ms in engineering technology
University of North Texas
8月 2015 - 5月 2017
認定資格