Savannah Feterl

Experience

• 

  University of Missouri-Columbia

  Aug 2020 - May 2022

  • Teaching Assistant

    Aug 2021 - May 2022

  • Writing Center Tutor

    Jan 2020 - May 2022

  • Teaching Assistant

    Aug 2020 - Dec 2020
• 

  Boston Scientific

  Oct 2022 - now

  - Manage and assist with upkeep of deliverables housed in Design History File (DHF) of multiple device projects simultaneously, including physical documents such as testing data sheets, shop floor paperwork, etc.- Own and complete a variety of quality assurance, risk management, and regulatory documents.- Organize and log product documents in online documentation control system (Windchill).- Serve as Windchill SME on project teams, facilitating training and assisting teammates with troubleshooting.- Collaborate cross-functionally with DA, R&D, Process Development, Regulatory, Clinical Risk, Marketing, functional managers, and other team members to acquire information for document completion.- Track status of deliverables and related design control activities.- Ensure documents adhere to company-wide and global quality regulations and standards, in addition to following relevant templates.- Assist with compiling regulatory submissions (PMA supplement, 510(k)) to FDA, PMDA, and Dekra. Show less - Peripheral Interventions - Design Assurance, vascular/arterial new product development space- Manage/assist with creation and upkeep of deliverables housed in Design History File (DHF) of multiple device projects simultaneously - Log product documents in online documentation control system and run change notices for documents- Collaborate closely with DA, R&D, PD, and manufacturing engineers, regulatory and clinical specialists, functional managers, and other team members to acquire data for product document completion- Track progress/status of deliverables and related design control activities- Ensure documents adhere to company-wide and global quality regulations and standards, in addition to following relevant templates- Draft and own a variety of engineering deliverables (e.g., hazard analysis matrices, design matrices, test protocols and reports, etc.)- Facilitate discussion with fellow technical writers surrounding furthering tech writing-related education and training, driving to improve and refine the tech writer role as defined in the context of the med device industry - Manage the storage of physical project-related documents such as test data sheets, shop floor paperwork, and more Show less

  • Technical Writer II

    Aug 2024 - now

  • Technical Writer I

    Oct 2022 - Aug 2024