Data Entry

Boston, MA

Responsibilities

 

  • Perform data entry and formulate reports / graphs associated to special projects, complaints and lot qualification.
  • Uphold accurate documentation and files related to special projects, complaints and lot qualification.
  • Review and evaluate lot documentation (DHR’s) to determine if there are any irregularities that may have related to reported product failures.
  • Support database development and reporting capabilities related to the complaint / reliability department needs.
  • Process feedback letters and communicate to product support managers for various reporting sites.
  • Take part in basic product review and failure analysis.
  • Assist in gathering information and data during FDA, ISO or other third party or internal audits.
  • Help with the investigation and review of potential opposing events.
  • Assist with Post market surveillance reporting (MDRs, MDVs, MDPRs, etc.).

 

Requirements

 

  • Associates Degree
  • Minimum of 0-3 years’ experience with data management, record keeping, and trouble shooting in the Medical Device field, or other transferable experience related to organization, technical aptitude and data management.
  • Effective verbal and technical writing skills.
  • Ability to organize and judge priorities.
  • Excels at generating and maintaining organized and accurate records.
  • Able to work effectively in a high-stress, high-energy environment.

 

 

 

Note: Qualified candidates will be contacted within 2 business days of application. If an applicant does not meet the above criteria, we will keep your resume on file for future opportunities and may contact you for further discussion.

Date Posted 9/10/2019
Salary $20.00/hr






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