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Quality Specialist

San Diego  ‐ Onsite
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Description

Qualifications:
  • Bachelor's degree in associated field (e.g. Technical Writing, Creative Writing, Communications, etc) or technical degree with 2+ years working experience as a technical writer or similar
  • Previous experience in the development and/or execution of Medical Device Quality System Regulations (i.e. FDA QSR, ISO 13485)
  • Prior experience creating documents, procedures, and training material that support multiple elements of a medical device Quality System preferred
  • Prior project management experience preferred


    • Responsibilities:
  • Work with SMEs and other key stakeholders to gather documentation requirements for multiple elements of a Medical Device Quality System
  • Create clear and concise Global Quality System Standards and Procedures to promote consistent, repeatable compliance based on requirements gathered from key SME stakeholders
  • Create a document structure and templates that can be used as the framework for a set of global Standards and Procedures
  • Assist in the design, develop and deliver of training programs (e.g. e-learning, classroom) in support of the global business processes and IT solution
  • Ensure grammatical and spelling accuracy
  • Work with SME team to ensure technical content is clear, concise and easy to follow
    • Start date
    06/2014
    Duration
    12 months
    From
    Real Staffing
    Published at
    07.06.2014
    Project ID:
    722679
    Contract type
    Freelance
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