Bausch Health

  • Sr Quality Systems Specialist (Global quality system design and modification)

    Location US-NJ-Bridgewater
    Job ID
    12284
    Category
    Quality
    Pos. Type
    Full Time
  • Overview

    The Quality Systems Specialist will use analytical, technical and organizational skills and experience to facilitate the identification and implementation of process and systems improvements in a rapidly growing and evolving regulated business.

     

    Responsibilities

    The Quality Systems Specialist will:

     

    Main Responsibilities:

    • Be involved in the design or modification of Global Quality Systems processes
    • Create procedures and other process documentation as needed for the Global Quality System.
    • Drive / lead implementation of Global processes

    Other Responsibilities:

    • Advise / participate in non-conformance, CAPA’s, Investigations, & Change Controls
    • Work with the business to identify opportunities for improvement in business operations and processes.

    Solve business problems and, as needed, assists with technical solutions to ensure an efficient, effective and compliant Quality System.

     

    Individual contributor working with the Global Quality Systems team to establish and implement an effective, efficient and compliant Global Quality Management System.

    Qualifications

    • Bachelor's Degree or equivalent experience in the Medical Device or Pharmaceutical industry
    • Minimum 5 years of relevant experience required
    • Highly proficient with Microsoft Excel, Word, Power Point, Project and Access Required
    • Ability to influence required
    • Experience successfully implementing change across multiple organizations with cross functional stakeholders is preferred
    • Familiar with pharmaceutical / medical device best practices, benchmarks and latest trends preferred
    • Global experience is preferred
    • This position may require up to 10% travel
    • Strong technical writing skills

    Minimum 5 years of experience in a pharmaceutical / medical device manufacturing and/or Quality System organization.

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