Valeant Pharmaceuticals

  • Quality Systems Manager

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

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




    • Works with the business to identify opportunities for improvement in business operations and processes. 
    • Involved in the design or modification of Global Quality Systems, processes, and/or IT systems. 
    • Gathers, documents, and analyzes business needs and requirements. 
    • Solves business problems and, as needed, designs technical solutions to ensure an efficient, effective and compliant Quality System.
    • Documents the functional and, sometimes, technical design of the system.
    • Interacts with system architects and developers to ensure IT systems are properly implemented. 
    • Helps test the system and create system documentation and user manuals.
    • Drive processes and tools harmonization within the business ensuring best practices are established and standardized throughout the Valeant Global Quality System.
    • Project management to drive prioritized initiatives through implementation.
    • Shape and implement a roadmap for Global Quality Systems and processes, ensuring alignment within the strategic portfolio
    • Define and implement harmonized and standardized processes across the Valeant businesses to drive business and departmental results.



    Key Relationships: Individual contributor working with the Quality Leadership team to establish and maintain an effective, efficient and compliant Global Quality System.




    • Bachelor's Degree required with preference in Quality Operations, or equivalent/Advanced degree/MBA preferred
    • Minimum Eight (8) years of relevant experience required in medical device and pharmaceutical manufacturing organizationStrong preference for expertise in Medical Device manufacturing.
    • Project management experience, including scoping, planning, execution and resource management
    • Experience with Process Excellence/Six Sigma tools, training and/or certification is required
    • Highly proficient with Microsoft Excel, Word, Power Point, Project and Access Required
    • Ability to lead and influence required
    • Experience successfully implementing change across multiple organizations with cross functional stakeholders is preferred
    • Familiar with best practices, benchmarks and latest trends regarding business plan processes preferred
    • Ability to develop, master and maintain complex technology skills, with demonstrated experience as a subject matter expert is required
    • Global experience is preferred
    • This position will require up to 30% travel both domestic and international
    • Strong technical writing skills



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