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


    Be Aware of Recruiting Fraud

    Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.


    To learn more please read Valeant’s Job Offer Fraud Statement.



    Valeant Pharmaceuticals International, Inc. is committed to leveraging the talent of a diverse workforce to create great opportunities for our business and our people. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.


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