Bausch Health

  • Sr. Supplier Quality Specialist

    Location US-MO-St Louis
    Job ID
    Pos. Type
    Full Time
  • Overview

    Responsible for Supplier Quality Assurance activities for existing supply base, including maintenance of business (MOB) and cost improvement projects (CIP)   at the surgical business unit including, but not limited to:  product sourcing decision support; advance product quality planning; suppliers assessment/audits and qualification;  validation of supplier processes; qualification of services, parts and/or finished products; and managing supplier corrective action activities and concern resolution process leadership.


    Additionally, may function in the same capacity to support some new design  projects.


    Represent Supplier Quality in internal project meetings and manufacturing readiness reviews and leads supplier on multiple Quality deliverables for existing supply base.


    Acts as the Supplier Quality liaison between Manufacturing, Manufacturing Engineering, Purchasing, Operations Quality, and the supplier.


    Supports purchasing and operations with source identification, evaluation and selection. Leads On-Site Assessments and supplier risk assessments of existing and potential new suppliers.


    Coordinates supplier activities necessary to fulfill B+L general and specific requirements for product/service qualification such as First Article Inspection, receiving inspection processes, supplier process controls, capability studies for critical product characteristics and implementation of PFMEAs and Control Plans, process validation, among others in support of current supply base.


    Develop and maintain local supplier management procedures to ensure that regulatory, local and corporate requirements are met.    Review and provide input to new/revised corporate procedures that impact the site.


    Perform supplier audits for new and existing suppliers to assure products/services meet the requirements of applicable ISO standards, regulations, product specifications and B+L local and corporate requirements. 


    Responsibilities may include up to 25% travel.


    Reviews and approves supplier-related/initiated Change Notices and documentation for existing product revisions/line extensions and/or services.


    Ensures resolution of supplier related quality problems, including internal failures, customer complaints and audit findings by managing nonconforming product disposition, supplier investigation of root cause, corrective action planning, implementation, and verification of effectiveness activities.


    Establishes, reports, and sustains key supplier quality performance metrics and corresponding training, improvements and reporting responsibilities.


    Ensure supplier documentation is maintained including risk assessments, quality agreements, and quality system certifications.


    Supports costs of quality reduction goals and supplier risk mitigation activities.


    Authoring, reviewing and implementation of policies and procedures, to drive supplier quality improvement processes for continuous improvement.


    The scope of the position is primarily focused on suppliers for existing supply base with extended scope to support supplier quality issues affecting new product development activities.


    Required Education:


    BS in Engineering, Biology, Chemistry (or equivalent experience)

    Preference given to degreed engineers or technical degree type.


    Required Skills/Qualifications:


    Excellent verbal and written communication skills.  Ability to prioritize multiple tasks and projects with limited direct supervision.  Effective organization and negotiation skills.  Strong ability to manage suppliers, follow-up and complete projects.  Proficient in MS Office Applications


    Required Experience:


    5+ years’ Quality experience in the Medical Device Manufacturing industry; 3+ years in supplier quality related processes.  Must have proven and results-driven track record of successfully managing projects, people and suppliers.  Responsible for developing & implementing quality processes in a global business environment, including supplier manufacturing sites.


    Preferred Experience:

    Additional consideration for experience in other regulated industries (automotive, aerospace, etc.).  and for the following certifications:  ASQ CQE, CQA, CQM and Six Sigma Green Belts, Black Belts, and Master Black Belts.  


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