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**Supplier Quality Assurance Manager

2 months ago


Des Plaines, Illinois, United States Abbott Laboratories Full time
About the Role

This is a challenging and rewarding opportunity to lead the Supplier Quality Assurance Team at Abbott Laboratories, a global healthcare leader. As a key member of our Quality Assurance Group, you will be responsible for ensuring the highest standards of quality and compliance in our supply chain.

Key Responsibilities
  • Manage the development and administration of departmental activities related to Supplier Assurance, ensuring compliance with relevant quality assurance programs, policies, processes, and controls.
  • Lead the Supplier Quality Operations team, ensuring timely and effective implementation of quality assurance initiatives.
  • Develop and maintain departmental budgets, ensuring expenses are managed within budget while meeting established objectives.
  • Define, justify, acquire, and implement inspection test equipment to meet specified needs.
  • Re-deploy employees as priorities change to meet Division objectives.
  • Develop, train, implement, and continuously approve department policies and procedures.
  • Ensure departmental compliance with Division SOPs and procedures.
  • Provide routine communications with department employees to assure awareness.
  • Provide timely performance and developmental evaluations of departmental staff.
  • Assess and develop employee skillsets to assure effective support.
  • Work cross-functionally in identifying and resolving technical issues.
  • Provide routine department objectives and performance metrics reporting to management as defined.
  • Hire and retain a diverse, highly qualified staff and provide ongoing performance feedback.
  • Maintain a safe and professional work environment.
Requirements
  • Bachelor's Degree or related field or an equivalent combination of education and work experience.
  • Minimum 5 years related to supplied product quality within an FDA/ISO certified environment.
  • Multi-tasks, prioritizes, and meets deadlines in a timely manner.
  • Strong organizational, planning, and follow-up skills and ability to hold others accountable.
  • Travel up to 30-50%.
  • Minimum experience 7+ years managerial experience in an FDA regulated environment including IVD and/or Medical Devices.
  • Experience interfacing with FDA and ISO auditors a must.
  • ISO 13485 Certified Lead Auditor experience required.
  • Responsibility includes implementing and maintaining Supplier Control metrics.
  • Prepare and present metrics in management review meetings.
  • Experience in Purchasing Controls/Supplier Quality.
Preferred Qualifications
  • Strong leadership skills to motivate and enable department employees in meeting objectives.
  • Strong written and verbal communication skills.
  • Experience in departmental budgeting and supervision/training/managing staff.
  • At least 5 years of experience in Purchasing Controls/Supplier Quality.
  • Experience with computers and software application knowledge consistent with engineering environments.
  • Experience working in a broader enterprise/cross division business unit model preferred.
  • Ability to work in a highly matrixed and geographically diverse business environment.
About Abbott Laboratories

Abbott Laboratories is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals, and branded generic medicines.

We are committed to employee diversity and offer a range of benefits to support our employees' well-being and career development.