Associate Quality Director

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BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of Med Tech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description
Reporting to the VP of Quality Management
, the Associate Director, Plant QA leads and directly manages technical and managerial staff at the Sumter facility. This role plays a pivotal part in shaping global quality strategy and driving the tactical execution needed to achieve organizational objectives. Through exceptional communication, proactive problem-solving, and confident navigation of ambiguity, the Associate Director ensures product safety, quality, and full compliance with global regulations and customer expectations.

Success in this role is measured by the minimization of product quality and organizational issues, as well as the continuous improvement of business process effectiveness. By fostering strong relationships with internal and external stakeholders — and investing in the growth and development of people — the Associate Director, Plant QA delivers sustainable, industry-leading results that support key business drivers.

Responsibilities:

• Quality System Champion
  - Establishing, implementing, and maintaining vital quality management processes

• Executive Quality Liaison
  - Delivering insightful performance reports to top management through Management Review meetings, highlighting improvement opportunities

• Regulatory Awareness Ambassador
  - Fostering a culture where every team member understands and embraces regulatory and customer requirements

• Inspection Point Person
  - Serving as the primary contact for FDA, ISO, and third-party audits, representing the Sumter site

• Compliance Program Overseer
  - Managing comprehensive quality activities including CAPA, Quality Notifications, Temporary Deviations, Internal and Supplier Audits, Change Control, Calibration, and Complaint Investigations.

  • This includes compliance to applicable regulations and standards for medical devices and pharmaceutical products.

• Product Release Guardian
  - Supervising laboratory operations and release personnel to ensure only safe, effective products reach customers, including on-site sterilization quality oversight

  • Responsible for approval or rejection of components, finished products, and documents to achieve this purpose.

• Strategic Leadership Team Member
  - Contributing to the Plant Leadership Team and Executive Steering Committee to drive plant initiatives and achieve organizational goals

• Quality Strategy Architect
  - Developing and maintaining forward-thinking quality plans and policies that align business objectives with regulatory requirements

• Continuous Improvement Driver
  - Directing Quality Assurance projects through leadership teams to maintain regulatory compliance and support plant continuous improvement efforts

• Talent Developer
  - Building a high-performing quality team through targeted training and professional development opportunities

• Financial Steward
  - Managing the Quality department and laboratory budget with efficiency and foresight

• Problem-Solving Partner
  - Collaborating with multi-functional teams to identify root causes of quality issues and customer complaints. Works with the Design Center Quality Management to drive investigations for product issues in the field and assists with the preparation of Situation Analyses.

• Product Development Collaborator
  - Supporting new product initiatives and facilitating smooth Design Transfer from development to…