Senior Director, Quality TECA

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Quality

R&D/Scientific Quality

People Leader

West Chester, Pennsylvania, United States of America, Zuchwil, Switzerland

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals.

Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes, and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes.

DePuy Synthes is a global leader in Orthopaedics, advancing patient care through innovative solutions across joint reconstruction, trauma, spine, sports medicine, and related surgical technologies. As DePuy Synthes separates from Johnson & Johnson to become the world’s largest, most comprehensive Orthopaedics-focused company, the organization is entering a defining chapter—establishing its own corporate identity, voice, culture, and reputation while continuing to serve patients, customers, and healthcare systems around the world.

Senior Director, Quality TECA will be accountable for the development, execution, and delivery of quality strategies for DS TECA lifecycle management (LCM) and new product introduction (NPI) engineering activities.

• Acts as the Quality Management Representative for Synthes West Chester, PA sites:
  Headquarters, Technology Center, and Wilson Drive Development Center.

Under limited supervision and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Will be a member of DS TECA Platform Operating Committee and will provide the quality strategic vision for the organization.
• Will provide guidance and coaching to all levels within the Quality organization and Quality leadership for the business.
• Will partner with R&D, Supply Chain, Regulatory & Marketing to assure all LCM/NPI engineering and quality deliverables are met within quality, cost, and schedule targets.
• Will partner with R&D, Supply Chain, Regulatory & Marketing to assure there is appropriate execution of risk management, design controls and process validation for new and existing products.
• Will manage overall quality budget, ensuring effective allocation of resources and investments to achieve quality objectives.
• Will be accountable for quality metrics to identify systemic product and process issues assuring appropriate investigation, correction, and corrective and preventive action when needed.
• Will be responsible for the Synthes Quality Management Review.
• Will support Quality related activities for product issue escalation, investigations (PIE/PIA) and QRB.
• Will partner with Supplier Quality and Manufacturing, to ensure Quality…