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Job Description Summary

Manages systems and processes to conduct effective Supplier Performance Monitoring (SPM) and Management across the organization. Supports day-to-day direction and improvement of the Source Quality organization's quality metrics systems. Ensures that processes, products, and services comply with established company and regulatory standards and partners with cross-functional departments in implementing quality procedures. Identifies ongoing quality and/or service issues and develops corrective and preventative action plans in response. Directs workflow to implement strategies designed to ensure Quality Systems are in line with internal best practices and in compliance with the organization’s Quality Assurance (QA) standards, international standards, and government regulations. Coordinates assignments for processes that ensure effective deployment and monitoring of Quality Systems. Contributes to meetings and aligns with multiple functions on overall Quality strategy, updates, and processes.

Job Description

DePuy Synthes is recruiting fora Supplier Quality Performance Specialist.

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.

Job Overview

Under limited supervision and in accordance with all applicable federal, state, and local laws/regulations and DePuy Synthes procedures and guidelines, the Source Quality Systems Specialist is responsible forsupporting Source and Supplier Quality Systems through advanced data analytics, reporting, and system enablement. This role plays a keypartin strengthening visibility, governance, and performance of quality processes by translating quality data into actionable insights. The position partners closely with Quality Engineering, Compliance, IT, and business stakeholders to enable datadriven decisionmaking, improve Supplier Performance Monitoring effectiveness, and support regulatory readiness across the organization.

Key Responsibilities

• • Develop,maintain, and enhance metrics dashboards and reports to support Quality Management System (QMS) performance and compliance monitoring.
  • Gather feedback from users and stakeholders and implement improvements to the SPM procedures and processes.
  • Analyze quality and compliance data toidentifytrends, risks, and improvement opportunities.
  • Support governance and execution of QMS processes throughaccurate,timely, and reliable data reporting.
  • Partner with Quality, Compliance, and IT teams to define data requirements and ensure data integrity across quality systems.
  • Support audit andinspectionreadiness by providing quality metrics, dashboards, and analytical insights.
  • Maintain documentation and reporting standards related to quality analytics and systems.
  • Drive continuous improvement initiatives to enhance SPM transparency, efficiency, and metric maturity.
  • Ensure results of verification and monitoring of the effectiveness of the quality system related to supplier performance monitoring and its compliance to applicable regulations and standards for assessing suitability, adequacy and effectiveness of quality systems are routinely communicated to management through the management review process.

Qualifications

Education:

• • Bachelor27s degree in Engineering, Quality, Data Analytics, Information Systems, Life Sciences, ora relateddiscipline (required).
  • Advanced degree in Analytics, Quality, ora relatedfield (preferred).

Experience and Skills:

Required:

• • A minimum of 6 years of experience in Quality Engineering, Quality Systems, Data Analytics, Compliance, or related roles within a regulated industry.
  • Handson experience developing andmaintainingmetrics dashboards and reports.
  • Experience within a 21 CFR 820 and/or MDD and/or ISO 13485 environment.
  • Strong analytical skills with the ability to translate complex data into clear insights.
  • Experience supporting audits, inspections, and/or management reviews with data and metrics.
  • Strong attention to detail, documentation, and data governance practices.

Preferred:

• • Experience in medical devices, healthcare, or other highly regulated industries.
  • A working knowledge medical device regulations and Quality Management Systems is desired.
  • Experience working in a global or matrixed organization.
  • Exposure to executivelevel quality reporting or metric governance.
  • Quality, Analytics, or Regulatory certifications (e.g., ASQ, RAC, Power BI certifications).

Other:

• • Language: Englishrequired.
  • Travel:Limited; occasional domestic travel.

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The anticipated base pay range for this position is :

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