Supplier Quality Analytics Lead

jj; Raynham (MA); On-site; USD 94,000 - 152,000; Full time

Job summary

DePuy Synthes, a Johnson & Johnson company, seeks a Supplier Quality Performance Specialist in Raynham, MA to drive data‑driven supplier quality monitoring and analytics. You will develop dashboards, monitor quality metrics, and partner with cross‑functional teams to ensure compliance with regulatory standards.

The role emphasizes ownership of quality analytics, readiness for audits, and continuous improvement of SPM processes within a regulated medical devices environment.

Qualifications

• Bachelor’s degree in Engineering, Quality, Data Analytics, Information Systems, Life Sciences, or related discipline (required).
• Advanced degree in Analytics, Quality, or related field (preferred).
• Experience in a regulated industry with data analytics and quality systems.

Responsibilities

• Develop, maintain, and enhance metrics dashboards and reports for QMS performance and compliance monitoring.
• Gather feedback from users and stakeholders; implement improvements to SPM procedures and processes.
• Analyze quality data to identify trends, risks, and opportunities for improvement.
• Support governance and execution of QMS processes with reliable data reporting.
• Partner with Quality, Compliance, and IT to define data requirements and ensure data integrity.

Skills

Quality Engineering

Data Analytics

Regulated industry

Quality dashboards

Audit readiness

Cross-functional collaboration

Education

Bachelor’s degree in Engineering/Quality/Data Analytics

Advanced degree in Analytics/Quality

Tools

Power BI

Quality Management Systems

Job description

DePuy Synthes, a Johnson & Johnson company, seeks a Supplier Quality Performance Specialist in Raynham, MA to drive data‑driven supplier quality monitoring and analytics. You will develop dashboards, monitor quality metrics, and partner with cross‑functional teams to ensure compliance with regulatory standards.

The role emphasizes ownership of quality analytics, readiness for audits, and continuous improvement of SPM processes within a regulated medical devices environment.