Supplier Quality Performance Specialist

Johnson & Johnson

Supplier quality specialist improving medical-device performance monitoring for Johnson & Johnson’s DePuy Synthes business. Building dashboards, analyzing compliance data, and strengthening quality-system governance and audit readiness across global stakeholders.

Posted 8/14/2026full-timeRaynham • Florida, Massachusetts, Pennsylvania • 🇺🇸 United StatesMid-LevelSenior💰 $94,000 - $151,800 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Quality Systems Management, Supplier Performance Monitoring, and Data Analytics within regulated environments. Proficient in developing metrics dashboards and ensuring compliance with industry standards and regulations.

Highest-signal resume keywords

Quality Systems ManagementSupplier Performance MonitoringData AnalyticsRegulatory ComplianceMetrics Dashboard Development

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Quality EngineeringData AnalyticsMetrics Dashboard DevelopmentQuality Management SystemsRegulatory Standards ComplianceQuality Metrics AnalysisCorrective Action PlanningProcess ImprovementAudit SupportDocumentation Standards

Soft Skills

Analytical SkillsAttention to DetailCommunication Skills

Tools & Technologies

Quality Management SystemsData Reporting ToolsMetrics DashboardsAnalytical Software

Certifications & Qualifications

ASQ CertificationRAC CertificationPower BI Certification

Industry Keywords

21 CFR 820MDDISO 13485Medical DevicesHealthcareRegulated Industry

About the role

Key responsibilities & impact

Manage systems and processes for effective Supplier Performance Monitoring (SPM) and management across the organization
Support day-to-day direction and improvement of Source Quality organization quality metrics systems
Ensure processes, products, and services comply with company and regulatory standards
Partner with cross-functional departments to implement quality procedures
Identify quality and service issues and develop corrective and preventative action plans
Direct workflow to align Quality Systems with internal best practices, QA standards, international standards, and government regulations
Coordinate process assignments for effective deployment and monitoring of Quality Systems
Develop, maintain, and enhance metrics dashboards and reports for QMS performance and compliance monitoring
Gather stakeholder feedback and improve SPM procedures and processes
Analyze quality and compliance data to identify trends, risks, and improvement opportunities
Support QMS governance and execution through accurate, timely, and reliable data reporting
Partner with Quality, Compliance, and IT teams to define data requirements and ensure data integrity
Support audit and inspection readiness with quality metrics, dashboards, and analytical insights
Maintain documentation and reporting standards for quality analytics and systems
Drive continuous improvement to improve SPM transparency, efficiency, and metric maturity
Communicate supplier performance monitoring quality-system verification and monitoring results to management through management review

Requirements

What you’ll need

Bachelor’s degree in Engineering, Quality, Data Analytics, Information Systems, Life Sciences, or a related discipline (required)
Minimum of 6 years of experience in Quality Engineering, Quality Systems, Data Analytics, Compliance, or related roles within a regulated industry
Hands-on experience developing and maintaining metrics dashboards and reports
Experience within a 21 CFR 820 and/or MDD and/or ISO 13485 environment
Strong analytical skills 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
English required
Limited travel; occasional domestic travel
Preferred: experience in medical devices, healthcare, or other highly regulated industries
Preferred: working knowledge of medical device regulations and Quality Management Systems
Preferred: experience in a global or matrixed organization
Preferred: exposure to executive-level quality reporting or metric governance
Preferred: Quality, Analytics, or Regulatory certifications such as ASQ, RAC, or Power BI certifications

Benefits

Comp & perks

Participation in the Company’s consolidated retirement plan (pension)
Savings plan (401(k))
Eligibility for the Company’s long-term incentive program
Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year; 48 hours per calendar year for employees who reside in Colorado; 56 hours per calendar year for employees who reside in Washington
Holiday pay, including Floating Holidays – 13 days per calendar year
Work, Personal and Family Time – up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
10 days Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year