Supplier Quality Performance Specialist

Johnson & Johnson Innovative Medicine

1d•$94,000 - $151,800•Hybrid

About The Position

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. DePuy Synthes is recruiting for a 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. 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 for supporting Source and Supplier Quality Systems through advanced data analytics, reporting, and system enablement. This role plays a key part in 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 data‑driven decision‑making, improve Supplier Performance Monitoring effectiveness, and support regulatory readiness across the organization.

Requirements

Bachelor’s degree in Engineering, Quality, Data Analytics, Information Systems, Life Sciences, or a related discipline (required).
A 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 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.
Language: English required.

Nice To Haves

Advanced degree in Analytics, Quality, or a related field (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 executive‑level quality reporting or metric governance.
Quality, Analytics, or Regulatory certifications (e.g., ASQ, RAC, Power BI certifications).

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 to identify trends, risks, and improvement opportunities.
Support governance and execution of QMS processes through accurate, 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 and inspection readiness 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.

Benefits

Consolidated retirement plan (pension)
Savings plan (401(k))
Long-term incentive program
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year
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
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year