Supplier Quality Performance Specialist
Johnson & Johnson Innovative Medicine
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Benefits offered by this job
Job summary
Johnson & Johnson Innovative Medicine seeks a Supplier Quality Performance Specialist in a hybrid role based in Ringaskiddy, Ireland. You will manage systems to monitor supplier quality performance, analyze data, and drive improvements across QA processes while preparing for regulatory readiness and audits.
The role partners with Quality, Compliance, IT and business stakeholders to enable data-driven decisions and strengthen SPM transparency in a regulated environment.
Qualifications
- Bachelor’s degree in Engineering, Quality, Data Analytics, Information Systems, Life Sciences or related discipline.
- Advanced degree in Analytics, Quality or related field (preferred).
- Minimum 6 years of experience in Quality Engineering, Quality Systems, Data Analytics, Compliance, or related roles.
- Hands-on experience developing and maintaining metrics dashboards and reports.
- Experience in 21 CFR 820 / MDD / ISO 13485 environments.
- Strong analytical skills and ability to translate data into insights.
- Experience supporting audits, inspections, and management reviews with data.
Responsibilities
- Develop, maintain, and enhance metrics dashboards and reports to support QMS performance and compliance.
- Gather feedback and implement improvements to SPM procedures.
- Analyze quality data to identify trends, risks, and improvement opportunities.
- Support governance of QMS processes with accurate data reporting.
- Partner with Quality, Compliance, and IT to define data requirements and ensure data integrity.
- Support audit/inspection readiness with quality metrics and analytics.
- Maintain documentation and reporting standards for quality analytics and systems.
- Drive continuous improvement to enhance SPM transparency and metric maturity.
- Communicate verification/monitoring results to management through reviews.
Skills
Education
Tools
Job description
Hybrid - Ringaskiddy, Municipal District of Carrigaline, Ireland · Ursenbach, Bern (de), Switzerland · Zuchwil, Solothurn (de), Switzerland · Leeds, England, United Kingdom · Palm Beach Gardens, Florida, United States · Warsaw, Indiana, United States · Raynham, Massachusetts, United States · West Chester, Pennsylvania, United States
Aug 14, 2026
$94,000 - $151,800/year
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Quality
Professional
Leeds, West Yorkshire, United Kingdom, Oberdorf, Basel-Country, Switzerland, Palm Beach Gardens, Florida, United States of America, Raynham, Massachusetts, United States of America, Ringaskiddy, Cork, Ireland, Warsaw, Indiana, United States of America, West Chester, Pennsylvania, United States of America, Zuchwil, Switzerland
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 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.
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 data‑driven decision‑making, improve Supplier Performance Monitoring effectiveness, and support regulatory readiness across the organization.
- 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.
- Bachelor’s degree in Engineering, Quality, Data Analytics, Information Systems, Life Sciences, ora relateddiscipline (required).
- Advanced degree in Analytics, Quality, ora relatedfield (preferred).
- 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 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.
- 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).
- Travel:Limited; occasional domestic travel.
Coaching, Communication, Compliance Management, Controls Compliance, Cross-Functional Collaboration, Data Compilation, Econometric Models, ISO 9001, Issue Escalation, Performance Measurement, Problem Solving, Quality Control (QC), Quality Standards, Standard Operating Procedure (SOP), Technologically Savvy, Vendor Selection
$94,000.00 - $151,800.00
Additional Description for Pay Transparency:
Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 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 period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits
Johnson & Johnson Innovative Medicine leads in scientific advancements, developing transformative treatments with compassion to address complex diseases and improve patient lives worldwide.
Pharmaceutical Manufacturing Chemical Manufacturing Manufacturing
Company size 10,001+ employees
Company type Privately held
Momentum
5% in 12 mo
38,463 employees on LinkedIn
Feb 23 Apr 26
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