Staff Source Quality Engineer

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions 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. Job Function Supply Chain Engineering Job Sub Function Quality Engineering Job Category Scientific/Technology All Job Posting Locations Guaynabo, Puerto Rico, United States of America; Raritan, New Jersey, United States of America Job Description About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Learn more at Staff Source Quality Engineer The Staff Source Quality Engineer provides global Source Quality leadership for direct and indirect suppliers and external manufacturers supporting Johnson & Johnson products. This role leads the deployment and execution of Source Quality Management strategies, supplier controls, and risk‑based quality oversight to ensure supplier qualification, performance, change management, issue resolution, and continuous improvement are conducted in alignment with applicable regulatory requirements, quality system standards, and business objectives. The Staff SQE partners with suppliers and cross‑functional stakeholders to strengthen supplier capability, prevent quality and compliance risks, and support a reliable, compliant, and resilient supply base for Ethicon Supply Chain suppliers. Key Responsibilities Provide global Source Quality Management support by leading supplier and purchasing controls, including supplier selection, qualification, monitoring, change management, and Approved Supplier List management. Partner with suppliers and cross‑functional stakeholders to investigate, resolve, and prevent supplier‑related quality issues, minimize business disruptions, and support robust materials, products, processes, and systems. Monitor supplier performance, analyze quality data and trends, communicate risks, and drive quality risk management, corrective actions, targeted improvements, and supplier relationship management activities. Lead supplier quality projects, component qualification changes, quality agreements, and process/product improvement initiatives using project management, Quality Engineering, and continuous improvement tools. Ensure compliance with applicable quality system, regulatory, environmental, health, safety, and company requirements while communicating business issues and opportunities to management. Qualifications Education A bachelor’s degree in Engineering, Applied Science, or a related technical or quality field required. Experience and skills Minimum of 6 years in a highly regulated industry, with manufacturing, engineering and/or quality work experience. Demonstrated ability to assess compliance risks and business impact, manage complexity, influence diverse teams, and resolve complex issues using deductive reasoning, critical analysis, and systematic approaches. Working knowledge of regulatory compliance requirements, including QSRs, MDD, ISO 9001, ISO 13485, ISO 14971, or other applicable international standards. Strong business acumen and ability to collaborate with all levels of management in a cross‑functional team environment. Experience with quality issue investigations, NCRs, CAPAs, analytical tools, metrics development, trend identification, and business/software applications including Word, Excel, PowerPoint, Minitab, Visio, and Microsoft Project. Strong communication skills in English. Preferred Risk management, GxP, quality systems, supplier management, CAPA/non‑conformance, technical writing, audit, component or process validation experience is preferred. Relevant certifications or training, such as ASQ CQE, CQM, CSQP, CQA, CBA, FPX, PMP, Six Sigma Black Belt/Green Belt, Lean, PE leadership training. Other This position may require up to 25% of domestic and/or international travel. Required Skills Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, Good Automated Manufacturing Practice (GAMP), ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy Preferred Skills Coaching, Consistency, Controls Compliance, Critical Thinking, Data Savvy, Engineering, Financial Competence, Good Automated Manufacturing Practice (GAMP), ISO 9001, Lean Supply Chain Management, Leverages Information, Process Improvements, Quality Control Testing, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Technologically Savvy Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource. #J-18808-Ljbffr Johnson & Johnson MedTech