Mgr Supplier Quality

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 . 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. Job Function: Quality Job Sub Function: Supplier Quality Job Category: Professional All Job Posting Locations: Shanghai, China Job Description:

Provides leadership and oversight for Product Quality, Supplier Quality Management, Purchasing Controls, Manufacturing Quality (incl. Product Release), and Quality System activities within J&J Med Tech Neurovascular China and the assigned supplier quality scope. This role ensures products, suppliers, subcontractors, processes, and services comply with applicable Johnson & Johnson requirements, regulatory expectations, and industry standards. The position drives supplier performance, quality risk management, audit readiness, continuous improvement, and effective Quality System execution while communicating significant quality risks and opportunities to management.

Under limited supervision and in accordance with applicable laws, regulations, Johnson & Johnson procedures, and guidelines, this position: Oversee Supplier Quality Management, Purchasing Controls, Manufacturing Quality, Product Release, and Quality System activities within the assigned scope. Develops and maintains risk-based supplier quality strategies, including supplier selection, qualification, monitoring, performance management, and supplier corrective actions. Provides oversight of suppliers, subcontractors, and external service providers to ensure compliance with approved agreements, procedures, training, and quality requirements. Reviews and approves manufacturing and sterilization records and authorizes product release, as assigned. Leads or supports corrective and preventive action, nonconformance management, supplier corrective action, calibration, validation, audit readiness, and other assigned Quality System processes. Analyzes quality and supplier performance data to identify trends, risks, and improvement opportunities and provides recommendations to leadership and Management Review. Leads and supports internal audits, supplier audits, regulatory inspections, notified body audits, and related readiness, response, and follow-up activities. Collaborates with Procurement, Manufacturing, Engineering, Research and Development, Regulatory Affairs, Supply Chain, Commercial, Quality Compliance, and other functions to improve products, processes, suppliers, and Quality Systems. Reviews and approves quality documentation, including Supplier Quality Agreements, procedures, work instructions, validation documents, inspection reports, and related records. Provides leadership, coaching, mentoring, and technical guidance to quality personnel and cross-functional partners. Communicates significant quality risks, issues, opportunities, and business impacts to management in a timely manner. Ensures compliance with Company Health, Safety, Environmental, regulatory, and quality requirements. Performs other duties as assigned. Experience and Knowledge: Bachelor's degree in Engineering, Science, Life Science, or a related technical field is required. Minimum 7 years of medical device industry experience is preferred, including responsibility for quality management