Sr Supplier 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 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 Supply Chain Engineering Job Sub Function Quality Engineering Job Category Scientific/Technology All Job Posting Locations: Palm Beach Gardens, Florida, United States of America Job Description Job Description: DePuy Synthes, a member of Johnson & Johnson's Family of Companies, is recruiting for a Sr. Supplier Quality Engineer to be located in Palm Beach Gardens, FL. 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. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech The Sr. Supplier Quality Engineer provides overall quality assurance leadership in the management of select contract manufacturing sites and raw material suppliers engaged in the production of DePuy Synthes products. Works collaboratively with management to drive decisions regarding Quality Engineering methods to produce leading-edge customer-tailored engineering final deliverables. Key Responsibilities Implement SQ strategy and follow Supplier Quality standardsManage supplier related Non-Conformities (NC/ SCAR) and Corrective and Preventive Actions (CAPA)Oversee supplier change requests (SCR)Support Process Validations at suppliersSupport QE with supplier product PVE's (First Article Inspection, Control Plans, Critical to Quality, Capability studies)Contribute to product investigations related to product and process complaints.Provide Supplier Quality Engineering support for PLM changes.Support supplier preparation for inspections by authorities / third partiesSupport Procurement executing supplier transfer projectsSupport for Quality Agreement and Change Agreements, supplier assessments and supplier audit processReport on supplier performance metrics and management reviews.Lead or participate in Quality projects: Legacy review, remediation, integrationImplementation of improved/new standards for supplier qualityResponsible for communicating business-related issues or opportunities to next management levelResponsible for following all company guidelines related to Health, Safety and Environmental practices as applicable.Responsible for ensuring that subordinates follow all company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicableResponsible for ensuring personal and company compliance with all Federal, State, local and Company regulations, policies, and proceduresMay directly or indirectly supervise and/or provide directions to other Supplier Quality Engineers.Collaborate with other functional departments such as Quality, Engineering, R&D, Regulatory and SourcingMay interact with government agencies such as the FDA, Regulatory Agencies such as Notified Bodies and will interact with suppliers providing products and services that could impact the quality of J&J productsPerforms other duties assigned as needed Qualifications Education: Bachelor's or equivalent university degree is required; A concentration in Engineering, Life Science, or related field is preferred Required Experience and Skills: A minimum of 2-4 years of experience in a GMP and/or ISO regulated industryStrong communication, teamwork, and problem-solving skillsStrong root cause analysis skillsAbility to work in stressful/fast-paced environmentAbility to work and interact with co-workers to accomplish company goals in a team environmentAnalytical/Problem Solving SkillsAbility to communicate verbally and in writingAbility to learn Preferred Experience in the medical device and/or pharmaceutical industryFDA and ISO regulations knowledgeExperience or knowledge with machining manufacturing processes, injection molding, robotics, electronics and/or softwareOperations supplier quality experienceFDA CFR Part 820 and/or ISO 13485 knowledgeAuditing backgroundManagement skills Other Fluency (oral & written) in English is requiredUp to 10% travel may be requiredSix Sigma, Lean, or ASQ Certification and professional licenses preferred 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 https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource. Required Skills Preferred Skills: Analytical Reasoning, Coaching, Customer Centricity, Data Savvy, Document Management, Financial Competence, Good Automated Manufacturing Practice (GAMP), Lean Supply Chain Management, Process Improvements, Quality Control Testing, Quality Services, Quality Standards, Quality Systems Documentation, Quality Validation, Science, Technology, Engineering, and Math (STEM) Application, Supervision, Supply Planning, Technologically Savvy The anticipated base pay range for this position is : $79,000.00 - $127,650.00 Additional Description For Pay Transparency This position is eligible to participate in the Company’s long-term incentive program. Benefits 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