Johnson & Johnson is currently seeking an Senior Source Quality Engineer (m/f/d) to join our team located in Norderstedt, Germany. 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 https://www.jnj.com/. Position summary The Senior Source Quality Engineer (Sr. SQE) provides overall quality assurance leadership in the management of Direct, Indirect Suppliers and/or External Manufacturers engaged in the production of Johnson and Johnson products. He/she leads the deployment of the Source Quality Management (SQM) strategies and associated standards, policies, procedures, programs, systems, processes, and initiatives for Ethicon Supply Chain Suppliers. Duties & Responsibilities In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position: Provide timely business support for the assigned Ethicon Source Quality Management (SQM) function globally. Lead, develop, and implement supplier/purchasing controls and associated activities including Approved Supplier List management. Participate in and/or support the identification, selection, qualification, monitoring, and disengagement of suppliers for Source Quality Management. May lead this process under the guidance of Source Quality Manager and/or management representative. Collaborate with suppliers and business partners to ensure robust materials, products, processes, and systems. Partner with Procurement, R&D, Engineering/Technical Operations, Quality, Operations, and Suppliers in the timely investigation, resolution/prevention of supplier-related issues to minimize/prevent business disruptions. Monitor and analyze supplier performance metrics, identify areas of opportunity, communicate supplier risks, and drive the resolution of supplier quality issues and risk control processes. Implement supplier change management process including change notification, dissemination of information, impact assessment, approval of changes, and supports material/supplier qualifications. Own, drive, and lead the assigned Source Quality related projects, activities, initiatives with limited supervision. Utilize Project Management methodologies to plan, organize, connect, shape, lead, and deliver results for SQM projects. Utilize analytical and problem-solving skills to develop and optimize supplier performance. Analyze quality data and identify trends impacting risk benefits requirements of product and quality systems for external suppliers. Actively participates in discussions to drive resolution. Collaborate with operations and franchise operations development on process/product improvement projects. Prepare Supplier Quality Agreements and drives discussion with supplier while consulting Source Quality Manager and/or management representative. Develop/execute Quality Risk Management process for supplier-related matters with partnerships of subject-matter experts Own and lead the Source Quality Relationship Management (SQRM) process for the assigned suppliers (e.g. Lead periodic SQRM meetings including supplier quality performance reviews, supplier investigation follow-ups, investigation responsiveness/cycle time, targeted improvement plans (TIP), closed loop corrective actions, NC reductions, supplier quality metrics, etc.). Understand or anticipate the customer's needs and adds value by providing specific metric information tailored to the particular business environment. Take actions to identify internal customer requirements and translate customer requirements into potential proactive improvements to components or supplier quality systems. Proactively pursue clarification to confirm understanding of internal customer needs and requirements. Follow up on commitments and keeps customer, management and appropriate parties apprised. Respond proactively to changing regulatory and business needs. Lead component qualification change projects in collaboration with key business partners and the supplier's applicable functional groups. Apply appropriate Quality Engineering and PEx tools (e.g. PM/VSM, Kaizen, DMAIC, FMEA/FTA, RCA, MSA, SPC, Cp/Cpk/Cpm/Ppk, Hypothesis Testing, ANOVA/DOE/EVOP, etc.) to support innovations and continuous improvements. Comply with all applicable quality management system, environmental, safety and occupational health policies. (for example, ISO 13485, ISO14001 & OSHAS18001). Responsible for communicating business related issues or opportunities to next management level. For those who supervise or manage a staff, 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 applicable Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures. Performs other duties assigned as needed. Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable. Experience & Education A minimum of a Bachelor's degree in Engineering, an Applied Science or a related technical and quality field is required. A minimum of 4 years of experience in a highly regulated industry is required. Prior manufacturing, plant or technical background is required. Working experience in good manufacturing practice regulated environment is preferred (medical device, pharmaceutical, etc.). Demonstrated knowledge of manufacturing principles and practices, and procedures. Direct experience in plant and/or supplier GMP auditing is preferred. Broad experience with quality systems, including but not limited to validation, non-conformance, CAPA systems and investigations, laboratory controls, production and process controls, is required. Experience with documentation and technical writing skills, in a regulated compliance environment, is required. Component Qualification/Process Validation experience is preferred. New product introduction experience is desired. Prior experience with FDA inspections is desirable. Broad knowledge of Quality System Regulations and Source Quality Management principles are desired. Demonstrated ability to identify compliance risks and assess business impact, is required. Ability to manage complexity and work in a diverse team environment is essential. Ability to deal with complex issues using deductive reasoning, critical analysis skills and systematic approaches. Required knowledge, skills and abilities Working knowledge of regulatory compliance requirements (i.e. Quality System Regulations (QSRs), Medical Device Directive (MDD), ISO 9001, ISO 13485, ISO 14971 or other international standards) required. Working knowledge of Quality issue investigation, Non-Conformance Reports (NCRs), Corrective and Preventative Actions (CAPAs) preferred. ASQ Certifications for Certified Quality Engineer (CQE), Quality Manager (CQM), and/or Supplier Quality Professional (CSQP) preferred. Quality Auditor qualifications or Lead Auditor certifications such as ASQ Certified Quality Auditor (CQA) or Biomedical Auditor (CBA) preferred. Flawless Project Execution (FPX) or Project Management Professional (PMP) trained and certified preferred. Six Sigma Black Belt/ Green Belt (CSSBB)/CSSGB) or Lean certification from a recognized program or PE leadership training preferred Strong analytical skills, metrics development and ability to identify trends are desirable. Knowledge of specific business practices and software applications skills (Word®, Excel®, PowerPoint®, Minitab®, Visio®, Microsoft Project®) is preferred Must have strong business acumen. The ability to collaborate with all levels of management in cross-functional team environment is required. Ability to communicate effectively in English. Bilingual in English and other language (Spanish, German, Portuguese, or Mandarin) is preferred. Additional position requirements Personal protective equipment such as: Ear plugs, Safety Glasses, and Safety shoes. Ability to work in stressful/fast paced environment. Ability to work and interact with co-workers to accomplish company goals in a team environment. Management Skills. Analytical/Problem Solving Skills. Ability to communicate verbally and in writing. Ability to learn. This position may require up to 25% domestic and international travel. Responsibility for others & Internal interactions This position reports to Source Quality Manager, Sr. Manager Source Quality Supervisor. This position works closely with Procurement/Strategic Sourcing, Engineering/Technical Operations, plant associates and Quality Compliance. What we offer Our employees are just as important to us as our customers. At Johnson & Johnson, we like to think long-term and enable successful careers with interesting career paths within our company. We do everything we can to enable you to develop your full potential with us. We are very proud of our open, appreciative corporate culture and value a healthy balance between work, family and leisure. Flexible working time models such as part-time, flexible time and home office can be adapted to your life. Our proactive health program supports your mental and physical well-being. Working at Johnson & Johnson For more than 130 years, diversity, equity & inclusion (DEI) have been part of our cultural fabric at Johnson & Johnson and woven into how we do business every day. Our commitment to respect the dignity and diversity of all is embedded in our Credo. We know that the success of our business depends on having the best talent in a workforce that reflects the diverse markets we serve around the world and an inclusive culture that values different perspectives and life experiences. That is why we are working to create an inclusive environment where diverse backgrounds, perspectives and experiences are valued and each and every one of our people feels that they belong and can reach their potential. No matter who they are. Johnson & Johnson Family of Companies are equal opportunity employers, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law. A cover letter is not required for your application, but we kindly ask that you include a brief statement explaining why you are applying in your resume or CV. To ensure a fair recruitment process, please refrain from adding a photo in your CV.