We are looking to hire a hardworking Staff Quality Engineer to join our incredible team at Johnson & Johnson in Memphis, TN.
Growing your career as a Full Time Staff Quality Engineer is a great opportunity to develop relevant skills.
If you are strong in presentation, cooperation and have the right drive for the job, then apply for the position of Staff Quality Engineer at Johnson & Johnson today!
CrossRoads is recruiting for a Staff Quality Engineer , to be located in Memphis, TN . DePuy Synthes , part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit CrossRoads, recently acquired by DePuy Synthes , part of the Johnson & Johnson Medical Devices Companies, provides one of the most comprehensive orthopedics portfolios in the world. DePuy Synthes solutions, in specialties including joint reconstruction, trauma, craniomaxillofacial, spinal surgery and sports medicine, are designed to advance patient care while delivering clinical and economic value to health care systems worldwide. For more information, visit Are you ready to make an impact?
If you want to leave your personal mark and be valued for who you are, Johnson & Johnson offers an unusual experience to professionals looking for an opportunity to work with hardworking people who share your real passion for caring in an environment that empowers you to drive your own career and that you feel you can bring your whole self to work.
We are looking for someone to support the New Product Development Quality group to implement engineering and quality systems, and regulatory compliance strategies and objectives. As the Staff Quality Engineer you will get hands-on experience as part of a team to implement state-of-the-art quality engineering focus and improvements in design and development of products, and in transfer and steady state phases of manufacturing operations. Key responsibilities: Product development team member focused on product development and life cycle management activities related to the CrossRoads business. Lead design and development planning activities for new and sustaining projects. Participate in all aspects of the creation and execution of functional/design requirements for new and sustaining projects. Conduct formal technical design reviews throughout the phases of the product development process. Support and approve design verification/validation activities including mechanical testing, tolerance analyses, design rationales, and surgeon based anatomical labs. Apply statistical methods and design excellence tools to design verification and validation activities. Support risk management activities including planning, design & clinical risk management, production risk management, and overall risk summary reporting. Support transfer to manufacturing activities both in product development and base businesses. Enhance the design control and risk management processes to better reflect state of the art practices and drive continuous improvement. Provide leadership in all areas of the Quality System, including, but not limited to corrective & preventive actions, product complaints, post market surveillance, nonconforming materials, risk management, and audit support functions. Provide leadership in the understanding of medical device regulations to other disciplines. Communicate effectively at all levels within Quality, as well as cross functionally with departments such as Product Development, Regulatory, Manufacturing, and Marketing. Work closely with suppliers on the qualification of new/changed parts and processes supporting product development. This person will conduct assessments of new suppliers as part of the project teams. Know and follow all laws and policies that apply to one's job, and maintain the highest levels of professionalism, ethics , and compliance at all times. Diligently participate in our compliance program-related activities as denoted by your supervisor or our Chief Compliance Officer. Additional duties as assigned. Education
Bachelor's degree in Engineering and/or in a Technical Science is required. A Master's degree is a plus. Experience A minimum of 6 years of related working experience in a GMP and/or ISO regulated industry Strong design/quality engineering skills with a proven track - record in all aspects of the design control process, including functional/design requirements, design verification/validation, and product risk management Strong working knowledge of QSR (21 CFR 820) and ISO (13485, 14971) quality requirements Candidate should possess excellent problem solving, decision-making, and root cause analysis skills in addition to people skills that foster conflict resolution as it relates to technical situations Candidate should have a proven track-record implementing Quality System improvements to meet compliance and overall business goals. Proficiency with the Microsoft Office Suite Must be able to travel up to 20%, including possible global travel Blueprint literacy including GD&T Knowledge of process and design excellence tools is strongly preferred; Certification is a plus Working knowledge related to orthopedic implantable, product software, and software validation Strong working knowledge of Analytical Tools and Advanced Statistical Analysis Other: Six Sigma/Process or Design Excellence training, and/or certification Ready to be part of something great? Don't forget to apply. We want YOU!
At Johnson & Johnson, we're on a mission to change the trajectory of health for humanity. That starts by creating the world's healthiest workforce. Through cutting-edge programs and policies, we empower the physical, mental, emotional and financial health of our employees and the ones they love. As such, candidates offered employment must show proof of COVID-19 vaccination or secure an approved accommodation prior to the commencement of employment to support the well-being of our employees, their families and the communities in which we live and work.
For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit .
Johnson & Johnson is an Affirmative Action and 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, or protected veteran status and will not be discriminated against on the basis of disability.
Benefits of working as a Staff Quality Engineer in Memphis, TN:
? Company offers great benefits
? Company offers career progression opportunities
? Attractive package
