Quality Engineering Manager

The Manager, Manufacturing Quality Engineering (QE) is responsible for managing all aspects of Operations Quality Engineering functions within the value stream(s) of Access, Closure and Peripheral to which they are assigned. They must also ensure overall uniformity in QE operating norms and execution by coordinating and aligning with other QE management. Additionally, they are responsible for ensuring compliance with the applicable regulations of all countries in which Terumo Medical either manufactures or distributes products including, but not limited to the U.S. Quality System Regulation, Japanese Pharmaceutical Affairs Laws, the Canadian Quality System Regulation, and the Medical Device Directive.Manage a team of Quality Engineers in driving robust problem solving, NC reduction and continuous improvement efforts. Drive value stream optimization through the application of proven methodologies such as Six Sigma, LEAN, Kaizen events etc.Manage all aspects of Operations QE within their VS, including:Daily production support (Nonconformance investigations, product dispositioning, yield monitoring)Organizational and Corporate quality initiativesProject supportCooperatively and effectively partner with Value Stream Leaders, Operations Managers and Supervisors to develop and implement strategies which promote the Terumo Quality Culture throughout operationsProactively manage the workload and deployment of their team to ensure support of the business by evaluating resource supply vs. demand and ensuring an appropriate organizational structure and skillset/experience mix is createdEstablish and promote a work environment that supports compliance with the TMC Quality System and Terumo's policiesOwn and maintain Process FMEA assessment and documentationEnsure appropriate process control plans (SPC, sampling, inspection methods) are created, maintained and are effectiveManage operations-related CAPA activities in a complete and timely mannerEnsure transfers to manufacturing are data driven and robustly executedPrepare for and support compliance audit activities in OperationsMaintain Quality Performance Indicators in support of management oversight activitiesSupport the preparation and conduct of compliance forums such as Quality System Management Reviews, Change Board Meetings, NC/CAPA Board meetings etc.Promote the professional growth and development of QE associatesPerforms other job related duties assignedPosition RequirementsKnowledge, Skills and Abilities (KSAs)Knowledge of national and international regulations applicable to medical devices including; Quality System Regulations, 21 CFR 820, 21CFR 803 and 804 (MDR regulations), Canadian Medical Device Regulations, ISO 14971, ISO 13485, and MDR etc., LEANAbility to identify and help establish the strategic direction of the quality assurance systemAbility to analyze and interpret all regulatory and quality guidelines as neededDemonstrate a strong understanding and working knowledge of the Quality Sciences (Acceptance Sampling, SPC, continual improvement, Six Sigma, LEAN, Design of Experiments, COQ, Cause & Effect analysis etc.)Demonstrate a strong “business partner” approach and attitude providing creative and innovative solutions that meet quality standardsData analysis via Excel and other statistical software (Minitab, JMP, PowerBI)Must be proficient in Microsoft Excel, Word, PowerPoint, and OutlookBachelor's degree in engineering, science, or math requiredMinimum of 7 years Quality Assurance experienceMinimum 3 years Quality management experienceExperience in medical device manufacturing environment coupled with certifications from ASQ preferredEmployee Value PropositionWe believe that the future is bright for everyone at Terumo. We work with the future in mind to generate lasting change, create a bigger impact and produce greater outcomes for today, and for decades to come.At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat – progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, sustainable solutions for patients.Join us, and help shape wherever we go next!Advancing healthcare with heartWe provide competitive and comprehensive benefit options that allow you to design your own plan based on your individual needs which include: paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD'D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program. Inal compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. Range is $107,000 - $140,000#J-18808-Ljbffr