Quality Engineer II Job

Job description

Quality Engineer II-7875151028DescriptionMentor Worldwide L.L.C., a member of the Johnson & Johnson family of companies, is recruiting for a Quality Engineer II for its location in Irving, TX.Mentor Worldwide L.L.C is a trusted global leader in aesthetic medicine among both consumers and clinicians by providing a broad range of innovative, science and clinical-based solutions to maintain, enhance, and restore self-esteem and quality of life. The company has products and services in three areas of aesthetics: breast (augmentation and reconstruction), body and face.
Use Quality Engineering principles, tools and techniques to develop, and optimize, and support systems and processes that are aligned with the overall Company strategy and mission affecting continuous quality improvement.
Responsibilities:Support, consult, train and lead quality improvement projects throughout the life cycle of Mentor products, including product design and development, manufacturing, purchasing, and improvements. Utilize quality Engineering tools and techniques to establish sampling plans, develop quality plans, conduct and participate in FMEA activities, support reliability engineering activities, conduct process and systems audits and to assist in specification development. Analyzes routine and test data looking for improvement opportunities. Designs and implements experiments (DOE's) for process and product improvement and validation testing. Provides statistical support for sampling plan and analysis, DOEs, Paretos, ANOVA, and SPC applications. Evaluate manufacturing quality performance capability and develop criteria to monitor and improve existing processes. Investigation of nonconforming material and assist with the determination of root cause, corrective action and recommendation of disposition for the Material Review Board (MRB). Develop personal performance objectives based upon the facility quality objectives, reporting monthly on progress made against those goals. Perform Internal Audits to ensure compliance with QSR, 21 CFR Part 820, ISO 13485, MDD and Canadian Regulation in accordance with the Internal Audit schedule. Provide QE support to meet QAC objectives at the Mentor TX and Mentor Byron Medical (Body Contouring) Product Lines.
QualificationsA Bachelor’s degree (B.S.) in engineering, science, mathematics or statics is required. A minimum two years manufacturing related experience and/or training; or equivalent combination of education and experience is required. Experience in medical device manufacturing is preferred. The ability to prioritize and manage multiple projects with no negative impacts to the business, in addition to time management skills is required. Strong communication, teamwork, and problem solving skills are required. Six Sigma, Lean, or ASQ Certification and trainings are preferred. This position will be based in Irving, Texas and will require up to 10% domestic travel.
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J2W: LI NAPrimary Location:North America-United States-Texas-IrvingOrganization: Mentor Texas LP (6182)Job Function: Quality (Eng)Certain sites within the Johnson & Johnson Family of Companies participate in E-Verify as appropriate in accordance with Company guidelines and federal or state law. To learn more about the government sponsored program and to see a list of the sites that are currently enrolled, please click here.
Johnson and 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. EEO is the Law EEO is the Law GINA Supplement