Metrology Technician

Job TitleTasks and ResponsibilitiesAssist Engineers with tasks related to measurement method development and support in compliance with quality regulations for medical device manufacturing.Setup and conduct test method validation for variable and attribute test method validation activities, including sample creation, developing test method work instructions.In coordination with site the quality team, calibrate measurement instruments and equipment at regular intervals, and perform preventative maintenance when applicable.Develop robust measurement systems per medical device requirements, program CMM and automated vision systems, develop test methods for hand tools and gages.Review, interpret, and analyze Geometric Dimensional and Tolerance (GD&T) requirements per specifications to perform test method development and validation.Interpret specifications, drawings, customer documentation and other documents as necessary to support metrology projects.Plan, coordinate, conduct Test Method Development and Validation activities, Initiate inspection plans for new/revised product.Perform measurement system analysis (MSA) for Gage 1, Gage Repeatability and Reproducibility (GRR), Bias and Linearity, Resolution studies.Perform statistical analysis of inspection data, process characterization, DOE results, ANOVA, Capability Analysis.Support Engineering and Supplier Quality group in identification of equipment and/or calibration providers.Support Engineering, Manufacturing, and Inspection personnel in design, methods, tooling, validations, and other areas related to the control of product.Support other quality activities as necessary such as customer complaint (CC) and RMA system per procedures, corrective and preventive actions (CAPA).Support internal and external audits.Education and ExperienceRequired:2 year degree in quality, manufacturing, engineering, or related equivalent experienceRegulated manufacturing industry experienceDesired:2+ years of regulated manufacturing experience.Quality certification(s) (e.g. ASQ CQE, CQT, CQA, etc.).Class I, II and/or III Medical Device manufacturing experience.Knowledge and experience with GMP/ISO Standards.CompetenciesAbility to read, write, speak and understand the English language (with a help of a translator, if needed)Ability to communicate clearly by conveying and receiving ideas, information and direction effectivelyAbility to demonstrate adequate job knowledge to deliver a world class performanceAbility to challenge oneself to consistently meet all goals and deadlinesWillingness to strive for excellence by producing work that is free of errors and mistakesDesire to delight both customers and coworkers by offering encouragement, fostering teamwork and addressing conflict appropriatelyCommitment to making improvements company wideDemonstrated competence using Microsoft Office, Project, Access and JMPComprehensive understanding of applicable Work Instructions, SOP'S, and ISO standardsWorking knowledge of statistical methods associated with six sigma and quality control.Able to perform math functionsEffective project leaderExperience with lean manufacturing principles and their implementationGood hand/eye coordination and depth perceptionGood manual dexterityCorrectable normal reading distance vision#TMSEqual Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.