Sr. Engineer - Disposables R&D, Sustaining
Location: Minneapolis, MN, United States
Job Title: Sr. Engineer - Disposables R&D, Sustaining Location: Plymouth MN Duration:12 Months Supports design and development of product changes, within sustaining engineering, for disposable medical devices. Essential Duties and Responsibilities: This section contains a list of primary responsibilities of this role that account for 5% or more of the work. The incumbent will perform other duties assigned. * Lead and support small to medium sized projects with global cross-functional teams in the implementation of design changes (e.g. new features, suppliers, materials, labeling, CAPA/NCR, cost reduction, remediation). * Identify, investigate, and solve engineering problems utilizing risk-based and customer focused approaches and engineering tools. (e.g. dFMEA, Human Factors Engineering, statistical software, CAD). * Create, modify, and maintain design history file documentation including protocols, reports, design specifications, labeling, and design drawings. * Develop and execute test method validations, product testing, and verification / validation activities. * Build prototypes and models. May operate machine tools, design and build basic tooling, test fixtures and assembly equipment. * Adhere to design control procedures, general safety rules, company policies and procedures, FDA and international regulations and guidance. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. List knowledge, skills, and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform essential functions. * Working knowledge of plastics materials and processing such as injection molding, extrusion, ultrasonic welding, UV/solvent bonding, and sterilization. * Working knowledge of CAD and PDM enterprise software (e.g. Creo, Solidworks). * Working knowledge of FDA Design Controls and ISO 13485 Quality Management Systems. * Working knowledge of ANSI/AAMI/ISO 14971 Medical Devices - Application of Risk Management to Medical Devices. * Takes initiative with a high aptitude for learning, innovation, and implementing best practices and continuous improvements. * Strong collaboration, verbal and written communication skills. * Strong attention to detail, organized, and able to independently manage multiple priorities. * Ability to read, write and comprehend English. Experience and/or Background BS in Mechanical, Plastics, Biomedical Engineering or a related field, MS preferred. * 3 - 5 years of related experience in Class II or Class III disposables medical product development. * Design for Six Sigma (DFSS) training or certification preferred.
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