Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Sr. Engineer II to support various projects within Arthroplasty. This individual will be responsible for full life cycle development of medical devices, which includes initiation, design, development, execution, and product maintenance. The successful candidate would have a strong understanding of FDA and ISO guidelines for the development of medical devices. Additional preferred qualifications include knowledge of manufacturing processes, training in project management and communication skills, and a working knowledge of anatomy from an orthopedic standpoint, including joint anatomy. Proficiency in designing products using a 3D-CAD program is essential. The candidate should also possess technical expertise in development methodologies, design, and project implementation, along with familiarity with orthopedic surgery principles, theories, and products. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better.Essential Duties and ResponsibilitiesDesigns components or functional systems and modifies existing designs to develop or improve products and facilitate manufacturing operations.Recommends alterations to development and design to improve quality of products and/or procedures.Determines budgets and timelines for assigned projects.Leads multifunctional new product project teams, as assigned by Engineering Manager, through project technical feasibility analysis, initiation, planning, execution, and termination, adhering closely to project timeline and budget.Maintains design history file for assigned projects, adhering to Arthrex design control procedures.Provides Regulatory department technical support for assigned projects as needed.Supports Marketing and Product Management with technical information to be used for training and marketing of assigned products.Supports Manufacturing to provide processing improvements.Supports surgeon and distributor customers by training and/or educating on technical aspects of assigned products as needed.Determines necessity of testing and initiates testing of assigned products.Reports progress and status of assigned projects on a timely basis.May be required travel to attend trade shows and visit established accounts as well as prospective accounts.International travel may be required.SkillsKnowledgeable of FDA and ISO guidelines for the development of medical devices required.Manufacturing process knowledge preferred.Project management and communication skills training preferred.Working knowledge of anatomy from an orthopedic standpoint preferred.Working knowledge of joint anatomy preferred.Proficiency in designing products using a 3D-CAD program. Creo and/or SolidWorks experience preferable.Technical knowledge in development methodologies, design, and project implementation.Knowledge of orthopedic surgery principles, theories, and products preferred.Historical perspective on orthopedic surgery principals, theories, and products preferred.KnowledgeComplete understanding and application of principles, concepts, practices, and standards.Full knowledge of industry practices.Education/ ExperienceBachelors degree in Engineering required.8 years of relevant work experience required.Medical, Dental and Vision InsuranceCompany-Provided Life InsuranceVoluntary Life InsuranceFlexible Spending Account (FSA)Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)Matching 401(k) Retirement PlanAnnual BonusWellness Incentive ProgramFree Onsite Medical ClinicsFree Onsite LunchTuition Reimbursement ProgramTrip of a LifetimePaid Time OffEmployee Assistance Provider (EAP)All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.#J-18808-Ljbffr