Mechanical Engineer V

Job Title: Mechanical Engineer VWork Site: Pleasanton, CA 94588 – OnsiteDuration: 12 Months Contract with possible extensionShift/Schedule: 8:00 AM – 5:00 PM/M-FPay Rate/Range: $60.00-$65.00/hr on W-2 through Select Source International Job Responsibilities:Performs complex activities in the testing and sustaining of class II and class III mechanical circulatory support products including Ventricular Assist Devices (VADs), extracorporeal blood pumps, and oxygenators. Provides technical solutions to a wide range of difficult problems. Exercises considerable latitude in determining technical objectives and solutions of assignments. Responsibilities:Research, test, and sustain electromechanical devices for VAD applicationsWork with cross-functional teams for development of new products, and improvement to existing products driven by corrective and preventative actions (CAPA)Use experimental, empirical, and numerical analysis to evaluate designs.Develop and qualify (IQ/OQ) fixtures/equipment for verification testingInvestigate issues and identify root causes in complex systems where analysis of situations or data requires an in-depth evaluation of various factorsIdentify and mitigate technical risksCreate/review technical drawings for appropriate assembly, dimensioning, and tolerancingKnowledgeable in GD&TAble to review/create tolerance analysis of existing systemsUnderstands complex machined parts, injection molded parts, extrusions, molding of siliconeWide range of assembly techniques (laser welding, ultrasonic welding, bonding, mechanical joining)Experience with risk management FMEA’sAid in vendor evaluations such as manufacturing capability and capacity, engineering support, and quality controlsComplies with FDA regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendorsSupport all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Minimum Qualifications:B.S. in Mechanical, Biomedical, or Manufacturing Engineering.8 years engineering experience including product development, process development, risk assessment, and V&V verification related to class II/III medical devicesIndustry experience with FDA design controls 21 CFR 820.30Strong communication and presentation skills (e.g. versatility communicating with peers, management, auditors/regulators, and customers)Ability to travel approximately 10%, primarily in the US, but may include international) Preferred Qualifications:Design and V&V of class II/III electromechanical medical devices, such as VADs, extracorporeal blood pumps, oxygenators, or other implantable devicesExperience with medium to high volume medical device manufacturingExperience with a variety of manufacturing processes and designing for manufacturability Industry experience with EU MDR, ISO 13485, and standards for medical devices (e.g. biocompatibility, sterilization, labeling, packaging, etc.)Experience with CAD design, SPC/six sigma, DOE, and project managementCompany DescriptionSelect Source International (SSI) is a distinguished staffing company with nearly 25 years of experience, renowned for delivering top-tier workforce solutions encompassing staffing, recruiting, and managed services. As a proud supplier, we bring a wealth of expertise and best-in-business differentiators to comprehensively support your diverse workforce needs.Based in Minneapolis, Minnesota, USA, SSI has established itself as a global leader, serving a broad clientele across industries with unwavering dedication and excellence. SSI is ISO 9001, 14001, and Soc2 Type2 certified, underscoring our commitment to quality and security. We have garnered numerous sustainability and supplier diversity awards, further validating our industry-leading capabilities

Salary : $60 - $65