Senior Manufacturing Engineer

Job Type Full-time Description Sr. Manufacturing Engineer On-site | Full-Time | Permanent Salary 130,000-$155,000 We are not currently working with third party agencies on this role. About Us : Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do - and have a lot of fun doing it. About This Opportunity : We are seeking a process oriented and results-driven Sr. Manufacturing Engineer to lead process development and improvement in a medical device contract manufacturing environment at our San Jose, California site. The primary responsibility of this position is to apply high-level engineering principles to drive process improvements in the manufacturing of medical devices to positively affect Quality, Delivery, Cost, Safety and Morale. Additionally, this position will be responsible for executing large-scale projects while providing guidance and / or supervision to team members. We\'re looking for someone with a positive attitude and attention to detail who wants to grow professionally with high internal expectations. This role supports base business improvement and / or new product launches, develops tooling and fixtures, implements lean methodology, investigates issues using root cause analysis, implements improvements, manages CAPAs, and creates documentation such as standard work and validation protocols. The engineer collaborates cross-functionally to optimize designs for manufacturability and cost and communicates effectively with internal teams and customers. Key Responsibilities : Adheres to all safety and quality requirements including but not limited to : Quality Systems, U.S. Food and Drug Administration (FDA) regulations, company policies and operating procedures, and other regulatory requirements. Creates and implements lean processes in a cellular environment utilizing appropriate methods such as metals machining, sheet metal fabrication, and sub-processing such as assembly, powder coat, and metal finishing, welding, laser cutting, and electrical harness assembly. Performs root cause analysis to identify and implement needed process improvements eliminating waste Defines, produces and implements documents including standard work and process work instructions. Identifies, develops, justifies, and executes detailed project plans for engineering work with minimum supervision, which generates substantial improvements to the business Provides day-to-day guidance and / or supervision to team members Ability to lead new products launches effectively in a contract manufacturing environment. Investigates, develops and implements new process technologies. Successfully communicates complex issues with customers and internal team members. Creates, reviews and approves engineering drawings, equipment layouts, change orders and specifications. Develops tooling, fixtures and equipment used in manufacturing to optimize productivity and cost. Effectively owns and manages CAPAs pertaining to their areas of responsibility. Collaborates with development, programmers, machinists and suppliers to evaluate designs for manufacturability and cost reduction. Creates and executes validation protocols, processes and material evaluations. The successful candidate will : Plan and execute large scale projects, with minimum supervision, on time and within budget to achieve tangible results while providing daily guidance to assigned project resources Mentor and develop less experienced staff. Drive improvements through root cause analysis and data driven decision-making. Participates in cross-functional project teams to implement creative solutions. Ensure internal and external customer expectations are met or exceeded. Qualifications : Engineering or bachelor\'s degree in a technical field with applicable experience is required. Lean, SixSigma, and / or Project Management certification strongly preferred 15+ years of work experience in similar technical roles including medical device manufacturing required Strong problem-solving skills. Ability to provide solid rational and justification for process improvement change requests Lean manufacturing and new product development or launch support experience is highly desirable. Understanding of metals machining, sheet metal fabrication, processing, and polishing is strongly preferred. Ability to work in a team environment. Strong written and oral communication skills. Experience in medical devices is required. Proficiency in Microsoft Office Suite Working knowledge of ISO and FDA regulations and GD&T Working Conditions : Full-time on-site position Infrequent travel as needed for customer meetings and industry event

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