Manufacturing Engineer II

Manufacturing Engineer II

Full-time | Permanent

Salaried | On-Site

$110k - $120k

We are not currently working with third party agencies on this role.

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.

We are seeking a process-oriented and results-driven Manufacturing Engineer to take the technical lead in process development, new product launches, and overall improvements in a medical device and data center industry contract manufacturing environment at our San Jose, California site. The primary responsibilities of this position are to apply engineering principles to drive activities that lead to successful product launches and improve overall Quality, Delivery, Cost, Safety and Morale.

We’re looking for someone with a positive attitude and attention to detail who wants to grow professionally with high internal expectations. In this role, the Manufacturing Engineer is required to communicate effectively with customers as well as internal stakeholders.

• Create and implement lean processes in a cellular environment that incorporate machining, sheet metal fabrication, and electro-mechanical assembly with associated sub- and outside-processing (e.g., powder coat, metal finishing, welding, laser cutting, and electrical harness assembly).
• Complete launch readiness NPI deliverables associated within a manufacturing environment (i.e., design transfer).
• Lead process improvement projects at the technical level including analyzing the data, creation of the problem statement, executing methodology, and outlining the benefits.
• Execute technical manufacturing activities including but not limited to MRB, CAPA, ECO approval & implementation, root cause analysis and effective corrective action countermeasure, deviation authorization, training, etc.
• Define, produce and implement manufacturing documents including routings, standard work, method sheets, and process work instructions.
• Develop tooling, fixtures and equipment used in manufacturing to optimize productivity and cost.
• Create and execute validation protocols, processes and material evaluations.
• Communicate and provide influence over complex issues with customers and internal stakeholders both face-to-face on site and remotely (e.g., TEAMS).
• Investigate, develop, justify and implement new process technologies to reduce costs.
• Collaborate with development, programmers, machinists and suppliers to evaluate designs for manufacturability and cost reduction.
• Adhere to all safety and quality requirements including but not limited to:
  Quality Systems, U.S. Food and Drug Administration (FDA) regulations, ISO, company policies and operating procedures, and other regulatory requirements.
• Infrequent travel as needed for customer meetings and industry events (