About the role
Description Manufacturing Engineer II Job Type Full-time Stockton, CA Manufacturing Engineer II Onsite | Full-Time | Permanent Salaried| $85K - $128K *We are not currently working with third party agencies on this role. About Us: Vander-Bend is a U.S.-based manufacturer dedicated to building the precision infrastructure that powers tomorrow’s AI. Our expertise in server racking and power delivery solutions provides the backbone for next-generation data centers, enabling hyperscalers and integrators to innovate and scale globally. With a focus on trusted, domestic manufacturing, we deliver quality, speed, and innovation at scale—redefining AI infrastructure for the future. We are a newly created division of Vantedge Medical, the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. With a steadfast commitment to advancing technology, we take immense pride in the work we do – and have a lot of fun doing it.
Vantedge Medical™ is seeking a process-oriented, results-driven Manufacturing Engineer II to lead process development and improvement within our medical device and data center contract manufacturing environment at our Stockton, California site. This role applies engineering principles to drive manufacturing process improvements that positively affect quality, delivery, cost, safety, and morale. We're looking for someone with a positive attitude, sharp attention to detail, and high internal standards who wants to grow professionally.
This role supports base business improvement and new product launches, develops tooling and fixtures, implements lean methodology, investigates issues through root cause analysis, 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 Quality Systems, FDA regulations, ISO standards, company policies and procedures, and other applicable regulatory requirements
Creates and implements lean processes in a cellular environment using methods such as metals machining, sheet metal fabrication, and sub-processes including assembly, powder coat, metal finishing, welding, laser cutting, and electrical harness assembly
Performs root cause analysis to identify and implement process improvements that eliminate waste
Defines, produces, and implements documentation, including standard work and process work instructions
Identifies, develops, justifies, and executes detailed project plans with minimal supervision
Launches new products effectively in a contract manufacturing environment
Investigates, develops, and implements new process technologies
Communicates complex issues clearly with customers and internal team members
Creates, reviews, and approves engineering drawings, equipment layouts, change orders, and specifications
Develops tooling, fixtures, and equipment to optimize manufacturing productivity and cost
Owns and manages CAPAs within their area 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
What You'll Bring
Ability to plan and execute projects with minimal supervision, on time and within budget, to deliver tangible results
A track record of driving improvement through root cause analysis and data-driven decision-making
Strength participating in cross-functional project teams to implement creative solutions
A commitment to meeting or exceeding internal and external customer expectations
Requirements
Bachelor's degree in Engineering or a related technical field
5+ years of experience in similar technical roles, including medical device manufacturing, required
Strong problem-solving skills
Ability to provide sound rationale and justification for process improvement change requests
Lean manufacturing and new product development or launch support experience highly desirable
Understanding of sheet metal fabrication, processing, and polishing strongly preferred
Ability to work effectively in a team environment
Strong written and oral communication skills
Experience in medical devices preferred
Proficiency in Microsoft Office Suite
Working knowledge of ISO and FDA regulations, and GD&T