Manufacturing Engineer, I

Job Title: Manufacturing Engineer, I

Location: Stockton, CA

Employment Type: Full-Time / Exempt

Supervisor: Engineering Manager

About Us:

Vantedge Medical is the premier metals-based digital solution and power generation infrastructure 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 the power generation and data-center industry with precision forming and automation. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top alternative energy producers and data storage providers around the globe. With a steadfast commitment to Making a difference in the advancement and direction of power, data, and digital infrastructure drives us to go above and beyond every day. We take immense pride in the work we do – and have a lot of fun doing it.

About the Role:

We are seeking a results-driven Manufacturing Engineer to be responsible for supporting the growth and continued success of our manufacturing plant in Stockton, CA. Working with the direction of management and senior coworkers in the plant, the primary duties of this position are to apply engineering principles to solve technical problems, create the appropriate documentation in support of successful product launches, and improve overall Quality, Delivery, Cost, and Safety performance metrics. 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, I expected to communicate effectively with customers as well as internal stakeholders.

 

Responsibilities:

• Create a safe working environment through adherence to site safety requirements for yourself, coworkers and visitors and a willingness to raise awareness on unsafe practices
• Develop and implement manufacturing processes in a lean production environment that support 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 assigned launch readiness and NPI deliverables associated manufacturing and production such as line balance, process design, pFMEA, etc. at the direction of the project engineer or project manager
• Execute technical manufacturing engineering processes including but not limited to MRB, CAPA, ECO approval & implementation, root cause analysis and effective corrective action countermeasure, deviation authorization, training, etc.
• Produce and implement manufacturing documents including drawings, production routings, standard work, method sheets, and process work instructions.
• Develop tooling, fixtures and equipment used in manufacturing to optimize productivity and cost
• Communicate and provide technical perspectives on complex issues with internal stakeholders both face-to-face on site and remotely (e.g., TEAMS).
• Investigate, develop, justify and implement new process technologies to reduce costs.
• Adhere to all site Quality Management System (based on ISO-9001), governing agency regulatory, and customer-specified requirements and guidelines

Requirements / Skills:

• Bachelor’s Degree in an engineering or equivalent technical field. 
• Up to 3 years of work experience in a similar technical role(s). 
• Problem-solving skills and a go-to toolbox of techniques.
• Ability to provide solid rationale and justification for process improvement changes. 
• Working level of Lean Manufacturing knowledge and implementation.
• New Product Introduction experience preferred. 
• Understanding of metals fabrication, preferably sheet metal fabrication, processing (weld and finishing), and inspection.
• Ability to work and collaborate in a team environment. 
• Ability to apply and interpret GD&T.
• Strong written, presentation, and oral communication skills.
• Experience in medical device manufacturing as a Contract Manufacturer.
• Proficiency in Microsoft Office Suite.
• Working knowledge of ISO and FDA regulations.