Date Posted
Tustin, CA
Salary Range
$65,000.00 - $70,000.00
Job Duties and Responsibilities
  • Collect and summarize the customer’s needs. Develop/provide the concept samples to customer by using existing Company techniques and new techniques as needed.
  • Prepare the drawing or specification documents as a deliverability of concept freeze.
  • Contribute to the collection of the latest processing technologies/medical techniques information.
  • Provide technical support communication between Company Group’s and US customer.
  • Design, run, and gather data for experiments. Participates in the design of prototypes, new test methods and processing procedures.
  • Significantly self-directed. Determines and pursue courses of action necessary to obtain desired results (recommendation of assignments is often self-initiated).
  • Apply technical principles, theories, and concepts for developing new treatment approaches and concepts towards the solution of complex technical problems and provides solutions which are innovative and ingenious.
  • May be responsible for planning, developing, coordinating, and directing engineering development or a number of small projects with many complex features, utilizing internal and external resources.
  • Ensures appropriate communication processes and tools are established within and across functional groups.
  • Contributes to product transfer and scale-up activities, assembles technical documents and conducts training to sister plant’s technical staff.
  • Manage direct or in-direct reports as required.
  • Maintain R&D laboratory to facilitate efficient prototype and process development.
  • Coordinate effectively with Company Group’s other sites.
  • Other general office duties as required.
Required Experience
  • Bachelor’s degree or higher in an engineering field.
  • Good analytical, critical thinking, innovative thinking and problem solving skills.
  • Productive team player.
  • Sense of urgency, able to multitask, prioritize activities, manage risks, and complete tasks on time.
  • Excellent oral and written communication along with good presentation and technical writing skills.
  • Must be fluent in Japanese and English (speaking, reading and writing), business
  • Ability to create a drawing in software such as AutoCAD or SolidWorks.
  • Functional familiarity with the FDA submission process, ISO requirements, and QSR requirements is also preferred.
  • Requires the ability to travel approximately 5% of the time throughout the United States and internationally.