JOB RESPONSIBILITIES
• Evaluates manufacturing processes by designing and conducting research programs; applying knowledge of product design, fabrication, assembly, tooling, and materials; conferring with equipment vendors; soliciting observations from operators.
• Improves manufacturing efficiency by analyzing and planning work flow, space requirements, and equipment layout.
• Completes design and development projects by training and guiding technicians.
• Develops manufacturing processes by studying product requirements; researching, designing, modifying, and testing manufacturing processes and solutions during project development.
• Participates in Design for Manufacturing and Assembly study with Design Engineers.
• Participates in Design Review, Design Verification, dFMEA, pFMEA and aFMEA activities.
• Design fixtures based on output of dFMEA activities.
• Perform other tasks as assigned by the supervisor.
JOB REQUIREMENTS
• Degree, MSc or PhD in Mechanical, Electrical or Biomedical Engineering.Technical Diploma with minimum 5 years in Medical Device Development.
EXPERIENCE
• At least 2 years of experience in the medical device industry including concept definition, prototype manufacturing, prototype testing and design documentation.
• Technical Diploma with minimum 5 years in Medical Device Development.
• Experience in simulation software (Abacus, CREO Simulate, etc.).
SKILLS
• Excellent command of Computer Aided Software (CREO, Solidworks or equivalent).
• Strong knowledge of technical standards (ASME, JIS, etc.).
• Competent in data analysis tools like DOE, Minitab.
• Strong command of English (Written and Oral).
• Strategic thinking.
• Resourceful and innovative.
• Independent and has the ability to work under pressure.
• Able to work cross-functionally to develop specific plan to address different challenges.