Process Development Engineer

Develop new or improve existing processes of manufacturing.

Supporting other departments in problem-solving if there are problems/ technical issues with mechanical/ electronic tools.

Design CAD/CAM, prototyping/ fabrication, qualification, implementation, and documentation control.

Supporting others in problem-solving if there are problems with mechanical tools.

Support in-house machining process.

Collaborating with Quality teams to investigate, analyze, develop and implement for all quality aspects.

Responsible for handling documentation (WI / MI / IQOQPQ) of new/existing projects or updated existing manufacturing processes.

Able to manage and implement the Project Management timeline.

Requirements

Education, min. Diploma Degree (D3) in Mechanical/ Manufacturing/ Mechatronics/ Industrial/ Electronic engineering.

Minimum 2 years experience in a tool maker or manufacturing environment.

Experience with process improvement and developing manufacturing processes.

Knowledge and experience with Lean Manufacturing Implementation.

Experience with PLC and Micro Controller.

Experience with Special Purpose Machine.

Knowledge and experience with IoT.

Knowledge and experience with Solidwork CAD, Fusion CAM, 3D printer, Stamping process, Molding process, CNC Milling, and CNC Lathe.

Strong analytical and problem solving skills.

Knowledge and understanding of ISO 9001 and related quality standards.

Proactive and looking for improvement opportunities on own initiative.

Able to communicate in English (writing and verbal).

Microsoft Office.

Technomed Asia is a foreign owned company specialized in the production of medical accessories. Main products are electrodes for EEG (brain studies), EMG (muscle studies) and intra‑operative monitoring. Technomed Asia produces accessories under the Technomed brand, as well as for several OEM customers worldwide. Its strength is the production of relatively small quantities of highly customized products. Technomed Asia has its own independent ISO 13485 certified quality system and is FDA registered as well as appointed as a manufacturer of medical accessories for the Japanese market.

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