R&D Senior / Mechanical Engineer (custom mechanism) - Tuas West Road

at  SEARCH STAFFING SERVICES PTE LTD

Our client is a emergent brand name in the medical technology (Medical Electronics – Medical Devices) sector. We are looking for like-minded individuals who are passionate to join them to develop their next generation of medical electronics.

REQUIREMENTS

• Bachelor degree or above in Mechanical Engineering
• Minimum 2 - 7+ years’ in Mechanical Engineering experience in at least 2 complete product lifecycles i.e. from product conceptualization to design, development.
• Electro-mechanical integration and exposure
• Solid understanding of general manufacturing process like injection molding, sheet metal fabrication, machining with knowledge in tool engineering and design
• Familiar with prototyping techniques and tooling DFM, 3D modelling with Creo/Solidworks
• Familiar with preparing 2D drawings with GD&T.
• Able to perform tolerance analysis.
• Familiar with fluid dynamics, CFD analysis
  Interested applicants, kindly send in a copy of your updated resume in WORD document to hr@searchstaffing.com.sg stating your current and expected remuneration together with notice period required to current employer.
  You can also contact Vincent Low for a confidential discussion at 6749 4236.
  EA Personnel Registration No: R132470

• You will be part of a team of R&D engineers in Singapore including engineers from the Mechanical, Software, Electronics and Systems Engineering discipline.
• Perform mechanical engineering activities to develop new Products from concept to production
• Perform engineering activities required for support of released products for product development, quality improvement, COGS reduction, and manufacturing issues resolution
• Work with other simulation/electronic/mechanical engineers to ensure product performance, reliability and cost expectations are met.
• Lead projects related to cost, quality, design, and productivity using methodology such as Tolerance Stack, Process Capability (Cpk), FMEA, Minitab, etc.
• Operate within a project team and assume responsibility to design, develop and verify new products from concept through to production
• Participate in the preparation and review of system documentation including System Specifications, Regression Analyses, Risk Analyses, Regulatory Submissions
• Testing, verification, and validation of products and alterations to ensure they meet the necessary requirements and specifications
• Identify gaps in design proposals, technical capabilities/techniques, and supports the development of strategies to overcome them through DFM & DFS practices.
• Conduct technical design reviews at system or subsystem levels in projects.
• Work within medical regulatory requirements (FDA, ISO, IEC)