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Engineer - Should Cost/Value Engineer

2 days ago 2026/10/24
Other Business Support Services
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Job description

Work Flexibility: Onsite




What you will do:



  • Good understanding of manufacturing processes and design of mechanical parts for driving evaluation of cost.



  • Understanding of metals/plastics/additive manufacturing processes and cost derivatives.



  • Good knowledge of manufacturing processes, materials, product, and process design.



  • Understands Should Costing, Zero based, parametric cost modelling and cost benchmarking.



  • Learn and practice use of value engineering tools/Analysis and templates to drive consistency across all efforts and produce outputs throughout the agile cost sprint execution.



  • Liaise with various functional stakeholders to get inputs into building should cost models.



  • Implementing Value Engineering activities for cost reduction/optimization using DFM/A tool.



  • Developing cost models for different unconventional manufacturing setups for quick cost reference using costing tool/software.



  • Closely working with stakeholders in presenting the project insights in the form of Microsoft PPT in a simple & effective manner to support supplier negotiations & guide them in taking critical business decisions.



  • Tear down of different commodity products, identifying material & manufacturing process, BOM creation.



  • Must be able to read and interpret complex engineering drawings and have the ability to understand geometrical dimensioning and tolerancing (GD&T).



  • design, develop, modify, and verify mechanical components for medical devices



  • Assist with prototyping and bench testing



  • Support problem solving, root cause analysis, identify potential solutions, and evaluate them against requirement



  • Understand the product’s intended use and clinical procedures



  • Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements



  • With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures



  • Learn R&D procedures like design controls and risk management, per the Quality Management System



  • With supervision, work with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success



  • Learn procedures, policies, processes, systems, and technology required



  • Work on problems in limited scope; purposefully learn while gaining experience




What you will need:




Minimum Qualifications (Required):



  • Engineering degree (or equivalent knowledge) with 3+ years of experience as minimum/ good professional expertise.



  • Expected to work independently with minimum supervision.



  • Professional knowledge and proven track record of putting it into practice to work cooperatively to ensure project success.



  • Self-starter with demonstrated efficient work methods, analytical & problem-solving skills and ability to handle multiple tasks in a fast-paced environment.



  • The individual should enjoy working in a fast paced, dynamic and results orientated team environment.



  • Excellent Interpersonal Skills - able to express ideas and collaborate effectively with multidisciplinary teams.



  • Innovative thinker - should be able to envisage new and better ways of doing things.



  • Excellent analytical skills, ability to plan, organise and implement concurrent tasks.



  • Experience in an FDA regulated or regulated industry beneficial.



  • High level of PC Skills required.



  • Fundamental knowledge and understanding of mechanical engineering practices and tools, design principles within a regulated environment.



  • Basic knowledge of design and concept generation CAD or CAE modeling tools



  • Basic knowledge of analysis tools and statistical methods



  • Basic knowledge of materials and manufacturing methods



  • Ability to read and Interpret complex drawings






Travel Percentage: 10%








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