About this role
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%