Engineer - Should Cost/Value Engineer

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%