Senior Design Engineer

Marmon Technologies India Private Limited

As a part of the global industrial organization Marmon Holdings—which is backed by Berkshire Hathaway—you’ll be doing things that matter, leading at every level, and winning a better way. We’re committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone’s empowered to be their best.

This Senior Designer (Microaire Senior) is responsible for executing and leading product design improvements, cost reduction initiatives, and resolving technical challenges in existing products. This role supports both Sustaining Engineering and Innovation teams, contributing to new product development through design, testing, and validation activities. The engineer will develop detailed models, specifications, and documentation while collaborating closely with cross-functional leaders to deliver robust, high-quality engineering solutions.

Mandatory Skills:

• 3+ years of experience in creating and executing Change Orders, including design updates, 3D models, drawings, and supporting documentation such as change justifications, tolerance analyses, and verification testing.
• Proficiency in 2D drafting and 3D modelling, preferably using SolidWorks and Strong knowledge of ANSI Y14.5 geometric dimensioning and tolerancing standards.
• Experience in Implement design control updates for product improvements or post-market activities (e.g., field failures, customer complaints, or research findings).
• Strong communication and interpersonal skills with the ability to manage multiple priorities and deliver within project timelines.

Desired Skills:

• Prepare and submit Change Requests and support approval workflows.
• Create and execute Change Orders, including design updates, 3D models, drawings, and supporting documentation such as change justifications, tolerance analyses, and verification testing.
• Implement design control updates for product improvements or post-market activities (e.g., field failures, customer complaints, or research findings).
• Contribute to updates of Product Trace Matrices, Risk Analyses, and Usability Engineering documentation.
• Support regulatory documentation by providing inputs for Technical File updates, FDA submissions, or registration support for global markets.
• Collaborate with Product Innovation and Product Strategy teams to assist in user evaluations, usability testing, and design validation for both sustaining changes and new product development.
• Support Design Verification activities, including developing test methods, performing analyses, and reviewing results to confirm compliance with design inputs.
• Work closely with Manufacturing Engineering to ensure effective design transfer, including review of manufacturing instructions and inspection criteria.
• Coordinate with external resources such as suppliers, prototype vendors, and material providers to support design execution.
• Collaborate cross-functionally with Project Management, Quality, Regulatory, and Testing teams to deliver design tasks on schedule and per standards.
• Proficiency in 2D drafting and 3D modelling, preferably using SolidWorks.
• Strong knowledge of ANSI Y14.5 geometric dimensioning and tolerancing standards.
• Solid understanding of mechanical component and assembly design, including material selection, part tolerancing, tolerance stack-up analysis, and mechanical stress analysis.
• Familiarity with metallic and polymer materials commonly used in precision or medical applications (stainless steel, aluminium, engineered plastics).
• Working knowledge of manufacturing processes such as machining, injection moulding, additive manufacturing, and finishing techniques.
• Awareness of factors influencing durability and reusability of mechanical or surgical instruments (corrosion, wear, sterilization, and thermal cycling).
• Basic understanding of design verification and validation methodologies, test development, and data analysis
• Exposure to design control processes under ISO 13485, ISO 14971 (Risk Management), and CFR Title 21 Part 820.30.
• Awareness of IEC 62366 (Usability Engineering) principles.
• Proficient in Microsoft Office, Project, and other engineering documentation or analysis tools.
• Ability to manage multiple technical tasks and deliverables in a regulated environment.

Opportunities for Growth

• Gain comprehensive exposure to global product and process development through hands-on involvement in engineering and validation tasks.
• Enhance technical competence in SolidWorks, medical devices, and U.S.A Norms.
• Collaborate with international engineering teams, strengthening global exposure, communication, and teamwork skills.
• Progress into roles such as Lead Design Engineer based on performance and capability growth.

Required Qualifications

• Graduation in Mechanical Engineering, (or equivalent work experience) with 3 -6 Years (Medical device product development experience is preferred)
• A seasoned, result-oriented engineer who can work independently once given direction, has good rapport with coworkers, can listen, be creative, and is detailed oriented.
• Strong analytical and problem-solving abilities, driven by a curious and self-motivated approach, with the capability to work independently and with minimal supervision.
• Excellent communication and collaboration skills, with experience working in global engineering teams and effectively engaging across cross-functional environments.
• Maintains a good attitude, persistence, and drive focused on finding a way to accomplish the objectives. 
• Flexible in adapting to quickly changing business & task/ project priorities, ability & willingness to travel locally, nationally, or internationally when required.

Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.