Mechanical Designer

Philips International; Pimpri; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Philips is seeking a Mechanical Designer to join the Mechatronic Development Cluster within the IGT Fixed Systems R&D team. You will contribute to the development of mechanical designs for medical devices, including enclosures, sheet metal, plastics, and assemblies, using V-model processes.

Responsibilities include thermal simulations, FEA, design reviews, and ensuring documentation such as FMEA and DFMA are maintained.

Qualifications

• Bachelor’s or Master’s degree in mechanical engineering.
• Minimum of 5+ years of relevant R&D experience in medical domain.
• Experience in product design, development, and maintenance of released products.
• Hands on experience in NPI End to End workflows.
• Excellent design documentation skills and proficient English communication.

Responsibilities

• Contribute to requirements, design, implementation, test and integration per specifications.
• Coordinate with operations, procurement, and other stakeholders.
• Develop/review thermal simulation models and FEA, stack-up tolerances.
• Ensure proper documentation (DFMEA, FMEA, DFMA, design calculations).
• Participate in design reviews and risk assessments (FMEA) and supplier communication.
• Support sourcing strategy including supplier selection and contract management.

Skills

Mechanical design

NPI end-to-end

English communication

Education

Bachelor’s or Master’s in Mechanical Engineering

Tools

FEA

Thermal simulation

Job description

Mechanical Designer

Mechanical Designer As a Mechanical Engineer, you will play a key role in the development of various mechanical designs like user interfaces, switches, display enclosures including plastic & metal, ceiling suspension, thermal simulation, Packaging and labelling etc. in the new product designs for Philips Image Guided therapy. In this role, you will contribute to developing components and system elements using the V-model methodology while aligning with user needs, product requirements, and business objectives. You will apply internal and external research insights, leverage emerging technologies, and ensure robust system-level thinking throughout the design lifecycle. Your work will contribute directly to delivering high-quality, reliable, and innovative solutions that enhance performance and enable exceptional clinical experiences.

Your Role

Within new product introduction projects and product life cycle activities you contribute to requirements, integral design, implementation, test and integration in accordance with the higher-level specifications. Including alignment with all the relevant internal and external stakeholders such as operations and procurement. Develop/ Review thermal simulation models, FEA, stack up tolerance etc. Good understanding of manufacturing processes related to sheet metal, casting, plastics and machining parts. Ensure that there is proper documentation for the design (e.g. Design calculations, FMEA, DFM, DFMA, FMEA, VAVE, Field data analysis, verification reporting); Ensure the mutual consistency and efficient integration of the separate modules in modular, easy-to-maintain units that meets the product specification. Contribute to the sourcing strategy including make-buy decisions, supplier selection, and contract management. Creating and/or participating in design reviews and risk assessments (e.g. FMEA) Alignment with other functions (Electrical, mechatronics, norm compliance, test and validation, purchase, quality, other). Conducting early integration tests on predefined prototypes and addressing supplier issues will also be your responsibility. You will follow up on any necessary actions. Your role will require performing all tasks in line with established department processes. You are a part of Infrastructure department in Mechatronic Development Cluster within the IGT Fixed Systems R&D organization. The department consists of an open and multi-cultural team working towards new product introductions (NPI) of image guided therapy system.

You are fit if

• Bachelor’s or master’s degree in mechanical engineering or equivalent
• Minimum of 5+ years of relevant R&D working experience in medical domain
• Experience in product design, development, and maintenance of released products
• Hands on experience in NPI End to End way of working
• Analytical and Methodological mindset and good hold on processes
• Excellent design documentation skills
• Result oriented and self-steering with a problem-solving attitude
• Ability to work independently & to act proactively
• Good command of English (both written and verbal)
• Work experience in Agile Release Trains following SAFe framework will be a plus
• Quality mindset, A Six Sigma Green Belt will be a plus
• Experience with Regulatory aspects, Knowledge of FDA guidelines and compliance requirements for medical (ISO13485, FDA) will be preferred
• Translating customer needs into technical requirements and then creating mechatronic solutions

How we work together

We believe that we are better together than apart. For our office-based teams, this means working in- person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This role is an office-based role.

About Philips

We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others. Learn more about our business. Discover our rich and exciting history. Learn more about our purpose.

We believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life. For more than 130 years, we have been creating technologies and innovations that improve people’s lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health. Together, we deliver better care for more people because we believe that every human matters. That's why we're taking steps to create an environment where we acknowledge and embrace our differences and uniqueness and listen to and value each other's views. When people feel cared for and listened to, they bring their best qualities to work, leading to better collaboration, communication, innovation and success.

It is the policy of Philips to provide equal employment and advancement opportunities to all qualified employees and applicants for employment without regard to race, color, religion, sex, pregnancy/childbirth or related medical conditions, age, ethnic or national origin, sexual orientation, gender identity or expression, physical or mental disability, genetic information, citizenship status, veteran or military status, marital or domestic partner status or any other characteristic protected by law. As an equal opportunity employer, Philips is committed to fostering a culture where all are treated with respect and professionalism. To ensure reasonable accommodations for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veterans' Readjustment Act of 1974 and Title I of the Americans with Disabilities Act of 1990, applicants that require accommodation in the job application process may contact 888-367-7223, option 5, for assistance. Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug-free workplace. Know Your Rights.