Philips Mechanical Designer - STET 

India, Maharashtra 

287707719

Mechanical Designer - STETJob Description

You will be responsible for driving meaningful and innovative product development, generating ideas/concepts in feature development to improve quality and reduce cost, as well as performing the role of a technical lead in taking the product development through manufacturing release while transferring products between suppliers and manage sustaining of different devices by following PDLM-MLD process.

To be part of an exciting team and contribute to the design, development and maintenance of Diagnostic Imaging (MRI, CT/AMI, DXR etc.) components and products. In this role of, you are responsible for the development and maintenance of Image Acquisition Platform (IAP) - Hardware Systems/Subsystems and will gain substantial knowledge of complex systems in medical imaging environment. Together with a multidisciplinary team of engineers, you play a crucial role in getting these systems/sub-systems to the required performance, by understanding the electrical, electronics and controls and looking for the best solutions within those boundaries. This requires broad orientation, conceptual skills and a “can do” mentality, keeping abreast with all trends and
You are responsible for

• Leading the development and release of system/ electro-mechanical modules or reverse engineer existing products to improve overall long term system quality, reliability, yield rates, and cost effectiveness.

• Working with a cross-functional team to ensure the design and development of electro-mechanical components to meet the needs of the internal and external customers.

• Working with design partners/suppliers and lead product development activities from design concept to manufacturing release.

• Using modelling and simulation tools to create and modify architectures, 3D designs, and 2D drawings.

• Drive continuous improvement projects related to design implementation, manufacturing process, product quality and reliability.

• Requirements, design, implementation, test and integration of module/sub-system in accordance with the higher-level architectural requirements and design specifications

• Ensuring that the design is consistent with the higher-level architecture and requirements

• Ensuring that the proposed design would have the safety, reliability and quality features built-in

• Responsible for ensuring that the design meets the performance, quality and cost criteria

• Conduct concept and feasibility studies. Leads the introduction of new technologies

• Ensuring that there is proper documentation per standards for the developed design

• Ensuring the mutual consistency and efficient integration of the separate components in modular design that meets the product specification

• Ensuring that his design modules meet the product certification requirements

• Drawing up personal schedule and reports on progress

• Defining and assessing the Work Breakdown Structure/planning/costs of his/her area

• Being abreast of technical developments in own field through study of literature and technical contacts

• Maintaining product and company reputation by complying with country specific regulations

• Supplier evaluation and communication

To succeed in this role, you shou

• M.Tech / B.E/ B.Tech in Mechanical/ Electrical/ Electronics or Equivalent Engineering

• 10+ years of relevant experience in design & development of electro-mechanical sub-systems & systems.

• Strong communication and collaborative abilities proactively seeks out expertise and advice and input from others in a collaborative team-environment.

• Experience in developing the requirements for electro-mechanical assemblies.

• Knowledge in part qualification and statistical process studies such as CP and CPK and be able to work with suppliers to improve part process capability.

• Experience in lifecycle testing and verification activities of cables to meet functional and lifecycle requirements.

• Experience working with suppliers and design partners, including part/module development and resolving technical issues.

• Strong technical writing/ documentation skills for regulated medical device design environment, including requirements definition.

• Knowledge of good design practices and experienced with DFMEA.

• Knowledge of EMI/EMC standards and testing for conformance

• Knowledge of mechanical design compatibility aspects

• Knowledge of IEC 60601 standards will be an added advantage

• Knowledge of Embedded Software Programming will be an added advantage

• Ability to understand and debug problems across hardware/software boundaries

• Knowledge of Global Medical Quality and Regulatory Standards e.g. IEC, FDA, UL, CE, CSA etc.

• Demonstrated ability to effectively work with cross-functional stakeholders to ensure the design meets their expectations and needs, and that the needs/requirements are properly documented.

• Experience with document control systems (E-Matrix, Agile) and FDA/ISO regulated medical device design environment.

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