Sr. Mechanical Engineer

Philips


Date: 1 day ago
City: Pune, Maharashtra
Contract type: Full time
Job Title
Sr. Mechanical Engineer

Job Description

Job title: Sr. Mechanical Engineer

In this role, you will have the opportunity to participate in an exciting and progressive environment, developing products that save lives. You will be part of the NPI (New Product Introduction) Mechanical Engineering Team within the R&D (Research and Development) Department at Philips SRC (Sleep and Respiratory Care) division. You will be directly involved in the design and development of Ventilators and disposables (masks).

Your Role:
  • Support Windchill PLM implementation, data migration and software validation tasks initially (for a period of over an year).
  • Support DHF (design history file) remediation for mechanical engineering deliverables which includes - defining strategy and planning, gap analysis, creating new and revising DHFs, reviewing and releasing DHFs.
  • DHFs accountability and responsibility for mechanical and mechatronics parts and sub-systems (Gas path, valves, sensors (air, O2 and Pressure), manifold, patient interface, solenoid valves, filters, blowers, motors and enclosure).
  • Review, mentor correctness and approve design documentation including requirements specifications, design docs, engineering analysis & simulation studies, calculations, capture, test plans, test procedures, test records & reports.
  • Lead project team members to produce development plans and identify and mitigate development risks.
  • Conceive, design, develop, evaluate and implement new systems and products in the field of medical ventilator product development and sustaining engineering.
  • Utilize best practices in mechanical design analysis, modeling and tolerance analysis to produce a highly viable mechanical.
  • Create documentation, including component details, assembly details, incoming and finished inspection requirements using CAD (Computer Aided Design) as a design tool.
  • Responsible for all aspects of design documentation including requirements specification, engineering analysis, drawings, test plans/procedures, validation, the release of components, assemblies and products to production and production start-up support.
  • Supports the manufacturing engineering team in troubleshooting and resolving issues discovered during production.
  • Be a self-starter, action-oriented, organized and disciplined.
  • Keep abreast of technical developments in own field through literature, technical contacts and industry competition.
  • Work in close co-ordination with PMG and manufacturing engineering for resolution of issues as they arise during sample build phases and actual production.
  • Lead & support CAPA activities for closure of CAPA with effective implementation of containment, corrective and preventive actions.
  • Lead RCA investigation for any issues arises in the plant or in the field using fish bone diagrams, probable and potential causes, why-why analysis, replicating issues in the lab and taking containment and corrective actions for re-occurrence prevention.

You're the right fit if:
  • Bachelor’s or master's degree in Mechanical Engineering.
  • Minimum of 4 years' experience in the design and analysis of medical devices.
  • Experience in design and analysis of medical ventilators or medical gas delivery systems a plus.
  • Experience leading a technical team in product development
  • In depth knowledge of pneumatic systems including pressure and flow sensing.
  • Experience in the design and analysis of low and medium pressure gas valves.
  • Experience with low pressure gas blowers.
  • Experience with Computational Fluid Dynamics.
  • Experience in the design of plastic injection molded parts.
  • Knowledge of ASME (American Society of Mechanical Engineers) Y14.5 Dimensioning and Tolerancing.
  • Proficiency with solid modeling CAD software (Pro-E/Creo a plus).
  • Good mechanical aptitude and solid understanding of mechanical engineering principles.
  • Effective communication skills, both oral and written.
  • Familiarity with FDA (Food and Drug Administration (USA)) quality systems including ISO13485, 21CFR Part820 (a plus).

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.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

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