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Mechanical Engineer

People Prime Worldwide

2 - 5 years

Bengaluru

Posted: 10/01/2026

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Job Description

About Company :

They balance innovation with an open, friendly culture and the backing of a long-established parent company, known for its ethical reputation. We guide customers from whats now to whats next by unlocking the value of their data and applications to solve their digital challenges, achieving outcomes that benefit both business and society.


About Client:

Our client is a global digital solutions and technology consulting company headquartered in Mumbai, India. The company generates annual revenue of over $4.29 billion (35,517 crore), reflecting a 4.4% year-over-year growth in USD terms. It has a workforce of around 86,000 professionals operating in more than 40 countries and serves a global client base of over 700 organizations.

Our client operates across several major industry sectors, including Banking, Financial Services & Insurance (BFSI), Technology, Media & Telecommunications (TMT), Healthcare & Life Sciences, and Manufacturing & Consumer. In the past year, the company achieved a net profit of $553.4 million (4,584.6 crore), marking a 1.4% increase from the previous year. It also recorded a strong order inflow of $5.6 billion, up 15.7% year-over-year, highlighting growing demand across its service lines.

Key focus areas include Digital Transformation, Enterprise AI, Data & Analytics, and Product Engineeringreflecting its strategic commitment to driving innovation and value for clients across industries.


Job Title: Med Devices Sustenance Engineer

Location: Bengaluru

Experience: 6+ Years

Job Type : Contract to hire.

Notice Period: Immediate

Job Summary:

  • Bachelors Degree in Mechanical Engineering or a related field.
  • 6+ years of experience in medical domain ( electro mechanical products-- class II and class III).
  • Hands on exp in SolidWorks and Siemens NX, Design for manufacturability, and serviceability for plastics and sheet metal ,exp in Stack-up analysis.
  • Regulatory compliance alignment knowledge including ISO 13485, IEC 60601, ISO 14971, Understanding of FDA design control requirements (21 CFR 820.30).
  • Working experience in EUMDR requirements ( Gap assessment and remediation).
  • Experience in FMEA, Verification and Validation testing. Develop Test plans, Engineering analysis for complex design/process issues and providing rationale, Verification and Validation plans and protocols.
  • Experience in ECO/ECN and its related Process and PDM and PLM Tools.
  • Experience of Non-Conformance Evaluation.
  • Experience of working on Design History Files and Technical Files
  • Work experience on obsolescence management.
  • Client interaction, Weekly status reports, Multiple stake holder interaction

Qualifications:

  • Bachelors degree in engineering and related field.

Seniority Level

  • Mid-Senior level

Industry

  • IT Services and IT Consulting

Employment Type

  • Contract

Job Functions

  • Business Development
  • Consulting

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