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New Product Development - Manager

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Onsite

New Product Development - Manager

Mais India Medical Devices Pvt Ltd

New Product Development - Manager

Skills

Testing & QAProcess Improvement

1 year ago

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Important information


Contract type:

Permanent

Location:

Gurugram, Haryana, India

Work mode:

Onsite

Published on:

14 October 2026

What they need


Job highlights

  • Required minimum 5 year experience in medical device industries.

  • Compile and prepare required documentation

  • Experience

  • Experienced in interfacing with functional groups outside of engineering . Good communication skills,verbal and written .

  • New product design & development initial stage to production stage.

  • Benchmarking of the product.

  • Test and record performance of components, products & manufacturing methods.

  • Analyze and resolve technical issues associated with components, products, manufacturing methods and performance.

  • Prepare bill of materials (BOM), design specifications & raw materials specifications etc.

  • Conduct failure mode & risk analysis according to ISO 13485.

  • Responsible for product design verification & validation and maintain its records.

  • Ensuring Manufacturing performance and Quality goals are met.

  • Prepare and review documentation history files (DHFs). .

  • Maintain and improve existing product manufacturing processes. Anticipate Manufacturing s need for new products and fixtures.

  • To be involved in the assembly, troubleshooting, testing, and repair activities of our products.

  • Provide instruction and support to Manufacturing and QA on manufacturing techniques, procedures, and QC inspections.

  • Survey and identify replacement components for reasons of obsolescence or cost reduction.

  • Identify and contact vendors. Compare technical specifications. Compile and prepare required documentation.

  • Assure the timely manufacturing, packaging, and delivery of new products.

  • Identify, source, and implement improvements in manufacturing procedures.

  • Coordinate relationships with vendors and contractors.

  • Responsible for on-going process improvement: take initiative to define, plan, and execute improvement projects, achieve objectives in increasing yields, reducing cycle time, reducing overall cost, and improving product quality and reliability.

Education

  • Butcher of Engineering or Equivalent

Experience

  • Required minimum 5 year experience in medical device industries.

Knowledge and Training

  • Strong knowledge of medical devices product design and development process.
  • Knowledge of injection multi cavity injection mould, die, fixture and machine design.
  • Knowledge of design and drawing change control procedure.
  • Ability to assess the feasibility of design modifications to existing designs.
  • Experienced in troubleshooting and recommending corrective or preventive actions to improve product reliability.
  • Experienced in interfacing with functional groups outside of engineering
  • Good communication skills, verbal and written
  • Knowledge of ISO 13485 / MDR 2017
  • Strong interpersonal and collaborative skills. Works well as a supportive team member.
  • Knowledge of CAD software Solid Works is desirable.

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