Engineering Manager, Medical Devices

Volt Asia

Job Description

My client is a world leader in the design, development and manufacturing of complex medical devices and now seek an experienced Engineering Manager to join them

  • Global Name
  • Innovative Products
  • State of the art technology

Responsibilities:

  • Assume responsibility to lead and manage the entire product development life cycle
  • Establish and manage the entire end-to-end supply chain and production process by working with contract manufacturers
  • Set up good manufacturing practices and quality control systems and manage post-sales engineering services
  • Plan and monitor product development projects across multiple cross functional teams to ensure appropriate execution and delivery
  • Lead design control activities and apply technical expertise to the design and development of new products
  • Spearhead risk management activities and provide technical expertise regarding identification and mitigation of design and use risks
  • Ensure project statuses are properly documented and presented
  • Collaborate with internal document control and integrate and maintain project related documents and information
  • Review and analyze project activities and costs to determine progress toward business objectives
  • Determine patentable ideas and work alongside IP department
  • Recruit likeminded technical experts (engineering, manufacturing, R&D, quality)
  • Ensure an atmosphere of learning, six sigma, and continuous process improvement is implemented

Requirements:

  • Advanced Degree in Mechanical, Electrical, Chemical engineering or equivalent with at least 10 years' R&D and manufacturing experience from the medical device/consumer electronics industry
  • Stronghold in manufacturing processes for complex medical devices
  • Extensive experience in product development process from concept development to prototyping and design/documentation release to manufacturing.
  • Prior background in managing contract manufacturers and EMS providers
  • Working experience in a cGMP, ISO 13485 facility will be a big plus
  • Ability to lead a team and manage multiple internal and external stakeholders

Please send your resume in WORD format by clicking the apply button below or contact Abhik Damani on +65 6701 1527 for a confidential discussion. Please note that only short-listed candidates will be contacted. CEI Reg. Number R1544061 (Abhik Damani).

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