R&D Engineer, Process Development (Medical Devices)

  • Location

    Singapore

  • Sector:

    Engineering & Manufacturing

  • Job type:

    Permanent

  • Salary:

    S$5500 - S$6500 per month

  • Contact:

    Abhik Damani

  • Contact email:

    abhik.damani@voltasia.com.sg

  • Job ref:

    BBBH9555_1627031744

  • Published:

    about 2 months ago

  • Expiry date:

    2021-08-22

My client is a global name in the medica device industry and now seek an experienced R&D Process Development Engineer

  • Global Name
  • High Salary
  • State of the art innovation

The candidate will be based in Europe for 12 months and then return to Singapore

Responsibilities:

  • Lead and participate in R&D projects (translation of market requirements into technical requirements, design development, verification) and execute policies, process methods and generate documentation
  • Assume responsibility for the coordination of production introduction including process optimizations, product validation and product approval.
  • Establish and maintain effective communication manufacturing and quality department, R&D and other stakeholders.
  • Develop products and qualify and integrate new technologies and materials through utilization of extensive technical knowledge in compliance with the external standards
  • Ensure quality in a product's design for usability, reliability , marketability and manufacturability
  • Support the product development through aspects of product design criteria, product function and customer needs, complaint assessments, animal studies and supplier contacts
  • Assess the feasibility of new product specifications and definition of specific product requirements in product specification
  • Support product design verification and validation taking design and production processes into consideration
  • Conduct risk assessment of the product and the product components
  • Prepare reports by collecting, analyzing and summarizing information and trends
  • Analyze statistical data and product specifications to determine standards and establish quality and reliability objectives
  • Ensure that standard operating procedures, company policies and procedures are adhered to

Requirements:

  • Degree in Mechanical, Electrical, Chemical Engineering or equivalent
  • 3-5 years of work experience in R&D, product/process development from a medical/biotech industry
  • Experience with manufacturing processes, automation and methods
  • Experience working within a quality and design controlled environment and familiar with ISO13485 and GMP
  • Knowledge in the verification and validation of medical devices
  • Team player with strong organizational, interpersonal, communication and intercultural skills

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).