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Engineering 🏢 Full Time ⭐️ Terverifikasi

R&D Engineer I - Medical Device Innovation

Boston Scientific
Denpasar, Bali, Indonesia
Salary Estimate
Rp 250.000.000 – Rp 400.000.000
Newest
Live Update
7 Agustus 2026
Deadline
7 Agu 2027

job description

Join Boston Scientific, a global leader in medical technology, as an R&D Engineer I in our dynamic team based in Bali, Indonesia. This role is part of our Interventional Cardiology and Vascular Therapies (ICVT) Sustaining division, where you will contribute to cutting-edge innovations that improve patient lives worldwide.

As an R&D Engineer, you will collaborate with cross-functional teams to design, develop, and enhance medical devices that set industry standards. Your work will directly impact the sustainability and performance of our life-saving products, ensuring they meet the highest quality and regulatory standards.

We offer a competitive salary, a culture of innovation, and the opportunity to work on transformative projects in a tropical paradise. If you are passionate about engineering excellence and making a difference in healthcare, we invite you to apply.

Responsibility

  • Design and develop medical device components and systems in compliance with industry regulations (e.g., FDA, ISO 13485).
  • Collaborate with cross-functional teams (e.g., manufacturing, quality assurance) to ensure product sustainability and performance.
  • Conduct feasibility studies, risk assessments, and design verification/validation testing.
  • Troubleshoot and resolve technical issues in existing products to enhance reliability and efficiency.
  • Document technical specifications, test protocols, and reports for regulatory submissions.
  • Support the transfer of new products from R&D to manufacturing.
  • Stay updated on emerging technologies and industry trends to drive innovation.
  • Participate in design reviews and provide technical expertise to stakeholders.

Qualifications

  • Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, or a related field.
  • 1-3 years of experience in medical device R&D, product development, or sustaining engineering.
  • Strong knowledge of design control processes, GD&T, and medical device regulations (e.g., ISO 13485, 21 CFR Part 820).
  • Proficiency in CAD software (SolidWorks, AutoCAD) and FEA analysis tools.
  • Experience with material selection, prototyping, and testing for medical applications.
  • Excellent problem-solving, analytical, and communication skills.
  • Ability to work in a fast-paced, collaborative environment.
  • Familiarity with Six Sigma, Lean Manufacturing, or DFMEA is a plus.

Required Skills

Medical Device R&D Product Development CAD (SolidWorks AutoCAD) GD&T ISO 13485 FDA Regulations Design Control Prototyping Testing Six Sigma DFMEA Cross-functional Collaboration

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