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Engineering 🏢 Full Time ⭐️ Terverifikasi

Supplier Project Engineer - Medical Devices (Bali, Indonesia)

Insulet
Bali, Indonesia
Salary Estimate
Rp 18.000.000 – Rp 25.000.000
Newest
Live Update
17 Juli 2026
Deadline
17 Jul 2027

job description

Join Insulet, a global leader in innovative medical device technology, as our Supplier Project Engineer in beautiful Bali, Indonesia. In this critical role, you'll bridge the gap between our world-class manufacturing operations and our strategic suppliers, ensuring seamless project execution and superior product quality for our life-changing diabetes management solutions.

As part of our growing team in Bali, you'll collaborate with cross-functional leaders in Quality, Sourcing, and Manufacturing to drive supplier performance, optimize processes, and deliver projects on time and within budget. This is an exceptional opportunity to work with cutting-edge medical technology while enjoying Bali's unique work-life balance in locations like Canggu, Ubud, or Kuta.

Insulet's mission is to improve the lives of people with diabetes through our revolutionary Omnipod® system. As a Supplier Project Engineer, you'll play a vital role in ensuring our supply chain meets the highest standards of quality and reliability. This position offers professional growth, competitive compensation, and the chance to make a real difference in healthcare technology.

We're looking for a detail-oriented professional with strong technical and communication skills to join our dynamic team. If you're passionate about medical technology and want to work in one of the world's most desirable locations, we'd love to hear from you.

Responsibility

  • Lead supplier development projects from concept to implementation, ensuring alignment with Insulet's quality standards and business objectives
  • Collaborate with cross-functional teams (Quality, Sourcing, Manufacturing) to optimize supplier performance and resolve technical issues
  • Develop and maintain project timelines, budgets, and risk assessments for supplier-related initiatives
  • Conduct regular supplier audits and performance reviews to ensure compliance with medical device regulations (ISO 13485, FDA)
  • Drive continuous improvement initiatives to enhance supplier quality, delivery, and cost efficiency
  • Facilitate communication between internal teams and suppliers to ensure clear requirements and expectations
  • Prepare and present technical reports and project updates to senior management
  • Support new product introductions by coordinating with suppliers on design transfers and validation activities

Qualifications

  • Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or equivalent experience
  • 3+ years of experience in supplier management, project engineering, or manufacturing engineering, preferably in medical devices or regulated industries
  • Strong understanding of quality management systems (ISO 13485, FDA 21 CFR Part 820) and supplier audit processes
  • Proven project management skills with experience using tools like MS Project or JIRA
  • Excellent communication skills in English (written and verbal) with ability to work in multicultural teams
  • Experience with Lean Manufacturing, Six Sigma, or continuous improvement methodologies is a plus
  • Ability to travel domestically and internationally as needed (up to 20%)
  • Problem-solving mindset with strong analytical and technical skills

Required Skills

supplier management project engineering quality management systems medical device regulations cross-functional collaboration technical documentation continuous improvement Lean Six Sigma risk assessment MS Project JIRA ISO 13485 FDA compliance

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