job description
Join Masimo, a global leader in innovative medical technology, as a Process Engineer in beautiful Bali. In this role, you will play a pivotal part in maintaining and optimizing manufacturing processes to minimize downtime and ensure the highest product quality standards. Your expertise will directly impact the efficiency and reliability of our production lines, contributing to our mission of improving patient outcomes worldwide.
Based in one of Bali's vibrant locationsâCanggu, Ubud, Denpasar, Jimbaran, Nusa Dua, Kuta, or Badungâyou will collaborate with cross-functional teams to drive continuous improvement initiatives, troubleshoot process inefficiencies, and implement cutting-edge solutions. This is a unique opportunity to combine your technical skills with the inspiring work environment of Bali, fostering both professional growth and work-life balance.
If you are passionate about engineering excellence and eager to make a tangible difference in the medical technology field, we invite you to apply and become part of our dynamic team.
Responsibility
- Develop, maintain, and optimize manufacturing processes to enhance efficiency, reduce waste, and improve product quality.
- Conduct root cause analysis for process deviations and implement corrective and preventive actions (CAPA).
- Collaborate with production, quality assurance, and R&D teams to ensure seamless process integration and compliance with regulatory standards.
- Design and execute process validation protocols, including IQ, OQ, and PQ, to ensure consistent product performance.
- Monitor key performance indicators (KPIs) and utilize data-driven insights to drive continuous improvement initiatives.
- Train and mentor production staff on best practices, process controls, and safety protocols.
- Evaluate and recommend new technologies, equipment, or methodologies to enhance manufacturing capabilities.
- Prepare and maintain comprehensive documentation, including process flow diagrams, work instructions, and standard operating procedures (SOPs).
Qualifications
- Bachelor's degree in Mechanical Engineering, Industrial Engineering, Chemical Engineering, or a related field.
- Minimum of 3 years of experience in process engineering, preferably in the medical device, pharmaceutical, or manufacturing industry.
- Strong knowledge of lean manufacturing, Six Sigma, or other continuous improvement methodologies.
- Proficiency in process validation, statistical process control (SPC), and root cause analysis tools (e.g., 5 Whys, Fishbone Diagram).
- Experience with CAD software, process simulation tools, or manufacturing execution systems (MES) is a plus.
- Excellent analytical, problem-solving, and project management skills.
- Strong communication and interpersonal skills to effectively collaborate with cross-functional teams.
- Familiarity with regulatory standards such as ISO 13485, FDA QSR, or GMP is highly desirable.