Lead Medical Device Engineer
2 months ago
Nitto Denko Asia Technical (NAT) Centre was established in 2008 and backed by a 100-year-old Japanese corporation, Nitto Denko Corp. NAT is situated in Biopolis, heart of Singapore’s biomedical hub. NAT’s mission is to develop the Integrated Organic Optoelectronic for Biosensor Application. To achieve this mission, NAT is carrying out many concurrent research projects with top research institutions both locally and overseas.
Are you passionate about advancing healthcare technology and saving lives through innovative medical devices? We are seeking an experienced and driven Lead Medical Device Engineer to oversee the development of cutting-edge ECG (electrocardiogram) systems as part of our rapidly growing healthcare division.
In this role, you will lead the design, development, and regulatory approval of state-of-the-art ECG devices that meet the highest standards of medical safety and performance. You will work closely with cross-functional teams, including clinical experts, product managers, and regulatory affairs specialists, to bring groundbreaking products to market. Your leadership and technical expertise will be key to driving innovation and ensuring our devices improve patient care globally.
You will:
- Lead the end-to-end development of ECG medical devices, from initial concept and design to testing, validation, and market launch.
- Collaborate with clinicians, engineers, and product managers to define product specifications and ensure alignment with clinical needs and regulatory requirements.
- Oversee the integration of hardware and software components to ensure the ECG devices meet performance, safety, and usability standards.
- Drive the design of user-friendly interfaces and workflows that enhance the clinical application of ECG devices.
- Ensure compliance with medical device regulations (such as FDA, CE, ISO 13485) and prepare all necessary documentation for regulatory submissions.
- Manage risk analysis, quality control processes, and testing protocols to ensure device safety and reliability.
- Lead the collaboration with external partners, including suppliers, testing laboratories, and certification bodies, to ensure the device meets global standards.
- Stay current with advancements in medical technology and ECG innovations, incorporating the latest scientific research into the product development process.
- Mentor and manage a multidisciplinary team of engineers, providing guidance and fostering an environment of continuous improvement and innovation.
Skills/Qualifications:
- Experience: A minimum of 5 years of experience in medical device development, with a focus on ECG devices or other diagnostic equipment. Proven track record of taking medical devices from concept to market is highly valued.
- Technical Expertise: Strong background in biomedical engineering, electrical engineering, or a related field. Experience with ECG signal processing, device hardware design, and software integration is essential.
- Regulatory Knowledge: In-depth understanding of global medical device regulations (e.g., FDA 510(k), CE marking, ISO standards) and experience with regulatory submissions and compliance processes.
- Project Leadership: Demonstrated ability to lead complex projects, manage cross-functional teams, and coordinate with external stakeholders to deliver high-quality medical devices on time and within budget.
- Problem-Solving: Strong analytical and problem-solving skills, with a proactive approach to identifying issues and developing solutions in the development process.
- Attention to Detail: Rigorous attention to detail in the design, testing, and documentation of medical devices to ensure they meet the highest standards of safety and efficacy.
- Collaboration: Excellent communication and teamwork skills, with the ability to work effectively across departments and with external partners.
- Innovation-Driven: Passion for medical technology innovation, with a desire to push the boundaries of ECG device capabilities to improve patient outcomes.
- Education: A bachelor’s or master’s degree in biomedical engineering, electrical engineering, or a related field is required. Advanced degrees or certifications in medical device design or regulatory affairs are a plus.
Tell employers what skills you have
Usability
CE marking
Leadership
FDA
Quality Control
Regulatory Affairs
ISO
Biomedical Engineering
Attention to Detail
Medical Devices
Regulatory Requirements
Teamwork Skills
Regulatory Submissions
Electrical Engineering
Japanese
Signal Processing
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