Job description- System Integrator At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector. Responsibilities: Define, refine, and maintain system architecture across multiple medical devices. Identify and document critical subsystems, their interdependencies, and system integration complexity. Create and maintain system block diagrams, interface control documents (ICDs), and control/data flowcharts. Decompose product requirements into core working principles and coordinate engineering solutions around them. Ensure coherence in product function, behavior, and user experience. Conduct early design feasibility assessments to identify critical components that determine system feasibility Map critical development paths, including components with long lead times, dependency risks, and integration constraints. Proactively flag dependencies that can delay product readiness and escalate mitigation strategies. Lead the technical integration of mechanical, electronic, firmware, and industrial design subsystems. Coordinate to define tolerances, mounting constraints, connector selection, and interface sealing as per product use case. Lead system-level DFMEA/ PFMEA, including interface-level failure modes Collaborate with V&V to map requirements to test cases, ensuring test coverage for integrated systems. Actively support prototype building and test bench development and debug integration-related during testing. Own the integration readiness checklist for each product milestone. Ensure all system-level documentation complies with ISO 13485, ISO 14971, IEC 60601, IEC 62304, and usability norms. Coordinate deliverables with mechanical, electronics, embedded, V&V, usability, and regulatory teams. Provide regular technical status updates to the Project Manager, including risk flags, component delays, and dependency shifts. Work closely with the Project Manager to support deliverable tracking, timeline reviews, and milestone readiness. Qualifications: Bachelor’s or Master’s degree in Mechanical, Electronics, Mechatronics, or Biomedical Engineering. 4+ years of experience in medical device product development. Must have led the end-to-end development and integration of at least two medical devices. Proven hands-on experience in at least one core domain (e.g., mechanical, electronics, embedded systems, or software), along with a sound understanding of other domains to enable effective cross-functional collaboration and technical integration. Exposure to design for manufacturing (DFM/DFA), sterilization compatibility, and design controls under ISO 13485. Systems thinking and deep attention to cross-domain interactions. Proactive communicator and integrator across technical functions. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide! Show more Show less

As an Electronics Assembly Engineer at IF MedTech, you will play a crucial role in ensuring the flawless assembly and unit testing of medical devices with electrical and electromechanical subsystems. Your responsibilities will include assembling electronic components, PCBs, and wiring based on engineering schematics, conducting functional testing and troubleshooting to guarantee optimal performance, and identifying and rectifying defects in the assembly processes in collaboration with design and quality assurance teams. You will oversee the operation of soldering stations, rework stations, and automated assembly equipment, while maintaining comprehensive documentation of assembly procedures, test results, and quality control measures. In this role, you will need to ensure compliance with industry standards such as IPC, ISO, and safety regulations, as well as collaborate with cross-functional teams to enhance assembly techniques and verify incoming components from vendors. Your commitment to quality and compliance, along with a focus on first-time-right production, will be essential in meeting daily production goals and resolving non-conformities through rework, segregation, and in-house repairs. Additionally, you will be responsible for implementing safety practices and maintaining workplace discipline in accordance with 5S and PPE protocols. To qualify for this position, you should hold a Diploma in Electronics Engineering and possess at least 2-4 years of experience in electrical or electromechanical assembly, preferably in the medical device or other regulated industries. A strong knowledge of basic electrical testing tools, familiarity with IPC standards, ISO 13485 documentation, and good manufacturing practices, as well as the ability to read and interpret circuit diagrams and assembly drawings, are required. Excellent problem-solving, coordination, and documentation skills, along with the ability to work collaboratively in cross-functional teams and a good understanding of best manufacturing practices, will be key to your success in this role. Awareness of housekeeping, 5S activities, and the use of personal protective equipment (PPEs) will also be expected.,

Tips: Provide a summary of the role, what success in the position looks like, and how this role fits into the organization overall. Responsibilities This is an on-site role for an PCB Design Engineer. The PCB Design engineer will be responsible for designing printed circuit boards (PCB) for various electronic medical devices, communicating with team members about design specifications, collaborating with cross-functional teams to identify solutions, and providing technical support related to PCB design as needed. This position requires a keen understanding of medical device regulations, precision in design, and collaboration with multidisciplinary teams to create innovative and reliable solutions. PCB Design and Development: Create, design, and optimize PCB layouts, schematics, and structures tailored specifically for medical devices, adhering to industry standards and regulatory requirements. Implement best practices in PCB layout design, considering factors like signal integrity, thermal management, electromagnetic compatibility, and manufacturability. Regulatory Compliance: Ensure all PCB designs comply with relevant medical device regulations, such as IEC 60601 and ISO 13485, as well as country-specific regulatory standards (FDA, CE, etc.). Maintain awareness of evolving regulatory guidelines and update designs accordingly to ensure continued compliance. Collaboration and Communication: Work closely with cross-functional teams including hardware engineers, embedded systems engineers, mechanical engineers, and product designers to understand project requirements and contribute to the overall system design. Effectively communicate design concepts, constraints, and technical details to team members and stakeholders. Component Selection and Integration: Identify and select appropriate electronic components for PCB designs, considering performance, reliability, and compatibility with medical device requirements. Collaborate with vendors and suppliers to source components and ensure their seamless integration into the PCB design. Prototyping and Testing Support: Assist in the fabrication of PCB prototypes, support testing procedures, and participate in validation activities to verify the functionality and performance of the PCB designs. Troubleshoot and address any design-related issues during prototype testing. Documentation and Reporting: Prepare detailed documentation, including schematic diagrams, technical specifications, bill of materials (BOM), design verification reports, and assembly instructions. Maintain accurate records and documentation for design revisions and changes throughout the development lifecycle. Disseminate knowledge and good practices through courses, events, demos, visits, and exhibitions. Note: The responsibilities and qualifications outlined above are indicative and may vary depending on the specific needs of the employing organization and the complexity of the medical devices being developed. Qualifications Expertise in using various software required for PCB design such as Altium Designer, Eagle, or similar Proficiency in designing multi-layer PCBs according to design specifications and ensuring design quality Experience with generating design rules, Gerber files for PCB fabrication, and assembly files for PCB assembly Ability to collaborate with hardware, mechanical, and software teams and communicate technical requirements for PCB design. Good understanding of PCB manufacturing processes, assembly processes, and testing methodology Bachelor's degree or higher in Electrical or Electronics Engineering, or a related field 2+ years of experience in PCB design In-depth knowledge of medical device regulations, particularly IEC 60601 and ISO 13485. Strong understanding of PCB layout principles, signal integrity, EMI/EMC considerations, and thermal management. Excellent verbal and written communication skills, and ability to work effectively in cross-functional teams and with management. Experience with product development life cycle, design control processes, and product documentation is a plus

About us: At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector. Responsibilities: ● Design multi-layer PCBs for medical devices, ensuring optimal performance, reliability, and manufacturability. ● Create and optimize schematics and PCB layouts using industry-standard design tools (e.g., Altium, Eagle, Or CAD). ● Integrate hardware components such as microcontrollers, sensors, power supplies, communication interfaces, and other embedded system components. ● Work closely with embedded engineers to define system requirements and ensure smooth hardware- software integration. ● Collaborate with manufacturing teams to ensure design-for-manufacturing (DFM) principles are applied and designs can be scaled for production. ● Interface with component suppliers to select optimal parts, ensuring cost-effectiveness and availability. ● Develop and test PCB prototypes to ensure performance aligns with product specifications. ● Perform hardware debugging and troubleshooting to resolve design issues and optimize system performance. ● Conduct failure analysis, root cause analysis, and component selection reviews to enhance hardware reliability. ● Ensure designs meet medical device safety and regulatory standards, including ISO 13485, IEC 60601, and other relevant guidelines. ● Maintain comprehensive design documentation, including schematics, layout files, Bill of Materials (BOM), and technical reports. ● Contribute to risk management, FMEA, and validation processes to ensure product safety and quality. ● Optimize hardware designs for power consumption, signal integrity, EMI/EMC performance, and thermal management. ● Stay updated with the latest advancements in PCB technologies, materials, and industry best practices. ● Participate in peer reviews and provide constructive feedback to enhance team-wide design quality. Qualifications: ● Bachelor's degree in Electrical Engineering, Electronics, or a related field. ● Minimum 2 years of experience in PCB design, specifically in high-reliability or regulated industries (medical devices preferred). ● Proficiency with PCB design tools such as Altium Designer, Eagle, OrCAD, or KiCad. ● Experience with high-speed digital, analog, and mixed-signal PCB designs. ● Knowledge of EMI/EMC design considerations, signal integrity, power integrity, and thermal management. ● Familiarity with hardware communication protocols such as UART, SPI, I2C, and CAN. ● Understanding of safety and regulatory requirements for medical devices (e.g., ISO 13485, IEC 60601, FDA, etc.).Strong communication and teamwork skills. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!

Job description At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector. Responsibilities ● Create initial concept sketches and product visualizations ● Develop and present multiple early-stage design directions to stakeholders ● Translate user needs and product requirements into aesthetic and ergonomic product solutions ● Collaborate with engineering teams to align form with function ● Integrate feedback from mechanical, electronics, and user research into design iterations ● Create product architecture across multiple medical devices. ● Resolve cross-functional challenges through collaborative design thinking ● Develop detailed industrial design outputs, including CMF (Color, Material, Finish) specifications ● Define final product geometry, part splits, material selections, and finishing details ● Ensure alignment with design for manufacturing (DFM) and design for assembly (DFA) principles ● Select appropriate prototyping methods and build physical and digital prototypes ● Plan and implement structured prototype feedback sessions ● Collect, analyze, and incorporate feedback into design refinements ● Validate and test design iterations with internal and external stakeholders ● Promote knowledge sharing and best practices through internal training, demos, and participation in external industry events. Qualifications ● Master’s degree in Industrial Design (preferred) ● Strong skills in concept generation, rendering, and CAD modeling (SolidWorks, Illustrator, Photoshop) ● Experience in DFM/DFA, usability design, and electromechanical product development ● Familiarity with ISO 13485 and medical device development context ● Ability to manage cross-functional collaboration and iterative workflows ● Proactive communicator and integrator across technical functions. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!

About the job At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector. Responsibilities ● Develop and execute verification and validation protocols for medical device hardware and associated mobile and web applications. ● Design and set up testing environments for hardware and software components of medical devices. ● Perform functional, performance, and usability testing for software and hardware components. ● Identify and document defects and inconsistencies, collaborating with development teams for resolution. ● Design, implement, and execute automated test scripts for software applications where applicable. ● Assist in defining test strategies, test plans, and acceptance criteria for hardware and software systems. ● Ensure compliance with industry regulations such as ISO 13485, IEC 62304, and FDA guidelines. ● Contribute to the preparation of detailed test reports and validation documentation. ● Maintain testing tools and environments, ensuring readiness and calibration. ● Provide inputs for risk assessment and design reviews during product development. ● Maintain testing tools and equipment, ensuring calibration and readiness for testing. ● Stay updated with advancements in testing tools, automation frameworks, and industry best practices. Qualifications ● Bachelor's degree in Biomedical Engineering, Computer Science, Electronics, or a related field. ● Preferably 0 to 2 years of experience in verification, validation, or quality testing, preferably in the medical device or software development domain. ● Ability to design and implement testing setups for hardware and software. ● Knowledge of industry standards such as ISO 13485, IEC 60601, IEC 62304, and FDA guidelines. ● Experience with documentation for regulatory submissions is advantageous. ● Familiarity with automated testing tools like Selenium, Appium, or similar frameworks is preferred. ● Proficiency in defect tracking tools (e.g., JIRA) and version control systems (e.g., Git). ● Strong analytical, problem-solving, and attention-to-detail skills. ● Excellent documentation and communication skills. ● A collaborative mindset with a proactive approach to problem-solving. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!

Job description At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector. Responsibilities ● Design, develop, and debug embedded software for various hardware platforms, including microcontrollers and processors. ● Troubleshoot and resolve electronics design issues, including hardware-level debugging. ● Write and optimize efficient embedded C/C++ code tailored for real-time systems and low-power environments. ● Collaborate with hardware engineers to define system architecture, specifications, and integration requirements. ● Develop firmware, drivers, and hardware-software interfaces. ● Perform system integration, testing, and troubleshooting for embedded systems. ● Implement and debug communication protocols such as UART, SPI, I2C, CAN, and Ethernet. ● Optimize system performance, focusing on memory, power consumption, and CPU efficiency. ● Ensure adherence to industry standards (including ISO 13485) and safety regulations for medical device development. ● Maintain detailed technical documentation for system architecture, designs, and code. ● Participate in code reviews, providing and receiving constructive feedback for continuous improvement. ● Collaborate with QA teams to develop and execute comprehensive test plans for hardware and software validation. ● Promote knowledge sharing and best practices through internal training, demos, and participation in external industry events. Qualifications ● Bachelor's degree in Electrical Engineering, Electronics, or a related field. ● 3+ years of experience (other candidates with relevant projects (medical device) may apply) ● Proficiency in C, C++, Embedded C, and Assembly is a plus, with familiarity in assembly language. ● Experience with microcontrollers, ARM Cortex, and other embedded platforms. ● Experience with IoT, Wireless Communication (BLE, Wi-Fi), or AI/ML in embedded systems is a plus ● Proficiency with real-time operating systems (RTOS) and debugging tools like JTAG. ● Strong understanding of hardware schematics, PCB layouts, and hardware-software interaction. ● Familiarity with version control systems such as Git. - Knowledge of hardware communication protocols like SPI, I2C, UART, CAN, etc. - Excellent problem-solving and debugging skills. ● A collaborative mindset and willingness to work in a fast-paced, innovative environment. ● Experience in medical devices is a plus, but not mandatory ● Should be aware of the ISO 13485-work environment. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!

At IF MedTech, we are dedicated to revolutionizing healthcare through cutting-edge medical device design, development, and pilot manufacturing. Our global team collaborates with experts across medical, engineering, business, and research domains to bring innovative solutions that enhance healthcare and improve lives. Join us in our mission to drive innovation and make a global impact in the medical technology sector. As a Procurement & Vendor Management professional at IF MedTech, your responsibilities will include sourcing and negotiating with suppliers for quality materials and best pricing. You will be expected to maintain strong relationships with existing vendors while also identifying new suppliers. Ensuring timely procurement of raw materials, equipment, and services will be a key part of your role. In terms of Purchase Order & Documentation, you will be responsible for preparing and issuing Purchase Orders (PO) based on approved requisitions. It will be essential to maintain accurate procurement records, invoices, and supplier contracts while ensuring compliance with company policies and procurement standards. Your role will also involve Inventory & Supply Chain Coordination, where you will work closely with warehouse and logistics teams to manage stock levels effectively. Monitoring inventory to prevent shortages or overstocking, as well as coordinating with internal departments to ensure a smooth workflow, will be crucial aspects of your responsibilities. To qualify for this position, you should hold a Bachelor's degree in Commerce and have 1-2 years of experience in procurement, purchasing, or supply chain roles. Proficiency in MS Office (Excel, Word) is a requirement for this role. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!,