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!,
Job Summary: As a Mechanical Design Engineer, you will contribute to the design, development, and testing of innovative medical devices in compliance with ISO 13485 and regulatory standards. You will support the design team with concept generation, prototyping, and ensuring the manufacturability and reliability of devices. Responsibilities: Assist in concept generation, detailed design, and prototyping of medical devices. Perform 3D CAD modeling, drafting, and engineering calculations to ensure product performance and reliability. Collaborate with cross-functional teams to meet product specifications, performance, and compliance requirements. Conduct design feasibility studies and support risk assessments for mechanical components. Assist in testing and validation activities, including preparation of test protocols and analysis of results. Perform Design for Manufacturing (DFM) and Design for Assembly (DFA) efforts to streamline production. Release the designs for production purposes. Coordinate with the production team for smooth transfer of designs to the production floor, prepare necessary documents for the production purposes. Work with suppliers and vendors to source materials and components. Coordinate with vendors for small batch manufacturing, customized components manufacturing. Participate in internal design reviews and support documentation for regulatory submissions. Stay updated with industry trends, materials, and manufacturing processes relevant to medical devices. Skills Required: Proficiency in CAD software (e.g., SolidWorks, AutoCAD), GD&T, Tolerance Analysis, Engineering design. Basic understanding of materials science and manufacturing processes. Familiarity with ISO 13485 and basic regulatory compliance standards. Analytical skills for problem-solving and design optimization. Strong communication and teamwork abilities. Attention to detail and a commitment to quality assurance. Educational Qualifications: Bachelor’s degree in Mechanical Engineering or a related field with 3+ years of experience in product design and manufacturing.
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, review, and maintain Clinical Evaluation Plans (CEPs) and Clinical Evaluation Reports (CERs) in line with EU MDR, MEDDEV 2.7/1 Rev. 4, and relevant MDCG guidance documents. Conduct systematic literature reviews and clinical data analysis Update CERs based on findings from Post-Market Surveillance (PMS), Post-Market Clinical Follow-up (PMCF) studies, and risk management files. Collaborate with clinical, design, and risk management teams to gather relevant inputs. Prepare and maintain PMS Plans, PMS Reports, and PMCF Plans/Reports. Develop and update Periodic Safety Update Reports (PSURs) and Summaries of Safety and Clinical Performance (SSCPs). Analyze complaint data, adverse events, and other real-world evidence to detect trends or emerging risks. Coordinate vigilance reporting and Field Safety Corrective Actions (FSCAs). Review and verify device labels and packaging artwork for compliance with EU MDR, FDA, ISO 15223-1, ISO 20417, and other applicable standards. Ensure correct inclusion of symbols, warnings, contraindications, and UDI information. Update and maintain Instructions for Use (IFUs) in alignment with CER, risk files, and usability findings. Support labelling translations and ensure adherence to country-specific labelling requirements. Lead or support CAPA initiation, investigation, root cause analysis, and closure for product quality or regulatory compliance issues. Work with Quality Assurance and Engineering teams to define and verify corrective/preventive actions. Track CAPA timelines and ensure documentation is in accordance with ISO 13485 requirements. Participate in continuous improvement initiatives from audit findings, PMS insights, and internal reviews. Qualifications Bachelor’s or Master’s degree in Biomedical Engineering, Life Sciences, Pharmacy, or related discipline. 3–6 years in Regulatory Affairs within the medical device industry. Proven track record in CERs, PMS, device labelling, and CAPA management. Strong knowledge of EU MDR 2017/745, ISO 13485, ISO 14971, MEDDEV 2.7/1 Rev. 4, and related regulations/standards. Proficiency in literature search tools (PubMed, Embase). Strong technical writing and documentation skills for regulatory submissions. Excellent analytical and problem-solving abilities. Strong interpersonal and cross-functional collaboration skills. Ability to manage multiple priorities under regulatory timelines.
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 optimize Android-native components using Java/Kotlin. ● Collaborate with the Flutter developer to integrate Android modules into cross-platform builds. ● Ensure secure data handling, storage, and permissions in compliance with HIPAA. ● Support responsive and accessible UI integration for mobile and web interfaces. ● Design, develop, and maintain backend services using Python FastAPI and Java. ● Implement RESTful and GraphQL APIs for seamless data flow between devices, apps, and servers. ● Apply Java frameworks such as Spring Boot where applicable for service development. ● Optimize backend services for high-volume, low-latency medical data processing. ● Work with relational databases (PostgreSQL, MySQL) and NoSQL databases (MongoDB). ● Design efficient schemas and implement secure data access patterns. ● Ensure database architecture supports scalability, redundancy, and compliance. ● Deploy and manage applications on AWS (EC2, S3, RDS, Lambda, API Gateway, etc.). ● Set up CI/CD pipelines for automated build, test, and deployment. ● Use Docker for containerization and reproducible environments. ● Monitor and optimize cloud resource usage for cost efficiency. ● Adhere to ISO 13485 and HIPAA standards for medical software development. ● Participate in code reviews, unit testing, and automated quality checks. ● Maintain proper documentation as per medical device software lifecycle requirements. Qualifications: ● Bachelor’s degree in Computer Science, Software Engineering, or a related field. ● Experience: 2–4 years in full-stack development with proven backend and Android expertise. ● Must-have: Proficiency in Java for Android and backend services. ● Plus: Knowledge of Spring/Spring Boot. ● Strong in Python (FastAPI). ● Proficiency in AWS services and deployment pipelines. ● Experience with relational and NoSQL databases. ● Familiarity with HIPAA and ISO 13485 guidelines. ● Hands-on with Git, Docker, CI/CD workflows. ● Ability to work independently and collaborate effectively. ● Strong problem-solving, adaptability, and attention to detail. Join IF MedTech to drive innovation in healthcare technology and develop software solutions that transform lives worldwide!
Job Title: Operations Officer - Prototyping Job Summary The Operations Officer - Prototyping will work closely with the design and development teams to support the realization of innovative medical device prototypes. This role involves hands-on fabrication, coordination with external vendors, maintenance of internal prototyping equipment, and ensuring that prototypes are developed efficiently and meet specified technical and quality standards in line with requirements. Responsibilities Collaborate with engineers and designers to understand prototype requirements and specifications. Fabricate and assemble prototypes using various manufacturing methods (e.g., 3D printing, machining, manual assembly). Operate, maintain, and calibrate internal prototyping equipment including 3D printers, Equipments, machines, laser cutters, etc. Source materials, tools, and components necessary for prototype fabrication. Coordinate with external vendors for specialized fabrication, machining, and procurement activities. Manage prototype build schedules to align with overall project timelines. Document prototype fabrication processes, modifications, and testing results accurately. Support design verification and validation activities through prototype testing assistance. Ensure compliance with internal SOPs and quality system requirements (ISO 13485). Implement improvements in prototype processes to enhance quality, speed, and cost-effectiveness. Maintain a safe, organized, and efficient prototyping lab environment. Skills Required Strong hands-on skills in mechanical fabrication, assembly, and troubleshooting. Proficiency in operating prototyping and fabrication equipment (e.g., hand tools). Basic understanding of mechanical and electrical systems related to medical devices. Familiarity with reading and interpreting engineering drawings and schematics. Vendor management and material sourcing skills. Basic knowledge of design for manufacturability (DFM) and prototyping best practices. Good documentation and reporting abilities. Effective communication and teamwork skills. Ability to work independently under minimal supervision. Awareness of medical device development regulatory and quality standards (ISO 13485) is an advantage. Educational Qualifications Diploma in Mechanical Engineering, Biomedical Engineering, Industrial Design, or a related technical field. Certification or technical training in fabrication, machining, or prototyping techniques is a plus. Experience 4+ years of hands-on experience in a prototyping, fabrication, or technician role. Prior experience in the medical device industry or a regulated industry is highly desirable.
As an Operations Officer - Prototyping, you will collaborate closely with the design and development teams to support the realization of innovative medical device prototypes. Your role will involve hands-on fabrication, coordination with external vendors, maintenance of internal prototyping equipment, and ensuring that prototypes are developed efficiently to meet specified technical and quality standards as per requirements. You will work with engineers and designers to understand prototype requirements and specifications. Fabricating and assembling prototypes using various manufacturing methods such as 3D printing, machining, and manual assembly will be part of your responsibilities. Operating, maintaining, and calibrating internal prototyping equipment like 3D printers, machines, and laser cutters will also be essential. In addition, you will be responsible for sourcing materials, tools, and components required for prototype fabrication. Coordinating with external vendors for specialized fabrication, machining, and procurement activities, managing prototype build schedules, and documenting prototype fabrication processes and testing results accurately are crucial tasks in this role. Your skills in mechanical fabrication, assembly, and troubleshooting will be essential, along with proficiency in operating prototyping and fabrication equipment. A basic understanding of mechanical and electrical systems related to medical devices, the ability to read and interpret engineering drawings and schematics, and vendor management and material sourcing skills are required. Moreover, you should have knowledge of design for manufacturability (DFM) and prototyping best practices, good documentation and reporting abilities, effective communication and teamwork skills, and the ability to work independently under minimal supervision. Awareness of medical device development regulatory and quality standards, particularly ISO 13485, would be advantageous. Ideally, you should hold a Diploma in Mechanical Engineering, Biomedical Engineering, Industrial Design, or a related technical field. Certification or technical training in fabrication, machining, or prototyping techniques would be a plus. With at least 4 years of hands-on experience in a prototyping, fabrication, or technician role, prior experience in the medical device industry or a regulated industry is highly desirable. Overall, your role as an Operations Officer - Prototyping will be pivotal in ensuring the successful development of high-quality medical device prototypes through effective collaboration, meticulous fabrication, and adherence to technical and quality standards.,
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 ● Manage end-to-end recruitment processes, including sourcing, interviewing, and onboarding new talent. ● Handle employee relations, performance management, and ensure adherence to company policies and regulations. ● Develop and execute social media strategies to enhance the company's employer brand across platforms such as LinkedIn, Twitter, Instagram, and others. ● Create engaging content for social media channels, highlighting company culture, employee achievements, and job opportunities. ● Manage employee engagement programs and internal communications through social media channels. ● Organize and manage employee training and development programs. ● Coordinate and manage company-wide travel arrangements, ensuring cost-effective and seamless travel plans for employees and management. ● Plan, coordinate, and host internal and external events, including conferences, team-building activities, and company celebrations. ● Develop and implement HR processes and systems for efficient employee management, record-keeping, and compliance. ● Create scalable processes for recruitment, onboarding, training, and employee development. ● Maintain accurate HR records and ensure compliance with labor laws and regulations. Qualifications ● Bachelor's degree in Human Resources, Business Administration, or a related field. ● 3+ years of experience in human resources, with a strong focus on recruitment and employee engagement. ● Proven experience in managing social media channels and creating content for professional platforms. ● Experience in coordinating travel and managing event logistics. ● Strong understanding of social media analytics and tools to measure campaign success. ● Excellent communication and interpersonal skills. ● Ability to multitask and manage priorities in a fast-paced environment. ● Familiarity with HR software and tools (e.g., Zoho Recruit). ● Experience in organizing events and creating HR systems and processes. ● Passion for building and maintaining a strong company culture.
Job Description As a Printed Circuit Board Designer at IF MedTech, you will play a crucial role in creating detailed PCB layouts, selecting appropriate components, and designing circuit boards for various applications. Your responsibilities will also include ensuring compliance with manufacturing standards and working closely with engineering and production teams to develop and optimize designs. To excel in this role, you should have experience in Circuit Design, Hardware, Electronics, and Electrical Engineering. Proficiency with PCB design software and tools is essential, along with strong problem-solving and analytical skills. Your ability to collaborate effectively with cross-functional teams will be key in contributing to our innovative medical device design and development projects. You will be based in Navi Mumbai and will be an integral part of our global team that is dedicated to revolutionizing healthcare and making a positive impact in the medical technology sector. If you have a Bachelor's degree in Electrical Engineering, Electronics Engineering, or a related field, along with attention to detail and a commitment to quality, we invite you to join us in our mission to drive innovation and improve lives.,
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. ● 4+ 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!
You will be responsible for designing multi-layer PCBs for medical devices at IF MedTech, ensuring optimal performance, reliability, and manufacturability. Your role will involve creating and optimizing schematics and PCB layouts using industry-standard design tools like Altium, Eagle, or OrCAD. Additionally, you will integrate hardware components such as microcontrollers, sensors, power supplies, communication interfaces, and other embedded system components. Collaboration with embedded engineers to define system requirements and ensure smooth hardware-software integration will be a key aspect of your job. You will also work closely with manufacturing teams to apply design-for-manufacturing (DFM) principles and ensure that designs can be scaled for production. Interface with component suppliers will be required to select optimal parts in terms of cost-effectiveness and availability. Your responsibilities will also include developing and testing PCB prototypes, performing hardware debugging and troubleshooting, conducting failure analysis, and root cause analysis to enhance hardware reliability. It will be essential to ensure that designs meet medical device safety and regulatory standards like ISO 13485, IEC 60601, and other relevant guidelines. Maintaining comprehensive design documentation, contributing to risk management, FMEA, and validation processes, and optimizing hardware designs for power consumption, signal integrity, EMI/EMC performance, and thermal management are crucial aspects of the role. Staying updated with the latest advancements in PCB technologies, materials, and industry best practices, as well as participating in peer reviews to provide constructive feedback for enhancing team-wide design quality, will be expected. Qualifications required for this position include a Bachelor's degree in Electrical Engineering, Electronics, or a related field, along with 4+ years of experience in PCB design, preferably with exposure to medical device development. Proficiency in PCB design tools such as Altium Designer, Eagle, or OrCAD is essential, as well as familiarity with high-speed digital, analog, and mixed-signal PCB designs. Knowledge of EMI/EMC, signal integrity, thermal management in PCB design, medical device regulatory standards, and hardware communication protocols like UART, SPI, I2C, or CAN is also necessary. Excellent communication and teamwork skills, coupled with a strong problem-solving attitude, are qualities that will be beneficial in this role.,