136 Biomedical Engineering Jobs

Planning Scheduling and Implementing Planned Preventive Maintenance program, as per Sodexo CTM guidelines, using CMMS minuteman Implementing Corrective Maintenance including routine corrective maintenance, breakdown and emergency maintenance. Adhere to agreed Response Time and Turn-around time. Ensure that service reports are properly filed, to maintain high quality of documentation Ensure that purchase requisitions for spare parts are properly filed Carry out all acceptance tests according to guidelines from the manufacturer Carry out Performance Testing and Electrical Safety Testing Ensure that all regulatory requirements are fulfilled Prepare contingency plan Perform and maintain calibration report, participate in the audits Use appropriate personnel protective equipment (PPE) while servicing the equipment Follow appropriate Decontamination procedure Maintain appropriate record of Incidents and Hazards Plan, schedule and conduct User Trainings Maintain adequate stock of spare parts Generate reports from CMMS, as required Carry out administrative, finance and HR responsibilities as required

Planning Scheduling and Implementing Planned Preventive Maintenance program, as per Sodexo CTM guidelines, using CMMS minuteman Implementing Corrective Maintenance including routine corrective maintenance, breakdown and emergency maintenance. Adhere to agreed Response Time and Turn-around time. Ensure that service reports are properly filed, to maintain high quality of documentation Ensure that purchase requisitions for spare parts are properly filed Carry out all acceptance tests according to guidelines from the manufacturer Carry out Performance Testing and Electrical Safety Testing Ensure that all regulatory requirements are fulfilled Prepare contingency plan Perform and maintain calibration report, participate in the audits Use appropriate personnel protective equipment (PPE) while servicing the equipment Follow appropriate Decontamination procedure Maintain appropriate record of Incidents and Hazards Plan, schedule and conduct User Trainings Maintain adequate stock of spare parts Generate reports from CMMS, as required Carry out administrative, finance and HR responsibilities as required

As a skilled Biomedical Engineer specializing in device integration, you will be responsible for leading the integration of biomedical devices with our Hospital Information System (HIS) and Electronic Medical Records (EMR) at Medanta, Gurgaon. Your expertise in bio medical devices and their interoperability via HL7, PHIR, and RESTful API integration will be crucial in ensuring seamless data flow between medical devices and hospital systems. This integration is essential for enhancing real-time patient record availability, revenue assurance, operational efficiency, and clinical decision-making. At Medanta, a forward-thinking healthcare organization at the forefront of digital innovation, you will play a pivotal role in automating medical devices to improve EMR effectiveness, clinical efficiency, and patient outcomes. Your key responsibilities will include leading the integration of various biomedical devices such as radiology machines, point-of-care testing devices, lab machines, heart stations, endoscopy/colonoscopy units, OT & ICU equipment with HIS/EMR. You will develop and implement device communication protocols using PHIR, HL7, and RESTful APIs, working closely with vendors, IT teams, and clinicians to ensure a smooth integration process. Additionally, you will establish data exchange workflows between biomedical devices and hospital IT systems, ensuring data accuracy, security, and compliance with regulatory standards. Your role will involve troubleshooting and resolving integration-related technical issues, supporting software upgrades, patches, and device firmware updates. To enhance clinical and operational efficiency, you will enable real-time patient data availability, develop and maintain clinical dashboards for real-time monitoring and decision support, and ensure integration supports automated alerts and notifications for critical patient values. Collaboration with clinical, IT, and finance teams will be essential to ensure seamless revenue cycle management. Vendor and stakeholder management will also be a part of your responsibilities, including evaluating and working with biomedical device manufacturers, middleware providers, and software vendors. You will document and maintain integration protocols, troubleshooting guides, and training materials to support the integration process effectively. To qualify for this role, you should have a Bachelors/Masters degree in Biomedical Engineering, Electronics & Instrumentation, or a related field. Technical expertise in integrating biomedical devices with HIS/EMR, hands-on experience with HL7, DICOM, PHIR, and RESTful APIs, as well as knowledge of device connectivity standards and protocols are essential. Preferred experience includes 7-10 years in a hospital, healthcare IT, or medical device industry, familiarity with regulatory standards, and strong problem-solving, communication, and collaboration skills. Join us at Medanta, where you will have the opportunity to make a significant impact on healthcare automation and patient outcomes through innovative device integration solutions.,

As an Industry Analyst at APIFDF Analytics in Ahmedabad, Gujarat, India, you will be an integral part of the leading provider of global supply chain intelligence solutions for the pharmaceutical industry. With a focus on end-to-end visibility and in-depth market analyses, you will work alongside a dedicated team of industry analysts, IT professionals, and software engineers to deliver customized analytics solutions to clients across various industries. Your primary responsibility will involve conducting comprehensive market research across pharmaceuticals, chemicals, food, and medical devices sectors. By analyzing trends, competition, and consumer behavior, you will generate actionable insights to support strategic decision-making. Additionally, you will maintain a robust industry intelligence database, engage with potential clients, and collaborate with sales and IT teams to ensure alignment between market insights and business goals. Key Responsibilities: - Research domain knowledge, industry trends, customer needs, and competitors. - Analyze data to generate insights and recommendations. - Identify and engage potential clients for research purposes. - Maintain a market intelligence database. - Align sales strategies with internal teams. - Track performance using KPIs. - Monitor industry trends for opportunities and risks. - Present insights and recommendations to stakeholders. To excel in this role, you should possess a Bachelor's degree in chemistry, pharmaceuticals, biochemistry, biotechnology, food technology, or biomedical engineering (Master's degree preferred). With 0-2 years of experience, proficiency in tools like Excel, PowerPoint, and Email is essential. Strong written and verbal communication skills, analytical thinking abilities, and a self-motivated approach are key attributes for success in this position. Additionally, familiarity with business analytics software and data visualization tools is advantageous. Join us at APIFDF Analytics to enjoy a competitive compensation and benefits package, ranging from 3,00,000 to 4,50,000. You will have the opportunity to contribute to an innovative company that is making a meaningful impact in various industries, work with a passionate and collaborative team, and access career growth opportunities through training and professional development.,

What We Want You To Do Approve new equipment through testing, ensuring standards and compliance Install new equipment by setting, adjusting, calibrating, and testing functionality Maintain equipment by following preventive maintenance schedules, performing tests, troubleshooting, and resolving malfunctions Calls for special equipment service, evaluates service contracts and maintains equipment inventories. Directs biomedical equipment operation by providing equipment operation demonstrations, instructing other staff in use and care of equipment and answering questions. Evaluates proposed equipment by conducting tests and evaluations. Maintains supplies inventory by checking stock, anticipating needs, placing and expediting orders, and verifying receipt. Compile, analyze, and summarize data to prepare biomedical reports, highlighting information and trends Write reports and documents describing protocols, policies, maintenance, standards for use and repair of biomedical tools, machinery, and software Requirements Proven work experience in biomedical equipment quality control and quality assurance. Have an understanding of quality control, quality assurance and quality checks. Awareness of ISO 15189 and ISO 13485 & other regulatory requirements. Skills Keen attention to details. Ability to critically evaluate the requirements of the relevant ISO standards.. Ability to work independently with minimal supervision as well as collaboratively in a team environment. Strong analytical and problem-solving abilities. Ability to execute tasks and document information independently. Excellent organizational and time management skills with the ability to prioritize tasks effectively Strong interpersonal and communication skills with the ability to interact professionally with diverse stakeholders Skills : problem-solving abilities , genomics , organizational skills,quality control,iso 13485,analytical skills,communication skills,time management,iso,iso 15189,keen attention to details,interpersonal skills,quality assurance

Cyrix health care is currently seeking a Sales Executive to join our team. As a Sales Executive, you will be responsible for conducting sales activities within the assigned territories in Kerala. You will also be in charge of providing services within the same territories, keeping a regular check on the present stock, offering information for billing items, and ensuring effective communication for items to be purchased for further selling. The ideal candidate should have a Degree or Diploma in biomedical engineering and a proven track record as a Sales and Service Representative. A minimum of 2 years of work experience in sales, preferably in lab equipment's, is required. Additionally, proficiency in MS Office, excellent selling, negotiation, and communication skills, as well as strong prioritizing, time management, and organizational abilities are essential for this role. The position is based in Karnataka and the working schedule is full-time for fresher candidates. The work hours are during the day shift and proficiency in English is preferred. The successful candidate will be expected to work in person at the designated work location. To apply for this position, please send your resume to career@cyrix.in or contact us at 9744400633. We look forward to welcoming a dedicated and enthusiastic individual to our team at Cyrix health care.,

Applications are now open for the Master of Digital Health (MDH) program at Deggendorf Institute of Technology in Germany. This innovative program is designed for future leaders in digital transformation within health and wellness sectors, offering a unique interdisciplinary, international, and innovative curriculum. The instruction is fully conducted in English, making it accessible to a global audience. An attractive feature of this program is that there are no tuition fees for international students, providing an opportunity for individuals from various backgrounds to participate. The program is open to graduates from biomedical and technical disciplines, fostering a diverse learning environment. Deggendorf Institute of Technology is proud to be one of only six WHO Collaborating Centers on Digital Health, highlighting its expertise and commitment to advancing digital health initiatives. Additionally, the institute hosts the global DigiHealthDay Forum & Series, providing students with valuable networking opportunities and exposure to the latest trends in digital health. Situated in Germany, recognized as Europe's Digital Health Innovation Hub, students will benefit from being in a leading environment for digital health research and development. With over 1,800 applicants last year, the program has garnered significant interest from prospective students worldwide. To be eligible for the Master of Digital Health program, applicants must hold a degree in biomedical, technical, or related fields. The application deadline is July 15, 2025. Interested candidates are encouraged to apply through the official website: https://th-deg.de/dh-m-en. This program offers a unique chance to join a globally recognized graduate program at the forefront of digital health, equipping students with the skills and knowledge needed to drive innovation in the healthcare industry. For more opportunities in your field and preferred country, you can sign up for a 14-day free trial to receive job alerts straight to your email inbox: https://phdfinder.com/position-alert-service/ We are an independent team dedicated to helping students find valuable opportunities. If you found this information helpful, consider supporting us with a coffee.,

You specialize in providing acute neuromonitoring services, focusing on continuous monitoring of patients" neurological functions during critical periods like neurosurgeries and acute neurological conditions. The main goal is to detect any changes in neurological status promptly to allow for timely interventions and management. As an Intraoperative Neuromonitorist based in Bengaluru, your role is full-time and on-site. You will utilize specialized equipment to monitor brain function, nerve conduction, and muscle activity in real-time during neurosurgeries. Your contribution as an Intraoperative Neuromonitorist is vital in helping surgeons make informed decisions and prevent unintended neurological damage. For this role, a bachelor's degree in neurophysiology, biomedical engineering, neuroscience, or a related field is typically preferred. Having coursework in neuroanatomy, electrophysiology, and clinical neurophysiology can be advantageous. Basic knowledge of neurophysiology, familiarity with monitoring equipment like EEG, EMG, and EP, as well as proficiency in data analysis software and medical monitoring systems are essential technical skills. While not always mandatory, certifications like CNIM (Certified Neurophysiological Intraoperative Monitoring) can be beneficial. Essential soft skills include attention to detail, effective communication to convey findings and collaborate with medical teams, and problem-solving abilities to address issues during monitoring. Hands-on experience through internships, clinical rotations, or academic projects related to neurophysiology can add value. Attributes such as a commitment to continuous learning, staying updated with advancements in neurophysiological monitoring and related technologies, and upholding ethical standards including patient confidentiality and professional conduct are important. The interview for this position is scheduled for 21st August 2024. To apply, please send your resume to maheshwari@acuteneuromonitoring.com. Further instructions regarding document submission will be provided via email.,

You are invited to join our Sales Team as a Sales Engineer. In this role, you will collaborate closely with the sales team and customers to comprehend requirements, showcase products and solutions, and finalize deals. Your primary objective will be to enhance sales growth by offering tailored product and technical support to our valued customers. Your responsibilities will include identifying and evaluating leads in collaboration with the sales team, delivering technical support and expertise to customers, demonstrating product features through presentations, suggesting products and solutions according to customer needs, cultivating and nurturing strong customer relationships, staying abreast of competitive products and industry trends, and achieving or surpassing sales targets. To excel in this role, you should possess a relevant degree or Diploma in Medical Electronics and Biomedical Engineering, along with robust technical and communication skills. Your ability to forge solid relationships with customers and teams will be crucial. Proficiency in Microsoft Office, particularly in MS Word and MS Excel, is essential. Preference will be given to candidates with training or internship experience in Hospital Medical equipment or Biomedical field. This is a Full-time, Permanent opportunity suitable for Freshers. The work schedule includes Day shift, Fixed shift, and Morning shift. The work location is in person.,

We are looking for a highly skilled and experienced Biomedical Engineer to join our team at Raigad Hospital and Research Centre. Roles and Responsibility Design, develop, and test biomedical devices and systems. Collaborate with cross-functional teams to identify and prioritize project requirements. Develop and implement testing protocols for biomedical devices. Analyze data and troubleshoot issues with biomedical devices. Ensure compliance with regulatory standards and guidelines. Participate in the development of technical documentation and reports. Job Requirements Bachelor's degree in Biomedical Engineering or related field. Proven experience in designing and developing biomedical devices and systems. Strong understanding of medical devices and regulations. Excellent problem-solving and analytical skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills.

Optra Scan Pvt Ltd is a renowned provider of digital pathology solutions, transforming the landscape of pathology practices worldwide by streamlining the management and interpretation of diagnostic information. With our innovative technology, we empower pathologists to enhance efficiency, precision, and patient care through the integration of digitalization and artificial intelligence. As a Technical Writer - Regulatory at OptraSCAN, you will play a pivotal role in creating, organizing, and updating regulatory documentation essential for product approvals, certifications, and market entry across global jurisdictions. This position demands a blend of strategic regulatory planning and meticulous technical writing focused on ensuring adherence to international standards like ISO 13485, FDA 21 CFR Part 820, EU MDR, and other relevant regulations. Your responsibilities will include preparing and managing various regulatory documents such as Technical Files, Design Dossiers, Clinical Evaluation Reports (CERs), Risk Management Files, Declarations of Conformity, and FDA submissions. Collaboration with cross-functional teams comprising R&D, QA, Clinical, and Marketing departments will be essential to gather inputs for the compilation of submission materials. In the realm of technical writing, you will be tasked with crafting, reviewing, and refining Standard Operating Procedures (SOPs), work instructions, user manuals, labeling, and Instructions for Use (IFUs) to ensure accuracy, clarity, and regulatory compliance. Your ability to translate intricate technical information into easily comprehensible documentation will be critical in this role. Staying abreast of regulatory updates such as EU MDR and FDA guidelines will be imperative to ensure that internal processes and documentation align with the latest standards. Compliance with key regulations like ISO 13485, ISO 14971, IEC 62304, IEC 60601, EU MDR 2017/745, and FDA 21 CFR Part 820 will be a focal point of your responsibilities. Moreover, you will provide support for internal audits and inspections by maintaining meticulous and readily accessible documentation. Assistance in Corrective and Preventive Actions (CAPA) documentation and post-market surveillance reporting will also be expected as part of your Quality System Support duties. To qualify for this role, you should hold a Bachelor's or Master's degree in Life Sciences, Biomedical Engineering, Pharmacy, or a related field, accompanied by at least 3-6 years of experience in regulatory writing or regulatory affairs within the medical device or healthcare product domain. Proficiency in global medical device regulatory frameworks, exceptional written English and technical writing skills, as well as strong organizational and project management capabilities are essential prerequisites. Preferred qualifications for this position include prior experience in preparing 510(k) submissions, CE Mark applications, or similar regulatory filings. Knowledge of digital pathology, imaging devices, or software as a medical device (SaMD) would be advantageous, along with a certification in Regulatory Affairs such as RAPS RAC. Join Optra Scan Pvt Ltd in revolutionizing the digital pathology landscape and leveraging your regulatory expertise to drive impactful advancements in healthcare technology.,

Aster Medcity is looking for Senior Executive - Insurance to join our dynamic team and embark on a rewarding career journey Lead and manage the day-to-day operations of the insurance department, including underwriting, policy issuance, premium collection, and claims administration. Develop and implement strategies to enhance operational efficiency, streamline processes, and optimize workflow in accordance with industry best practices and regulatory requirements. Monitor key performance indicators (KPIs), metrics, and operational targets to assess departmental performance, identify areas for improvement, and drive continuous process improvements. Oversee the underwriting process, including risk assessment, policy evaluation, and pricing decisions, to ensure adherence to underwriting guidelines, risk appetite, and profitability targets. Manage the claims adjudication process, including claim intake, investigation, evaluation, and settlement negotiations, to ensure timely and accurate resolution of claims in compliance with policy terms and conditions. Provide leadership, guidance, and support to insurance professionals and support staff, including training, mentoring, performance coaching, and career development opportunities. Foster strong relationships with insurance carriers, brokers, agents, and external stakeholders to facilitate business development, collaboration, and partnership opportunities. Collaborate with cross-functional teams, including finance, legal, compliance, and IT departments, to address operational challenges, implement system enhancements, and ensure regulatory compliance.

As a Biomedical Engineering Technician, you will play a crucial role in the maintenance, troubleshooting, and repair of medical equipment within a healthcare facility This position involves working closely with medical staff, vendors, and other technicians to ensure the proper functioning of a wide range of biomedical devices The ideal candidate should have a strong technical background in biomedical engineering, excellent problem-solving skills, and a commitment to maintaining the highest standards of patient care Responsibilities: Equipment Maintenance:Perform routine preventive maintenance on a variety of biomedical equipment, ensuring compliance with regulatory standards Conduct inspections to identify and address potential issues before they impact patient care Repair and Troubleshooting:Diagnose and repair malfunctions in biomedical equipment, including diagnostic imaging devices, patient monitors, infusion pumps, and laboratory instruments Collaborate with vendors and manufacturers to resolve complex technical issues Calibration:Calibrate and adjust equipment to ensure accuracy and consistency in measurements and performance Maintain calibration records and documentation Documentation:Maintain comprehensive records of equipment maintenance, repairs, and service history Ensure all documentation complies with regulatory requirements and quality standards Training and Support:Provide training and support to medical staff on the proper use and care of biomedical equipment Assist in developing training materials and conducting educational sessions Equipment Upgrades:Collaborate with vendors and internal stakeholders to implement upgrades or modifications to existing equipment Evaluate the feasibility and impact of equipment enhancements Inventory Management:Manage and track inventory of spare parts, tools, and supplies related to biomedical equipment Reorder supplies as needed to ensure adequate stock levels Compliance and Regulations:Stay informed about industry regulations, standards, and best practices related to biomedical equipment Ensure all equipment and activities comply with relevant regulatory requirements

As a Biomedical Engineer working on hospital-based clinical trials for CanScan, you will play a crucial role in ensuring the successful completion of trials at our sites in Mangalore and Rishikesh. You will be responsible for overseeing the operation, maintenance, and troubleshooting of medical equipment, as well as managing inventory and logistics of consumables. Your dedication to regulatory compliance, seamless trial execution, and high-quality reporting will be essential for the success of the research. Your key responsibilities will include handling medical equipment setup, calibration, and maintenance in hospital settings, monitoring CanScan sensor performance during trials, ensuring protocol compliance and data accuracy, drafting detailed trial reports, and coordinating with stakeholders such as principal investigators and hospital staff. Your role will also involve maintaining documentation, managing equipment logistics, and supporting day-to-day trial operations. To excel in this position, you should hold a degree in Biomedical Engineering or a related field and have hands-on experience with medical devices like ventilators, CPAP, and BiPAP. Prior involvement in clinical trials or hospital-based research, along with strong knowledge of clinical trial protocols, statistical analysis, and reporting, will be beneficial. Effective communication and organizational skills are essential for collaborating with medical and research teams, and familiarity with regulatory frameworks such as GCP standards, ICMR, and FDA regulations will be highly advantageous. If you are ready to take on this challenging yet rewarding role, where you will contribute to groundbreaking research and work closely with a dedicated team of professionals, we invite you to apply and be a part of our innovative journey in healthcare.,

You will be joining an early-stage MedTech startup with a mission to design and develop accurate, affordable, and accessible medical equipment for both the Indian and global markets. Your work will focus on biomedical innovation, user-centric design, and social impact, aiming to reimagine healthcare delivery, especially in under-served markets. As a core team member, you will have a pivotal role in shaping the technical foundation, culture, and direction of the company. This will include leading the end-to-end design and development of innovative medical devices, translating clinical needs into technical specifications, overseeing design validation and regulatory compliance, collaborating with external partners, managing and mentoring junior engineers, participating in grant proposals and product strategy discussions, supporting regulatory submissions, and staying updated on emerging biomedical technologies and trends. To qualify for this role, you should have an M.Tech/M.E. in Biomedical Engineering or a related field, with at least 5-7 years of hands-on experience in designing and developing medical devices, preferably Class I or II. You should have a strong foundation in biomedical instrumentation, electronics, sensors, or mechanical aspects of device design, as well as experience with CAD tools, circuit design, embedded systems, or signal processing. Knowledge of product lifecycle management, prototyping, testing, and Design for Manufacturing is also required, along with familiarity with clinical workflows, anatomy/physiology, user-centric healthcare design, regulatory frameworks, standards, and risk management. Additionally, preferred attributes for this role include a startup mindset, strong problem-solving abilities, the capacity to work independently in an unstructured environment, a passion for improving healthcare access and quality through innovation, and excellent communication and collaboration skills. In return, you will have the opportunity for a founding team role with equity/ESOP potential, the chance to shape next-generation MedTech solutions with real-world impact, exposure to leading hospitals, research institutes, and design collaborators, and a culture of innovation, purpose, and long-term vision.,

Aster Medcity is looking for Junior Biomedical Engineer.Biomedical Engineering.Aster MIMS Kannur to join our dynamic team and embark on a rewarding career journeyDesign and develop medical devices, equipment, and software that meet clinical and regulatory requirements.Collaborate with cross-functional teams, including physicians, nurses, technicians, and other engineers, to define product requirements and specifications.Conduct feasibility studies, risk assessments, and design verification and validation activities to ensure that products meet regulatory and clinical requirements.Develop and maintain documentation, including design specifications, test plans, and reports, to ensure that products are developed in compliance with regulatory standards.Design and develop software algorithms and applications that support medical devices and equipment.Develop and maintain quality control processes and procedures to ensure that products are manufactured and maintained to a high standard.Participate in the development of clinical trials and studies to evaluate the safety and effectiveness of medical devices and equipment.Strong communication and collaboration skills, with the ability to work effectively in cross-functional teams.

Role & responsibilities Travel to multiple government hospitals to address complaints reported by end-users. Diagnose issues and take necessary actions to resolve complaints promptly. Provide clear updates,regarding the status of complaints and actions taken. Complete preventive maintenance Services(PMS) as per the scheduled plan. Conduct user training sessions for end users to ensure they can operate equipment efficiently. Ensure all tasks are completed with the goal of maintaining customer satisfaction and delight. Manage time effectively to attend to all complaints within the allocated timeframe. Preferred candidate profile Minimum 2 to 4 years of experience required. If you are interested, Please share CV's to raisy.p@cyrix.in

Job Description: About Achievers Spot Medical Coding is the Fastest-growing Profession in the Healthcare Industry Today. It is a Niche Specialization and the Demand for Trained and Certified Medical Coders is Increasing Exponentially and Bound to Increase in Upcoming Years, Especially in India. you have At Least a Diploma/degree in Any Field. this Role is Open to Fresh Graduates with Excellent English Communication Skills. you Pay Strong Attention to Details and are Capable of Delivering Top-quality Work you are Goal-oriented and Thrive in Fast-paced Environments maintains a Working Knowledge of Cpt-4, Icd-10-cm, and Icd-10-pcs Coding Principles, Governmental Regulations, Uhdds (uniform Hospital Discharge Data Set) Guidelines, Aha Coding Clinic Updates, and Third-party Requirements Regarding Coding and Documentation Guidelines Contact Us: HR SHANMUGAPRIYA 8072891550

You specialize in providing acute neuromonitoring services, focusing on continuous monitoring of patients" neurological functions during critical periods like neurosurgeries and acute neurological conditions. Your main goal is to detect any changes in neurological status promptly for timely interventions and management. As an Intraoperative Neuromonitorist based in Bengaluru, you will work full-time on-site. Your responsibilities include utilizing specialized equipment to monitor brain function, nerve conduction, and muscle activity in real-time during neurosurgeries. Intraoperative Neuromonitorists are essential in helping surgeons make informed decisions and prevent inadvertent neurological damage. For educational background, a bachelor's degree in neurophysiology, biomedical engineering, neuroscience, or a related field is typically preferred. Courses in neuroanatomy, electrophysiology, and clinical neurophysiology are advantageous. In terms of technical skills, you should have a basic understanding of neurophysiology, including brain and nervous system functions and common neurophysiological monitoring techniques. Familiarity with equipment like electroencephalography (EEG), electromyography (EMG), and evoked potentials (EP) is beneficial. Proficiency in using data analysis software and medical monitoring systems is also required. Certifications like the CNIM (Certified Neurophysiological Intraoperative Monitoring) can be advantageous but not always mandatory. Soft skills such as attention to detail, effective communication, and problem-solving abilities are crucial. You should be precise in monitoring and interpreting neurophysiological data, collaborate well with medical teams, and address issues during monitoring. Hands-on experience gained through internships, clinical rotations, or academic projects related to neurophysiology is valuable. A commitment to continuous learning and staying updated with advancements in neurophysiological monitoring and related technologies is essential. Adherence to ethical standards regarding patient confidentiality and professional conduct is a must. Please note that the interview is scheduled for 21st August 2024. To apply, kindly send your resume to maheshwari@acuteneuromonitoring.com. Further details for submitting required documents will be communicated via email.,

As a Service Engineer specializing in PCB Repairs, you will be responsible for repairing and replacing faulty PCB components in medical devices using precision tools. Your primary duties will include installing, maintaining, and repairing medical devices, ensuring their proper functionality, diagnosing and fixing technical issues, and identifying faults in PCB components and circuits. You will be expected to take prompt corrective actions for breakdown calls within the specified time frame, respond promptly to service requests, and resolve technical issues in medical devices including Criticalcare and life-support systems. Additionally, you will be required to detect and resolve faults in PCBs, SMD components, and electrical circuits, and perform repairs on key components such as PCBs, SMD components, ICs, and resistors. To qualify for this role, you should hold a Diploma or Bachelor's degree in Electronics, Electrical, Biomedical Engineering, or a related field. You should have 2-3 years of experience in PCB repair within the medical device industry and possess proficiency in diagnosing and repairing PCBs, including SMD and through-hole components. This is a full-time position with a day shift schedule located in Delhi NCR. You will also be responsible for providing on-site and remote technical support to customers and collaborating with the team to troubleshoot complex issues and find innovative solutions to enhance device performance and reliability.,

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

Urgent Requirement of Biomedical Engineer@ Amrita Hospital Faridabad Exp - 2 to 5yr Qualification - BTech (Biomedical) Salary - As per industry norms Interested Candidates Can Contact - Rahul Chauhan - 9911892435 Email ID - rahul.chauhan@fbd.amrita.edu

We are seeking an experienced and skilled CSSD Product Engineer to join our team. The successful candidate will be responsible for developing, and implementing sterile packaging and processing solutions for medical devices and equipment. The CSSD Product Engineer will play a critical role in ensuring the safety, quality, and efficacy of our products. Key Responsibilities: 1. Product Testing and Validation : Conduct testing and validation of sterile packaging and processing solutions to ensure they meet design specifications, regulatory requirements, and industry standards. 2. Process Improvement : Continuously evaluate and improve sterile packaging and processing solutions, implementing changes as needed to ensure optimal safety, quality, and efficacy. 3. Regulatory Compliance : Ensure compliance with regulatory requirements, such as FDA, ISO, and CE marking, for sterile packaging and processing solutions. 4. Collaboration and Communication*: Collaborate with cross-functional teams, including R&D, manufacturing, and quality, to ensure effective communication and coordination of product development and launch activities. 5. Technical Support : Provide technical support and guidance to internal stakeholders, including manufacturing, quality, and customer service, on sterile packaging and processing solutions. 6. Industry Trends and Standards : Stay up-to-date on industry trends, standards, and regulatory requirements, applying this knowledge to inform design and development activities. 7. Documentation and Record-Keeping : Maintain accurate and complete documentation and records of design and development activities, testing and validation results, and regulatory compliance. Requirements: - Bachelor's degree or Diploma in Engineering (e.g., Mechanical, Biomedical, Packaging), or related field. - Minimum 1-5 years of experience in product or a related field, preferably in the medical device industry. - Strong knowledge of sterile packaging and processing solutions, development, testing, and validation. - Experience with regulatory requirements, such as FDA, ISO, and CE marking. - Excellent problem-solving, communication, and collaboration skills. - Ability to work in a fast-paced environment and prioritize multiple projects simultaneously.,