156 Biomedical Engineering Jobs - Page 2

Post : Biomedical Engineer Organization : Park Hospital, Sector-47, Gurgaon, Haryana, Qualification : Degree/Diploma in Biomedical Experience : Experienced (2-10 Yrs) Required Position : 03 (Senior & Junior) Location : Gurgaon Industry : Hospital/Healthcare Remuneration: Best in hospital industry Job Responsibilities: Provides technical support Responds to user inquiries Maintains biomedical machine and equipment Generates reports on machine performance Trains machine operators on proper usage of equipment liaising with medical and scientific staff and patients to understand their needs designing, developing and testing products, equipment and devices that will address medical problems cost efficiently designing, testing and implementing new medical procedures, such as computer-aided surgery and tissue engineering managing clinical trials of new devices and equipment working with manufacturers of devices and their marketing teams investigating ways to market new products maintaining equipment and training staff to use it safely responding to queries and resolving problems with devices writing reports and documentation Installing and modifying medical equipment and instruments within hospitals, health centres, and extended care facilities Ensuring the safety of medical equipment used for diagnosis, treatment, and monitoring of patients Design and develop devices to assist with a physical disability, such as prostheses Design and evaluate the efficacy of medical devices, such as pacemakers, dialysis machines, and patient monitors Study medical systems and products to prepare and present reports to research groups, hospital boards, or professional associations Develop and improve medical technology, such as surgical lasers and artificial hips and knees Supervision of biomedical technicians and technologists Interested candidate can attend walking interview at 11:00am or send their resume at gurgaon@parkhospital.in Regards HR Team Park Hospital, Sector-47, Gurgaon

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.,

Responsibilities: * Design, develop & maintain medical equipment * Collaborate with healthcare teams on device integration * Ensure compliance with regulatory standards * Conduct regular calibrations & preventative maintenance Provident fund

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

* Study historic inventory records and prepare forecasts of the requirement. * Responsible for Equipment installation, adjust, maintain, repair, or provide technical support for biomedical equipment. * Responsible for maintenance, calibration and day to day troubleshooting of medical equipments. * Should co-ordinate with company engineers in minimizing the down time of the equipment for calibration, maintenance and troubleshooting. * New equipment has to be added to the finance data (FA Register) and asset No. needs to be fixed on the equipment. * Sticker is placed on the equipment for the next PM and Calibration due date. * Consult organizational purchase, procurement team and Center Manager to be aware of rate contracts of AMC/CMC by negotiating with vendors . * After an indent is raised by the Incharge Nurse BME needs to discuss with concerned users and final discussion with Center Manager and Procurement Head and after which their approval can commence procurement process. * Carry-out negotiations with multiple vendors, evaluate and finalize the reliable and cost-effective vendors for procurement of materials. * After the Final Approval the PO will be raised either by BME/ Procurement team. * Evaluate the safety, efficiency, and effectiveness of biomedical equipment and instruments. * Train Nurses and OT Technicians and other personnel on the proper use of equipment. * Ensure the material purchased is of the agreed quality & meets the minimum standards set by the quality department. * Interface with all the departments in a periodic manner to ascertain the needs of various materials in each department. * Maintain the equipment details and track the prompt usage of the equipments. * Support Center Medical & Quality head in tracking the right equipment for the particular surgeries. * Maintain sources for all emergency supply items from other vendors and other branches of NOVA. * Ensure safe transport of the materials to the center. * Ensure all the SOPs are followed in the transportation and storage of the materials as per PO . *

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.,

MEDI ANALYTIKA IS RECOGNIZED AS THE LARGEST INSTRUMENTATION COMPANY IN INDIA HAVING TIE UPS WITH 50+ WORLD LEADING INSTRUMENTATION COMPANIES FROM USA - CANADA - UK - EUROPE - JAPAN - REPUBLIC OF KOREA - ISRAEL. Our existing clients include all major universities, research institutions, hospitals, pharmaceutical / CROs, food processing companies, chemical industries and other industries. Role & responsibilities : As a service engineer, you will have to visit our clients spread all over India to install and also provide after sales service support.

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.,

Role & responsibilities Install and maintain ophthalmic equipment (e.g. phaco machines, OCT, slit lamps, lasers). Perform preventive maintenance and timely repairs. Ensure equipment calibration and safety compliance. Maintain service logs and support audits. Assist in procurement, inventory, and vendor coordination. Preferred candidate profile Bachelors Degree in Biomedical Engineering or related field 3+ years of experience (preferably in eye care or hospital setup) Interested candidates may contact on 8610205221 with below mentioned details

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.,

Location : Surat Industry: Pharma Industry Contact:** +91 90816 99800 Biomedical Job Opening Role: Biomedical Technician / Executive Salary: 20,000 – 25,000 per month Timings: 9:00 AM – 6:00 PM Location: Pal, Surat . Required Candidate profile Medical Representative Job Opening Role: Medical Representative (MR) Salary: 20,000 – 25,000 per month Timings: 9:00 AM – 6:00 PM Location: Surat 91 90816 99800

Dear Candidate, Job opening at Paras Health Care Ltd Position - Senior Executive - Biomedical Experience Required - 0 To 4 Years Salary Range - As per Market Standard Experience & Qualification Diploma/ Degree in relevant Specialization (ITI, B.Sc - Instrumentation, B.E, B.Tech - Electronics, Biomedical, Instrumentation) Fresher or with an experience of 4 years. Specific Responsibilities The responsibilities are as follows: To coordinate and evaluate the work performed by service contractors including maintenance, calibration, installation and verification of service documentation. To monitor monthly schedule of plan preventive maintenance & calibration. To provide training for related facility staff on maintenance and utilization of equipment's. Renewal of AMC / CMCs of medical equipment's. Indent approval. Monitor complaint register / History card. To supervise staff in repair & maintenance. To negotiate with vendors regarding repairs. Ensures 90 % uptime for all medical equipment's Downtime should not more than 72 hours except major breakdown. Provides critical inputs which help decision making for procurement of various medical equipment's. Effective evaluation of new equipment specifications technological advancement of the hospital. Planning, distribution and costing, negotiating and all the other activities associated with setting up/starting a new facility. Perform any other duty that may be assigned from time to time. Skills: biomedical engineering,opto-mechanical engineering,medical equipment,amc,cmc,instrumentation,maintenance,

Role & responsibilities Install, test, and maintain biomedical equipment as per industry standards Conduct regular preventive maintenance and inspections Ensure timely calibration and servicing of medical devices Troubleshoot equipment issues and coordinate with vendors for repairs Maintain comprehensive records of equipment history and service reports Train hospital staff on proper use and care of medical equipment Stay updated with technological advancements in biomedical engineering Preferred candidate profile Bachelor's degree/Diploma in Biomedical Engineering or related field Minimum 5 to 10 years of relevant experience preferred (freshers with strong technical skills may also apply) Knowledge of hospital-grade diagnostic and therapeutic equipment Familiarity with NABH standards will be an added advantage Strong problem-solving, communication, and technical skills

No. of Vacancies : 1 Location : Raiganj Department : Maintenance Qualification : B.Tech/B.E. in Biomedical Engineering Experience : 2 - 5 years experience in any hospital as a biomedical engineer providing evaluation, replacement, service and support to the medical equipment during their breakdown, obtaining maintaining regulatory norms from AERB, PNDT etc, maintenance of asset register across all asset, conducting preventive maintenance of all equipment maintenance of stock of spares.

DY Patil University is a trailblazer in Education, Sports, and Healthcare, dedicated to excellence and innovation. As we continue to grow, we're seeking a passionate employees to contribute to the visual identity of our esteemed institution.