22 TONBO IMAGING JOBS

Clinical Application Specialist (MR/CT/DSA)Location: Hyderabad, IndiaWho we are?Shanghai United Imaging Healthcare Co., Ltd. is dedicated to providing, developing and producing high-performance advanced medical imaging, radiotherapy equipment, life science instruments and offers intelligent digital solutions to customers worldwide. UIH is committed to creating more value for our customers and constantly improving the global accessibility of high-end medical equipment and services through in-depth cooperation with hospitals, universities, research institutions, and industry partners.Join our innovative team with the mission of developing and supplying advanced technologies and improving patient care worldwide. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.Company Page: http://www.united-imaging.com/en/home/ Job SummaryThe Clinical Application Specialist will be responsible for driving and executing the clinical application and operation training for health systems, hospitals, diagnostic imaging, and oncology centers. The successful candidate will take the responsibility of increasing customer satisfaction and productivity by providing outstanding, high-quality application training and support to customer for high-end medical imaging systems.The job responsibilities include:Make training plans and timely complete the clinical application training of related products (CT/MR/DSA) in the area under responsibility;Discover and solve customer’s clinical problems in time, improve customer satisfaction, and establish long-term customer relationships;Collect customer feedback and excellent clinical images/cases, and summarize them to support product sales and new product research;Assist in establishing regional expert resources, maintain expert relations, and support customers to carry out clinical scientific research;Responsible for the establishment and maintenance of reference hospitals in the responsible region, and responsible for the reception of reference hospitals’ visiting;Assist the sales and MKT team to achieve the company's sales targets and business growth by providing pre-sales/after-sales product/application demonstration support, as well as assisting in organizing various promotions and exhibitions.Other tasks assigned by supervisors.Your Qualification and Experiences Requirements:Bachelor's degree or above, major in medical imaging diagnosis, medical imaging technology, or related field;5+ years’ experience as a radiographer or radiologist in the healthcare industry, or 3+ years of experience as an application specialist in one specific modality field, familiar with CT/MR products, technology, and operation knowledge;Excellent communication, presentation, and persuasion skills; good customer service awareness;Excellent teamwork ability, enjoy working with people, and committed to providing excellent customer satisfaction;Strong sense of responsibility, strong ability to work under pressure, adaptable to frequent business travel;Experience in other manufacturers (e.g. GE, Philips, Siemens) is a plus.Key Competences:On-site training Development history and cutting-edge technology of the imaging industry;Basic knowledge of clinical medicine (diseases of various systems and their pathophysiological changes);Basic knowledge of clinical imaging diagnosis;Imaging principle and clinical application of imaging technology (application level);Image-related image post-processing software (application level);Customer relationship maintenance.

We are seeking a skilled Electro-Mechanical Technician to join our team. The ideal candidate will be responsible for installing, troubleshooting, repairing, and maintaining electro-mechanical systems and equipment. This role involves working with electrical and mechanical components, reading technical diagrams, and ensuring equipment operates efficiently and safely.Key ResponsibilitiesDiagnose and resolve electrical and mechanical issues using testing equipment and tools.Conduct diagnosis through troubleshooting to find out the cause of failure.Undertake repairs related to electronics & mechanical components as per the writteninstructions and procedures.Perform all work in accordance with quality standards and established safety procedures.Maintain a clean and safe work area.Ensure serviceability and calibration of measuring instruments and gauges.Perform system level testing of electro optics products.Ensure proper documentation and report generation.Maintain stock of finished products, spares, assembly/testing tools to meet customer requirements. Flexible to take service calls & visit customer locations for field support.Quality Control for mechanical / electronic components & processes.Working knowledge on testing of PCBs / electrical systems is desirable.IQC of mechanical parts, PCBs, Cables and electronic accessories (batteries,chargers, adapters) and inspection report generation.Record and report system performance, repairs, and maintenance activities.Maintain inventory of tools, spare parts, and equipment.Qualifications and SkillsEducation: Diploma or degree in Electronics / Mechanical Technology/ Mechatronics, or related field.Experience: 2+ years in electro-mechanical maintenance or related roles.Technical Skills:Strong knowledge of electrical and mechanical systems.Proficiency with diagnostic tools and software.Soft Skills:Strong problem-solving and analytical skills.Good communication and teamwork abilities.Attention to detail and ability to work under pressure.

We are seeking a skilled Electro-Mechanical Technician to join our team. The ideal candidate will be responsible for installing, troubleshooting, repairing, and maintaining electro-mechanical systems and equipment. This role involves working with electrical and mechanical components, reading technical diagrams, and ensuring equipment operates efficiently and safely.Key ResponsibilitiesDiagnose and resolve electrical and mechanical issues using testing equipment and tools.Conduct diagnosis through troubleshooting to find out the cause of failure.Undertake repairs related to electronics & mechanical components as per the writteninstructions and procedures.Perform all work in accordance with quality standards and established safety procedures.Maintain a clean and safe work area.Ensure serviceability and calibration of measuring instruments and gauges.Perform system level testing of electro optics products.Ensure proper documentation and report generation.Maintain stock of finished products, spares, assembly/testing tools to meet customer requirements. Flexible to take service calls & visit customer locations for field support.Quality Control for mechanical / electronic components & processes.Working knowledge on testing of PCBs / electrical systems is desirable.IQC of mechanical parts, PCBs, Cables and electronic accessories (batteries,chargers, adapters) and inspection report generation.Record and report system performance, repairs, and maintenance activities.Maintain inventory of tools, spare parts, and equipment.Qualifications and SkillsEducation: Diploma or degree in Electronics / Mechanical Technology/ Mechatronics, or related field.Experience: 2+ years in electro-mechanical maintenance or related roles.Technical Skills:Strong knowledge of electrical and mechanical systems.Proficiency with diagnostic tools and software.Soft Skills:Strong problem-solving and analytical skills.Good communication and teamwork abilities.Attention to detail and ability to work under pressure.

We are seeking a skilled and customer-focused Customer Support Engineer to joinour Bangalore team. The ideal candidate will be responsible for providing technicalassistance, troubleshooting customer issues, and ensuring a seamless customerexperience. You will act as a bridge between customers and the technical team,resolving inquiries and delivering high-quality solutions in a timely manner.Key Responsibilities1. Customer Assistance:o Serve as the first point of contact for customer support inquiries viaemail, phone, or chat.o Provide technical guidance and resolve issues related to thecompany’s products or services.2. Troubleshooting and Problem Resolution:o Diagnose and troubleshoot hardware, software related problems.o Collaborate with internal teams to escalate and resolve complexissues.o Maintain detailed documentation of issues, resolutions, and feedback.3. Technical Expertise:o Provide in-depth knowledge of the company’s products, systems, andservices to customers.o Assist customers with usage of the products.4. Feedback and Improvement:o Gather and communicate customer feedback to internal teams forproduct improvements.5. Service-Level Adherence:o Ensure timely resolution of customer issues within agreed service levelagreements (SLAs).o Monitor and prioritize support tickets to meet customer expectations.Qualifications and Skills? Education:o Bachelor’s degree in engineering, Electrical,Electronics, Mechanical ora related field (or equivalent experience).? Experience:o 1-3 years of experience in technical support, customer service, or arelated role.o Prior experience in troubleshooting.? Technical Skills:o Familiarity with ticketing systems (e.g., Zoho Desk, Zendesk,Freshdesk) and CRM tools.? Soft Skills:o Excellent verbal and written communication skills in both English andHindi.o Strong problem-solving abilities with attention to detail.o Customer-oriented mindset with the ability to handle challengingsituations professionally.Key Competencies? Analytical Thinking? Empathy and Patience? Time Management? Team Collaboration? Adaptability to Technology

Who we are?Shanghai United Imaging Healthcare Co., Ltd. is dedicated to providing, developing and producing high-performance advanced medical imaging, radiotherapy equipment, life science instruments and offers intelligent digital solutions to customers worldwide. UIH is committed to creating more value for our customers and constantly improving the global accessibility of high-end medical equipment and services through in-depth cooperation with hospitals, universities, research institutions, and industry partners.Join our innovative team with the mission of developing and supplying advanced technologies and improving patient care worldwide. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.Company Page: https://www.united-imaging.com/enJob SummaryThe Customer Service Engineer will be responsible for working with UIH India local customer service team to provide after-sales service for health systems, hospitals, diagnostic imaging, and oncology centers. The successful candidate will maintain and install equipment in a professional and workmanlike manner in accordance with the company standards and directives and customer requirements.The job responsibilities include:1) Support for installation of UIH diagnostic imaging equipment within a designated product range at the customer site;2) Work closely with Customer Care Center (regional and headquarter level) to carry out troubleshooting, maintenance, and updates of designated product modalities under supervision;3) Attend service training courses and work toward completion of UIH Professional Certificate to build competence in providing technical assistance and support to our customers;4) Escalate at appropriate situations when customer satisfaction is compromised and ensure contractual obligations are met.5) Other tasks assigned by supervisors.Your Qualification and Experiences Requirements:1) Degree or Higher Diploma in Electrical/ Electronic Engineering or Science related major;2) Familiar with the principle and structure of diagnostic imaging equipment (CT/ MR/PET, etc.);3) Good IT, Microsoft Office and Networking Infrastructure skills;4) Have the ability to find and troubleshoot faults in the field;5) Strong communication and coordination skills, good customer-oriented service manner, excellent team cooperation spirit;6) A flexible approach to work, travel and unsociable hours;Base Location? Hyderabad/Pune/DelhiKey Competences:1) System installation2) System configuration and debugging3) Trouble shooting4) Replacement of spare parts

Varex Imaging is hiring a Senior System Software Engineer in the fast-growing X-Ray Imaging Components division. This Software Engineer will bring real world experience to our team by developing software systems and libraries needed to manage data produced by flat panel x-ray detectors.We are looking for candidates that will thrive in a fast paced, self-directed environment that is able to hit the ground running in a critical division of our company. There will be opportunities to work both individually and as a team. This position involves writing C++ software that interacts with x-ray hardware components.Responsibilities :- Design, build, and unit test object-oriented software in a collaborative environment.- Will provide design, coding, testing, debugging, configuration, and software documenting.- Understands product development processes including Change Control & Design Control and SDLC- Strong software development, continuous integration, testing & troubleshooting skills.- Excellent oral and written communication skills- Ability to interface and communicate with internal and external customers across time zones.- Must be able to work with minimal supervision.Requirements :- At least a B.S. or M.S in Software Engineering or Computer Science- 8+ years relevant work experience- Fluency in C++ is a must.- Understanding and use of C++ templates is desired.- Experience with Microsoft and Linux operating systems and build tools is required.- Experienced with multi-threading is required.- Solid skills in Object-oriented Design and Analysis (OOA and OOD)- Experience with QT and UI development desired.- Ability to diagnose issues using log files.- Solid understanding of system level software (drivers, firmware, networking, wifi, and test applications) is highly desirable.- Understanding of Xilinx would be helpful.- Passion for developing efficient, testable, and well-documented code.- Prior work with imaging products or designing software products in an FDA or other regulated industry is highly desirable. (ref:hirist.tech)

Good knowledge in Electronics hardware.Knowledge of Cadence sch capture and PCB design tools.Good knowledge of Circuit Theory and Electronic DevicesShould have good hardware design and development knowledge (requirements definition, design, reviews, testing etc).Design knowledge in Analog and Digital CircuitsDigital design experience including micro-controllers, SPI, I2C, RS232,RS422, Ethernet etc.Analog design experience including active passive filters, amplifiers is helpful.Capable of conceptual design, parts selection, design simulation, detailed design, schematic capture and PCB design rules creation.Should be able to troubleshoot embedded boards/systems.Capable of writing supporting documentation to coordinate and establish layout practices and test procedures for the current design.Hands-on experience on using Lap tools like multimeter , Digital oscilloscope , spectrum analyzer , power supply etcDesign knowledge in analog and digital video interfacing will be a plus point.Design knowledge on EMI/ EMC will be a plus point.Good to have knowledge in c programmingGood written & verbal communication skills. Role and responsibility Responsible for the design and development of new products as well as the support and modification of existing products.Coordinate with layout teams to monitor correct guidelines are being followed.Manage prototype builds with contract manufacturers.Review Execute test protocols and document results.Support the boards and systems during environmental testing and entry into production.Be integral part of the Hardware Design Team as a driver of new ideas as well as provider of feedback for improvement of existing products.Continuous interaction with other departments (Software, Mechanical, etc) as part of daily board design practices and to support & maintain inter-departmental communications.Support board layout as well as board and system level bring-up, debug and verification.Involvement in customer support activities by site visits/giving demos /training /installation/solving customer's field issues is essential

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind. We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy.Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK; Leiden, Netherlands; Basel, Switzerland; Hyderabad, India and Shanghai, China. We are an affiliate of HonorHealth, one of the largest healthcare systems nationally, and Scottsdale Medical Imaging Limited (SMIL/RadPartners), the largest private radiology group in the United States. We are recognized as the world's largest and most preeminent iCRO in oncology.The Manager, Compliance and Regulatory Affairs is primarily responsible for assisting the Compliance and Regulatory Affairs Management in executing day-to-day tasks associated with managing, maintaining, and continually improving Imaging Endpoints' compliance to meet regulatory requirements. The Manager, Compliance and Regulatory Affairs is a compliance and solutions oriented individual; providing regulatory support to IE's iCRO and SMO.RESPONSIBILITIESRegulatory AffairsProvide regulatory assistance within the regulations of investigational products and quality standards, specifically: 21 CFR Part 312, 314, 50, 54,210, 211, 11, ICH E6(R2), Clinical Trials Imaging Endpoints Process Standards, GDPR, HIPAA, Risk Management, BIMO, and ISO 9001.Interface with Scientific Affairs, Operations, and Clinical departments on regulatory issues providing expertise and support as required.Develop and manage IE's regulatory intelligence program by assessing current regulatory trends in the industry and developing a process to identify, control, and maintain documents of external origin.Perform regulatory review and approval of scientific, clinical, QMS, and regulatory documents.Project specific (e.g., Imaging Manuals, Image Review Charters, Interim and Final Reports)Criteria assessmentsDeviations, CAPAs, and other investigations with regulatory impactRegulatory, clinical, and scientific standard operating procedures (SOPs)Business proposals, RFls, and other client facing documentsWork with SA and DM to provide regulatory guidance related to data or reporting used to support product submissions or communications to regulatory agencies.Interface with Compliance and Regulatory Affairs senior management to implement regulatory strategies and plans to facilitate continuous improvement of the QMS regarding regulatory affairs initiatives.Provide regulatory support for internal audits, sponsor audits, and regulatory inspections.Interface with vendors that provide Regulatory support and Compliance related services.Interface with Sponsors/CROs with respect to regulatory strategy and study requirements.Provide Regulatory training to IE personnel related to current industry practices and interpretation of FDA guidance, regulations, and standards.Assist the Chief Compliance and Regulatory Affairs Officer in establishing and reporting quality and regulatory metrics.Compliance and Document ManagementDevelop SOPs and controls related to regulatory requirements for GxP document management.Assist in establishing, implementing, and maintaining QA procedures and controls to develop an effective, efficient, and compliant IE QMS document change management program.Responsible for the quality of documentation created and approved to support GxP activities for IE and sponsor related projects.Perform other duties as assigned by Compliance and Regulatory Affairs senior management.Act in a supporting role to the QMS Specialist position.EDUCATION AND EXPERIENCEBachelor's degree in pharmaceutical sciences or other related scientific disciplines.Minimum six (6) years of experience in a regulated industry with at least four (4) years of experience in pharmaceuticals and/or medical device.QMS experience.Imaging Core Lab and/or Contract Research Organization experience preferred.Knowledge and understanding of 21CFR Part 211, 21CFR Part 312, IS 9001, and Good Clinical Practices (ICH E6 GCP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMPs) preferred.Proficiency in MS Office and internet applicationsPast experience with electronic document management systems in life sciences industry.SKILLSSuperior attention to detail, particularly in written documentationService oriented approach, flexible, and proactiveSelf-driven, ability to get the job done with little supervision, can-do positive attitudeAbility to excel in a team environmentAbility to work in strict compliance with all procedures, rules, and regulationsAbility to manage projects and deliverables with a high level of accuracy and completenessMaintain strict confidentiality of sensitive data, records, files, conversations, etc.Must be self-motivated and able to grasp new concepts quicklyExcellent hands-on computer skills with thorough knowledge of Microsoft Office to include Word, Excel and Power PointIMAGING ENDPOINTS' TEAM CHARACTERISTICSPassion to Connect Imaging to the Cure™ and pursue a meaningful career by improving the lives of cancer patients through imagingStrong desire to be part of a dynamic, global team working closely together and growing year after year in a rewarding environment to help humanity through imagingCommitment and caring for our fellow team members, their families, and the communities IE serves - see Caring Endpoints https://imagingendpoints.com/caring-endpoints/Integrity and high ethical standards; we always do the right thingHigh intellect and ingenuity; we enjoy solving problems, finding a better way, and the challenge of making a difference by improving livesStructured, organized, detail-oriented, and self-motivated; we approach each day with a detailed plan and excitement to accomplish the day's objectives while striving to improve ourselves and IE everydayAccountable; we do what we say and communicative effectively to meet deadlines; we enjoy advancing clinical trials, helping patients, and celebrating successHigh standard for excellence; we proof our own work, hold high standards for ourselves and our team, and always prioritize quality above all elsePHYSICAL REQUIREMENTS While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms and talk and hear. The employee is frequently required to sit. Specific vision abilities required by this job include close vision, color vision, ability to adjust focus.Travel: Estimated10-20% travel (domestic and international)

As a Senior Production Lead and Inventory Manager with over 10 years of experience in manufacturing industries, you will play a crucial role in overseeing production processes and managing inventory levels to ensure efficient operations. You will lead a team of production workers, coordinate production schedules, optimize inventory management strategies, and implement process improvements to enhance productivity and minimize costs. The ideal candidate will possess extensive experience in production leadership, inventory management, and a deep understanding of manufacturing processes.Key Responsibilities:Lead and supervise a team of production workers, providing guidance, training, and support to ensure optimal performance and productivity.Develop and implement production schedules, coordinating with various departments to meet production targets and customer demands effectively.Utilize advanced inventory management techniques to optimize inventory levels, minimize excess stock, and reduce carrying costs while ensuring materials availability for production needs.Implement inventory control measures to track inventory movements, prevent stockouts, and minimize shrinkage or loss.Collaborate with procurement and supply chain teams to source materials, negotiate supplier contracts, and ensure timely delivery of materials to support production schedules.Analyze production and inventory data to identify trends, forecast demand, and make data-driven decisions to improve inventory management processes.Lead continuous improvement initiatives to streamline production processes, reduce waste, and enhance operational efficiency.Ensure compliance with quality standards, safety regulations, and company policies in all production and inventory management activities.Develop and maintain relationships with key stakeholders, including suppliers, vendors, and internal departments, to support production and inventory objectives.Provide regular reports and updates to management on production and inventory performance, highlighting areas for improvement and recommending corrective actions as needed.Qualifications:Bachelor's degree in mechanical engineering is preferrableMinimum of 10 years of experience in production leadership and inventory management roles within manufacturing industries.Deep understanding of manufacturing processes, inventory management principles, and supply chain logistics.Proven track record of successfully leading teams, optimizing production processes, and implementing inventory management strategies.Strong analytical skills, with the ability to interpret data, identify trends, and make informed decisions to improve operations.Excellent communication, negotiation, and interpersonal skills, with the ability to collaborate effectively across departments and with external partners.Proficiency in inventory management software, ERP systems, and Microsoft Office Suite.Certifications in production management, inventory control, or supply chain management are a plus.

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the CureTM. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind. We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally that are passionate in their desire to assist us in our mission to customize each clinical trial’s imaging to optimize the opportunity to demonstrate efficacy.Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK; Leiden, Netherlands; Basel, Switzerland; Hyderabad, India and Shanghai, China. We are an affiliate of HonorHealth, one of the largest healthcare systems nationally, and Scottsdale Medical Imaging Limited (SMIL/RadPartners), the largest private radiology group in the United States. We are recognized as the world’s largest and most preeminent iCRO in oncology.Under the direction of Associate Director-Proposals, Sales Research Associate I is primarily responsible for the proposal and contract process within IE and shall coordinate with Business Development, Operations, Medical and Scientific Affairs, Finance, and Compliance and Regulatory Affairs to prepare, review, and negotiate proposals and change orders. This position will interact with potential clients, vendors, and other stakeholders and collaborate with internal staff across all departments.RESPONSIBILITIESPerform the responsibilities of the Sales Research Associate I as needed, plus the following additional responsibilities:Author proposals and perform QC of proposals authored by other team members.Coordinate with the proposal team to optimize proposal design by identifying and clarifying opportunities and needs described in RFPs and associated documentation. Integrate IE experience, key differentiators, and other industry best practices into proposals and presentations.Perform other duties as assigned by the supervisor.EDUCATION AND EXPERIENCE2 - 4 years of experience in the pharmaceutical or a regulated industry.1+ year of experience in medical imaging preferred.Prior experience in technical writing and/or proposal development preferred.Bachelor’s degree in English, Journalism, Marketing, Communications, Business, Computer Science / MIS, Science, Law, or related area.Knowledge and understanding of Good Clinical Practices.Prior experience in imaging clinical trials a must.Imaging Core Lab and/or Contract Research Organization experience preferred.SKILLSExcellent oral and written English language skillsPositive attitude, promoting a team spirit and professional environmentDetail oriented with strong organizational and analytical problem-solving skills.Understanding of best practices pertaining to software life cycle methodologies, ICH-GCP, 21 CFR Part 11Knowledge of software version control practices for maintaining reusable code and shared programming projects over extended periods of timeAbility to learn new systems and function in an evolving technical environmentAbility to successfully work independently and together with international teamsIMAGING ENDPOINTS’ TEAM CHARACTERISTICSPassion to Connect Imaging to the CureTM and pursue a meaningful career by improving the lives of cancer patients through imagingStrong desire to be part of a dynamic, global team working closely together and growing year after year in a rewarding environment to help humanity through imagingCommitment and caring for our fellow team members, their families, and the communities IE serves – see more information about Caring Endpoints at https://imagingendpoints.com/caring-endpoints/Integrity and high ethical standards; we always do the right thingHigh intellect and ingenuity; we enjoy solving problems, finding a better way, and the challenge of making a difference by improving livesStructured, organized, detail-oriented, and self-motivated; we approach each day with a detailed plan and excitement to accomplish the day’s objectives while striving to improve ourselves and IEAccountable; we do what we say and communicative effectively to meet deadlines; we enjoy advancing clinical trials, helping patients, and celebrating successHigh standard for excellence; we proof our own work, hold high standards for ourselves and our team, and always prioritize quality above all elseNote : Kindly send your update CV and the COVER LETTER* at nyennaboina@imagingendpoints.comIn your COVER LETTER, please answer the following: "How would you prioritize and summarize key research information for a pharmaceutical client in clinical trial imaging to prepare for an initial outreach call?"

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO). We are passionately focused on our vision to Connect Imaging to the Cure™. Everything we do is aligned with this singular purpose. We work every day excited to advance imaging science, technology, and services to bring curative technologies to humankind. We have supported many of the most impactful new drug approvals in oncology, and we are seeking the most talented individuals globally that are passionate in their desire to assist us in our mission to customize each clinical trial's imaging to optimize the opportunity to demonstrate efficacy.Imaging Endpoints is based in Scottsdale, Arizona, with offices in Cambridge, Massachusetts; London, UK; Leiden, Netherlands; Basel, Switzerland; Hyderabad, India and Shanghai, China. We are an affiliate of HonorHealth, one of the largest healthcare systems nationally, and Scottsdale Medical Imaging Limited (SMIL/RadPartners), the largest private radiology group in the United States. We are recognized as the world's largest and most preeminent iCRO in oncology.The Manager, Compliance and Regulatory Affairs is primarily responsible for assisting the Compliance and Regulatory Affairs Management in executing day-to-day tasks associated with managing, maintaining, and continually improving Imaging Endpoints' compliance to meet regulatory requirements. The Manager, Compliance and Regulatory Affairs is a compliance and solutions oriented individual; providing regulatory support to IE's iCRO and SMO.RESPONSIBILITIESRegulatory AffairsProvide regulatory assistance within the regulations of investigational products and quality standards, specifically: 21 CFR Part 312, 314, 50, 54,210, 211, 11, ICH E6(R2), Clinical Trials Imaging Endpoints Process Standards, GDPR, HIPAA, Risk Management, BIMO, and ISO 9001.Interface with Scientific Affairs, Operations, and Clinical departments on regulatory issues providing expertise and support as required.Develop and manage IE's regulatory intelligence program by assessing current regulatory trends in the industry and developing a process to identify, control, and maintain documents of external origin.Perform regulatory review and approval of scientific, clinical, QMS, and regulatory documents.Project specific (e.g., Imaging Manuals, Image Review Charters, Interim and Final Reports)Criteria assessmentsDeviations, CAPAs, and other investigations with regulatory impactRegulatory, clinical, and scientific standard operating procedures (SOPs)Business proposals, RFls, and other client facing documentsWork with SA and DM to provide regulatory guidance related to data or reporting used to support product submissions or communications to regulatory agencies.Interface with Compliance and Regulatory Affairs senior management to implement regulatory strategies and plans to facilitate continuous improvement of the QMS regarding regulatory affairs initiatives.Provide regulatory support for internal audits, sponsor audits, and regulatory inspections.Interface with vendors that provide Regulatory support and Compliance related services.Interface with Sponsors/CROs with respect to regulatory strategy and study requirements.Provide Regulatory training to IE personnel related to current industry practices and interpretation of FDA guidance, regulations, and standards.Assist the Chief Compliance and Regulatory Affairs Officer in establishing and reporting quality and regulatory metrics.Compliance and Document ManagementDevelop SOPs and controls related to regulatory requirements for GxP document management.Assist in establishing, implementing, and maintaining QA procedures and controls to develop an effective, efficient, and compliant IE QMS document change management program.Responsible for the quality of documentation created and approved to support GxP activities for IE and sponsor related projects.Perform other duties as assigned by Compliance and Regulatory Affairs senior management.Act in a supporting role to the QMS Specialist position.EDUCATION AND EXPERIENCEBachelor's degree in pharmaceutical sciences or other related scientific disciplines.Minimum six (6) years of experience in a regulated industry with at least four (4) years of experience in pharmaceuticals and/or medical device.QMS experience.Imaging Core Lab and/or Contract Research Organization experience preferred.Knowledge and understanding of 21CFR Part 211, 21CFR Part 312, IS 9001, and Good Clinical Practices (ICH E6 GCP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMPs) preferred.Proficiency in MS Office and internet applicationsPast experience with electronic document management systems in life sciences industry.SKILLSSuperior attention to detail, particularly in written documentationService oriented approach, flexible, and proactiveSelf-driven, ability to get the job done with little supervision, can-do positive attitudeAbility to excel in a team environmentAbility to work in strict compliance with all procedures, rules, and regulationsAbility to manage projects and deliverables with a high level of accuracy and completenessMaintain strict confidentiality of sensitive data, records, files, conversations, etc.Must be self-motivated and able to grasp new concepts quicklyExcellent hands-on computer skills with thorough knowledge of Microsoft Office to include Word, Excel and Power PointIMAGING ENDPOINTS' TEAM CHARACTERISTICSPassion to Connect Imaging to the Cure™ and pursue a meaningful career by improving the lives of cancer patients through imagingStrong desire to be part of a dynamic, global team working closely together and growing year after year in a rewarding environment to help humanity through imagingCommitment and caring for our fellow team members, their families, and the communities IE serves - see Caring Endpoints https://imagingendpoints.com/caring-endpoints/Integrity and high ethical standards; we always do the right thingHigh intellect and ingenuity; we enjoy solving problems, finding a better way, and the challenge of making a difference by improving livesStructured, organized, detail-oriented, and self-motivated; we approach each day with a detailed plan and excitement to accomplish the day's objectives while striving to improve ourselves and IE everydayAccountable; we do what we say and communicative effectively to meet deadlines; we enjoy advancing clinical trials, helping patients, and celebrating successHigh standard for excellence; we proof our own work, hold high standards for ourselves and our team, and always prioritize quality above all elsePHYSICAL REQUIREMENTS While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms and talk and hear. The employee is frequently required to sit. Specific vision abilities required by this job include close vision, color vision, ability to adjust focus.Travel: Estimated10-20% travel (domestic and international)

We are seeking a skilled CNC Milling Machine Operator to join our team. As a CNC MillingMachine Operator, you will be responsible for setting up, programming, and operating CNCmilling machines to produce precision components according to technical specifications. Theideal candidate will have experience with CNC milling machines and Master Cam Software,be detail-oriented, and possess a strong understanding of machining processes.Key Responsibilities:• Program CNC milling machines using G-code or other programming languages toexecute machining operations.• Proficiency in reading & interpret technical drawings, blueprints, and GD&T (GeometricDimensioning and Tolerancing) symbols and instructions to ensure accurateproduction.• Monitor machine operations and adjust as necessary to ensure proper cutting speeds,feeds, and tool paths.• Knowledge of machining processes, Measuring Instruments and materials & Attentionto detail and ability to maintain high quality and precision.• Strong mechanical aptitude and attention to detail.• Inspect machined parts for defects and ensure conformance to quality standards andspecifications.• Perform routine maintenance on CNC milling machines, such as cleaning, lubricating,and replacing worn components.• Troubleshoot and resolve basic machine issues to minimize downtime and maintainproductivity.• Collaborate with engineers, programmers, and other team members to optimizemachining processes and improve efficiency.• Adhere to safety protocols and always maintain a safe working environment.Requirements:• 2+ Years in CNC Milling Setting and Programming• Experience with Master Cam software.• Knowledge of CAD software preferable SolidWorks.• Knowledge of cutting tools, tool holders, and work holding devices.• Excellent problem-solving and troubleshooting skills.• Effective communication and teamwork abilities.• Willingness to work flexible hours as needed.

Responsibilities• Bring up the boards.• Debugging and testing of the boards.• Develop bench/test setups to determine and verify device performance.• Analyse and resolve all hardware test issues for the products.• Feedback to the design and production team regarding performance. Required Skill• This position requires a Degree/ Diploma in E&C, EEE with a minimum of 3 years of relevant experience.• Excellent hardware troubleshooting skills, knowledge about communication protocols like I2C, UART, RS422, Ethernet etc. • Knowledge about video interfaces like HDMI, CSI, Analog (CVBS) is a plus.• Understanding regarding schematic and board file is a plus.• Solid understanding of electronic circuits, mechanical systems, and/or software applications relevant to the testing process.• Strong analytical and problem-solving skills, with the ability to identify, troubleshoot, and resolve issues efficiently.• Detail-oriented mindset with excellent record-keeping and documentation skills.• Effective communication skills and the ability to work collaboratively within cross-functional teams.• Willingness to work in a hands-on, fast-paced environment while maintaining a high level of accuracy.

Good knowledge in Electronics hardware.Knowledge of Cadence sch capture and PCB design tools.Good knowledge of Circuit Theory and Electronic DevicesShould have good hardware design and development knowledge (requirements definition, design, reviews, testing etc).Design knowledge in Analog and Digital CircuitsDigital design experience including micro-controllers, SPI, I2C, RS232,RS422, Ethernet etc.Analog design experience including active passive filters, amplifiers is helpful.Capable of conceptual design, parts selection, design simulation, detailed design, schematic capture and PCB design rules creation.Should be able to troubleshoot embedded boards/systems.Capable of writing supporting documentation to coordinate and establish layout practices and test procedures for the current design.Hands-on experience on using Lap tools like multimeter , Digital oscilloscope , spectrum analyzer , power supply etcDesign knowledge in analog and digital video interfacing will be a plus point.Design knowledge on EMI/ EMC will be a plus point.Good to have knowledge in c programmingGood written & verbal communication skills. Role and responsibility Responsible for the design and development of new products as well as the support and modification of existing products.Coordinate with layout teams to monitor correct guidelines are being followed.Manage prototype builds with contract manufacturers.Review Execute test protocols and document results.Support the boards and systems during environmental testing and entry into production.Be integral part of the Hardware Design Team as a driver of new ideas as well as provider of feedback for improvement of existing products.Continuous interaction with other departments (Software, Mechanical, etc) as part of daily board design practices and to support & maintain inter-departmental communications.Support board layout as well as board and system level bring-up, debug and verification.Involvement in customer support activities by site visits/giving demos /training /installation/solving customer's field issues is essential

Good Knowledge of Allegro PCB Editor Ver 16.6 & 17.2 Tool and ORCAD Capture Tool- Complete understanding of PCB Layout process with knowledge of IPC standards- Design of Single Sided, Double sided and multilayer boards- Expertise in design of high-speed digital, Analog, Power circuits, RF & video signals, and design for EMI/EMC- PCB's Footprint (Decal) Creation as per IPC Standard- Knowledge about Signal integrity, EMC/EMI, Power integrity- Good sound understanding in BGA Routing with Blind ,Buried and micro via concept.- Should have knowledge of rigid flex PCB design- Good knowledge on Electronics Component- Sound familiarity with fabrication and assembly process- Should have a sound understanding of the DFM process for PCB- Basic circuit design knowledge

JOB DESCRIPTION – AR CALLER/MEDICAL BILLING Perform pre-call analysis and check the status by calling the payer or using IVR or web portal services Maintain adequate documentation on the client software to send the necessary documentation to insurance companies and maintain a clear audit trail for future reference Record after-call actions and perform post-call analysis for the claim follow-up Assess and resolve inquiries, requests, and complaints through calling to ensure that customer inquiries are resolved at the first point of contact Provide accurate product/ service information to the customer, research available documentation including authorization, nursing notes, medical documentation on client's systems, interpret explanation of benefits received, etc prior to making the call Perform analysis of accounts receivable data and understand the reasons for underpayment, days in A/R, top denial reasons, use appropriate codes to be used in documentation of the reasons for denials/underpayments JOB REQUIREMENTS We are looking for0-2yearsof experience in accounts receivable follow-up/denial management for US healthcare customers Fluent verbal communication abilities / call centre expertise Knowledge of Denials management and A/R fundamentals will be preferred Willingness to work continuously on night shifts Basic working knowledge of computers. Prior experience working in a medical billing company and using medical billing software will be considered an advantage. Knowledge of Healthcare terminology and ICD/CPT codes will be considered a plus Willingness to work from the office. Looking for Immediate Joiner. Freshers can also apply

Good knowledge in Electronics hardware. Knowledge of Cadence sch capture and PCB design tools. Good knowledge of Circuit Theory and Electronic Devices Should have good hardware design and development knowledge (requirements definition, design, reviews, testing etc). Design knowledge in Analog and Digital Circuits Digital design experience including micro-controllers, SPI, I2C, RS232,RS422, Ethernet etc. Analog design experience including active passive filters, amplifiers is helpful. Capable of conceptual design, parts selection, design simulation, detailed design, schematic capture and PCB design rules creation. Should be able to troubleshoot embedded boards/systems. Capable of writing supporting documentation to coordinate and establish layout practices and test procedures for the current design. Hands-on experience on using Lap tools like multimeter , Digital oscilloscope , spectrum analyzer , power supply etc Design knowledge in analog and digital video interfacing will be a plus point. Design knowledge on EMI/ EMC will be a plus point. Good to have knowledge in c programming Good written & verbal communication skills.Role and responsibility Responsible for the design and development of new products as well as the support and modification of existing products. Coordinate with layout teams to monitor correct guidelines are being followed. Manage prototype builds with contract manufacturers. Review Execute test protocols and document results. Support the boards and systems during environmental testing and entry into production. Be integral part of the Hardware Design Team as a driver of new ideas as well as provider of feedback for improvement of existing products. Continuous interaction with other departments (Software, Mechanical, etc) as part of daily board design practices and to support & maintain inter-departmental communications. Support board layout as well as board and system level bring-up, debug and verification. Involvement in customer support activities by site visits/giving demos /training /installation/solving customer's field issues is essential

Good Knowledge of Allegro PCB Editor Ver 16.6 & 17.2 Tool and ORCAD Capture Tool - Complete understanding of PCB Layout process with knowledge of IPC standards - Design of Single Sided, Double sided and multilayer boards - Expertise in design of high-speed digital, Analog, Power circuits, RF & video signals, and design for EMI/EMC - PCB's Footprint (Decal) Creation as per IPC Standard - Knowledge about Signal integrity, EMC/EMI, Power integrity - Good sound understanding in BGA Routing with Blind ,Buried and micro via concept. - Should have knowledge of rigid flex PCB design - Good knowledge on Electronics Component - Sound familiarity with fabrication and assembly process - Should have a sound understanding of the DFM process for PCB - Basic circuit design knowledge

Job Description

Role:                    : .NET Full Stack Developer

Designation      : Software Engineer / Sr. Software Engineer

Location:            : Ahmedabad

 

About the Team

An established IT Product & Engineering team following agile development principles, automated deployments, multiple staging environments. You will be joining experienced team of senior developers, UX/UI designers, DevOps, QA, product & project managers. Using various technologies and applications fully hosted on cloud.

 

Experience

• 6 to 12 years of experience in .Net technologies
• At least 2 years of hands-on experience designing & developing medium to large scale applications with Front-End JavaScript Frameworks, preferably Angular
• Well versed with advanced programming concepts of both front-end and back-end technologies

Responsibilities

• As a Software Engineer Professional, you will be responsible for the development, implementation, and maintenance of applications, using C#, .Net Core, NodeJS, Angular and ElectronJS, SQL, NoSQL and various other technologies.
• Develop high quality and reliable code with unit test cases, meeting given specifications.
• Develop front-end user interfaces using Angular.
• Implement back-end services and APIs using C# and .Net, .NET Core.
• Optimize application performance and ensure scalability.
• Collaborate with engineering, product team and UI/UX to deliver best products.
• Follow outlined standards of quality related to code and systems.
• Have a strong customer focus.

Essential Skills – Abilities

• Proven experience as a Full Stack Developer or similar role
• Strong Experience in C#, MVC and WEB API, Database Design and SQL queries using SQL server
• Experience in Angular
• Good Experience in .Net Core
• Ability to self-learn and deliver with minimal help / supervision
• Must have excellent communication & presentation skills.
• Good analytical and problem-solving skills

Value Add:

• Prior eCommerce industry domain experience
• Micro Front End Architecture
• NgRx for State Management
• NodeJs, Electron JS, PostgreSQL, Mongodb, Elasticsearch, Kafka, Redis, AngularJs (nice to have)
• Experience in Docker, Kubernetes
• Experience with working on highly scalable applications running as microservices on AWS / Azure.

Perks

•  Work-life balance & Flexible working hours. 5 days a week.
•  Every minute you work is paid.
•  Hybrid working facilities.
•  Mediclaim Insurance & Accidental death Insurance coverage
•  Employee referral bonus scheme.
•  28 days holidays (up to 35 depending on years of service). No Sandwich leave policy.
•  Enjoyable atmosphere, fast-Paced, fun, and creative space.
•  Canteen full of fruits & beverages
•  Learning & Development Opportunities

Skills:- .NET, ASP.NET, Angular (2+), Javascript, MVC Framework, SQL server, Object Oriented Programming (OOPs) and Design patterns

Tonbo Imaging is searching for a highly qualified Chartered Accountant with expertise in indirect taxation to join our team as an Indirect Taxation Specialist. This role will be pivotal in managing all aspects of indirect taxation for the company, ensuring compliance with applicable laws and regulations while optimizing tax efficiency. The ideal candidate will possess at least five years of experience in indirect taxation, with a strong understanding of GST, customs duties, and other indirect tax matters.Responsibilities:Develop and implement strategies to optimize the company's indirect tax position, including GST, customs duties, and other indirect taxes.Ensure compliance with all relevant indirect tax laws and regulations, including timely and accurate filing of GST returns, customs declarations, and other required documentation.Monitor changes in indirect tax laws and regulations and assess their impact on the company, providing recommendations for compliance and tax optimization.Collaborate with internal teams, including finance, procurement, and logistics, to ensure indirect tax implications are considered in business operations and transactions.Review contracts, agreements, and other documents to identify potential indirect tax implications and provide guidance on structuring transactions tax efficiently.Assist with indirect tax audits and inquiries, including preparing documentation and responding to queries from tax authorities.Provide guidance and training to internal stakeholders on indirect tax matters and compliance requirements.Conduct periodic reviews and audits of indirect tax processes and controls to ensure accuracy and compliance with policies and procedures.Stay updated on industry trends and best practices in indirect taxation and leverage this knowledge to continuously improve the company's tax processes and procedures.Qualifications:Bachelor's degree in Accounting, Finance, or a related field. Master's degree or CPA certification is a plus.Chartered Accountant (CA) qualification is required.Minimum of five years of experience in indirect taxation, with a strong understanding of GST, customs duties, and other indirect tax matters.Thorough knowledge of indirect tax laws, regulations, and compliance requirements.Experience with indirect tax software and ERP systems.Excellent analytical and problem-solving skills, with a keen attention to detail.Strong communication skills, with the ability to effectively communicate complex tax concepts to non-tax professionals.Ability to work independently and as part of a team, with strong organizational and time management skills.Proactive mindset with a commitment to continuous learning and professional development.Join Tonbo Imaging and play a key role in managing our indirect taxation functions, ensuring compliance and optimizing our tax position. If you have the qualifications and experience we're looking for, we invite you to apply and become part of our dynamic team.

Varex Imaging, headquartered in Salt Lake City, USA, is a leading innovator, developer, and manufacturer of X-ray imaging component solutions, which includes X-ray tubes, digital flat panel detectors, software, and other key components of X-ray imaging systems. With a 70+ year history of successful innovation, you will find our components in numerous medical, industrial, and security imaging applications worldwide. Let us start with making the invisible visible for you…We have started our India manufacturing operations with a brownfield setup and are just a step away from establishing our own greenfield manufacturing setup. For this new and exciting chapter of Varex, we are looking for highly motivated people to help us to succeed in our business operations in India.We are looking for an Application System Engineer for our flat panel detector business in Visakhapatnam. This position will collaborate with the team in the Salt Lake City and is expected to work within the same working hours as the rest of the team. The role of the applications team is to help new customers integrate Varex products into the customers systems. We do this by providing technical support to our customer’s engineering team that is doing this integration. This involves helping the customer use our software API to interface to the detector and helping the customer develop the hardware synchronization between the detector and the generator. Your RoleProvide Technical Expertise through sales presentations, product demonstrations and maintanence of company products. Assist the sales staff in assessing potention applications of company products to meet customer needs Building mini applications to demostrate feasibility of the customer requirements Provide software development and consultation to prospective users and help our customers develope the SW interface with our detector. Help the customer troubleshoot issues with the interface between our detector and their system Act as an interface between the customer’s technical team and the Varex technical team Your Profile A degree in Electrical Engineering, Computer Science or equivalent 5 years' experience working in Medical Industry Excellent communication skills in English Cross-functional collaboration with different teams, and stakeholders globally Experience working with radiographic and fluoroscopic medical systems What we offer A unique opportunity to become part of growing organization in India being part of a global market leader in Xray imaging components. Excellent development potential An international work environment with global teams collaborating on various projects across several countries. Competitive compensation package including participation in Varex incentive plans Corporate Health Benefits Additional benefits will be added as we grow Next steps If your background aligns with this role, our Talent Acquisition Specialist will reach out to you. Following confirmation of a match, you'll have an exciting opportunity to meet with the hiring manager based in Salt Lake City. This meeting will provide valuable insights into our company and allow you to ask any questions you may have. Ready to shape the future of X-ray imaging and make an impact in the industry? Please submit your application, along with your preferred salary request, through our recruitment portal on Workday at your earliest convenience. We are actively interviewing potential candidates as applications are received. We will promptly advance with the most promising candidates. Please note that you must press save before submitting your CV. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or on the basis of disability.

Qualifications:Bachelor's or Master's degree in Electrical Engineering, Computer Engineering, or related field.Proven experience in FPGA design and development, including VHDL or Verilog programming.Strong understanding of digital signal processing (DSP) concepts and algorithms.Hands-on experience with FPGA development tools and platforms (e.g., Xilinx Vivado, Intel Quartus).Proficiency in image processing techniques such as filtering, feature extraction, and object recognition.Familiarity with industry-standard interfaces and protocols (e.g., PCIe, Ethernet, HDMI).Experience with hardware description languages (HDL) and simulation tools (e.g., ModelSim, Questa).Excellent problem-solving skills and attention to detail.Ability to work effectively in a collaborative team environment.Strong written and verbal communication skills.Preferred Qualifications:Experience with high-speed data processing and parallel computing architectures.Familiarity with machine learning techniques and frameworks for image processing.Knowledge of embedded systems design and development.Understanding of optimization techniques for FPGA-based systems.Experience working in the defense or aerospace industry.

OverviewWe are currently seeking a skilled Software Development Engineer in Test (SDET) with a strong background in software quality assurance. This role requires writing unit and integration test cases, executing system tests, and setting up automated testing suites. The ideal candidate will be proficient in C or C++ and have experience in the avionics or automotive industries, especially in safety-critical systems. Familiarity with DO-178C standards is a major plus. The position also involves occasional travel to client locations to understand their requirements and ensure alignment with our testing strategies.ResponsibilitiesTest Case Development: Design and maintain effective unit and integration test cases using C or C++.Automated Testing: Develop and manage automated test suites to ensure high-quality software delivery.System Testing: Conduct comprehensive testing of software systems to detect and resolve issues.Compliance and Standards: Adhere to DO-178C standards, particularly in the context of avionics or automotive safety-critical systems.Client Interaction: Travel to client locations as needed to collaborate, gather requirements, and provide testing expertise.Collaboration and Communication: Work closely with development teams and stakeholders to align testing strategies with business objectives.Documentation: Document all test cases, results, and identified issues meticulously.QualificationsBachelor’s degree in Computer Science, Software Engineering, or related field.Demonstrable experience in software testing, particularly in writing test cases in C or C++.Proficiency in automated testing tools and frameworks.Experience with DO-178C standards, especially in safety-critical systems in the avionics or automotive sectors.Willingness to travel to client sites as required.Strong problem-solving, analytical, and debugging skills.Excellent communication and teamwork abilities.

Good knowledge in Electronics hardware.Knowledge of Cadence sch capture and PCB design tools.Good knowledge of Circuit Theory and Electronic DevicesShould have good hardware design and development knowledge (requirements definition, design, reviews, testing etc).Design knowledge in Analog and Digital CircuitsDigital design experience including micro-controllers, SPI, I2C, RS232,RS422, Ethernet etc.Analog design experience including active passive filters, amplifiers is helpful.Capable of conceptual design, parts selection, design simulation, detailed design, schematic capture and PCB design rules creation.Should be able to troubleshoot embedded boards/systems.Capable of writing supporting documentation to coordinate and establish layout practices and test procedures for the current design.Hands-on experience on using Lap tools like multimeter , Digital oscilloscope , spectrum analyzer , power supply etcDesign knowledge in analog and digital video interfacing will be a plus point.Design knowledge on EMI/ EMC will be a plus point.Good to have knowledge in c programmingGood written & verbal communication skills. Role and responsibility Responsible for the design and development of new products as well as the support and modification of existing products.Coordinate with layout teams to monitor correct guidelines are being followed.Manage prototype builds with contract manufacturers.Review Execute test protocols and document results.Support the boards and systems during environmental testing and entry into production.Be integral part of the Hardware Design Team as a driver of new ideas as well as provider of feedback for improvement of existing products.Continuous interaction with other departments (Software, Mechanical, etc) as part of daily board design practices and to support & maintain inter-departmental communications.Support board layout as well as board and system level bring-up, debug and verification.Involvement in customer support activities by site visits/giving demos /training /installation/solving customer's field issues is essential