clinical engineer

Brown University Health

<div>SUMMARY: Reports to Director of Medical Engineering and is responsible for capital equipment evaluation, selection, planning and installation, integration, interconnectivity of medical devices and systems. Plans and organizes Brown University Health system-wide Medical Equipment Management Plan to ensure patient safety and safe and quality operations of medical devices and meet regulatory agencies requirements. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another. In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include: Instill Trust and Value Differences Patient and Community Focus and Collaborate RESPONSIBILITIES: PRINCIPAL DUTIES AND RESPONSIBILITIES: Designs and develops processes and methodologies to evaluate state-of-the-art capital equipment. Coordinates the selection, acquisition and installation of new Patient care technology systems. Interacts with outside vendors, regulatory agencies and personnel of various levels within and outside of Brown University Health system to provide consultation on performance, technical specifications, clinical applications, evolving compatibility and safety of Medical Devices and systems. Develops, standardizes and implements system-wide Medical Equipment Management Plan to ensure safe and quality performance of medical equipment, and meeting the Environment of Care Committee requirements at each Brown University Health affiliate. Participates in organizational failure modes and effects analysis as requested in compliance with TJC requirement. Performs technical testing of equipment performance and participates in root cause analysis on equipment failure and incidents in compliance with Safe Medical Device Act (SMDA). Continually reviews Medical device systems and components to determine which are technologically obsolete or otherwise no longer adequately supportable and prepare multi-year replacement plans and implements component and Medical device system upgrades in a timely manner. Coordinates with various stakeholders a process to standardize, prioritize, develop and implement plans to manage/mitigate risks associated with interconnectedntegrated Medical device systems by applying appropriate administrative, Physical and technical safeguards. Performs Failure Modes and Effectiveness Analysis (FMEA) on Medical devices and systems connected to IT networks to identify points of failure. Monitors and adopts industry Best Practices to insure integrity, availability and confidentiality of data maintained and transmitted across interconnected and integrated Medical devices and systems. Educates various project stakeholders on implications associated with the proliferation of interconnected and integrated medical device systems and technologies. Provides technical oversight and consultation to Medical Engineering and other Clinical/Non-Clinical Staff as required in clinical device systems implementation and integration projects. Develops equipment performance improvement standards and corrective action measures to ensure compliance with regulatory standards related to medical devices. Ensures that system wide Medical Equipment Maintenance policies, procedures and required records are in compliance with safety codes set out by regulatory agencies such as Food and Drug Administration (FDA), Department of Public Health (DPH), National Fire Protection Association (NFPA), National Electrical Code (NEC), The Joint Commission and manufacturers' requirements. Maintains the integrity of FDA Approval for interconnectedntegrated medical systems including Medical Device Data Systems (MDDS). Responsible for the standardization of the Medical Engineering department performance standards, procedures and protocols, maintenance procedures and system-wide problem solving and communication. Coordinates the internal and external medical device product recalls and alerts to ensure safe environment for patients, staff and visitors that are part of all Medical Engineering departments system-wide. Investigates equipment incidents related to Medical/legal issues and works closely with Risk Management and the Legal Department within the hospital. Manage and Plan the Wireless Radio Frequency spectrum in the hospital environment to reduce the risk of Electro Magnetic Interference (EMI) and ensure safe performance of the Wireless Medical devices. Manages the computerized medical equipment management system. Maintains a very detailed and current inventory of networked and integrated medical systems including catalogue of services, features and interconnections. Streamlines the equipment database to ensure it is up to date from a regulatory standards point of view. Works with the Medical Equipment Management database vendor to improve user interfaces, resolve programming issues, create custom interfaces (forms, reports etc.) to improve database functionality and reflect the changes in staff/departmental processes. Participates in performance improvement initiatives and demonstrates the use of Engineering principles and analytical concepts for quality improvement in daily operations Trains/Mentors Clinical, Non-Clinical and Medical Engineering staff in the safe and effective MINIMUM QUALIFICATIONS: BASIC KNOWLEDGE: Bachelor's degree in Biomedical or other engineering discipline with one to two years of experience working in Clinical Engineering operations or similar environment is required. A Masters' Degree in Biomedical Engineering with Clinical Engineering concentration (track), or a Masters' Degree in Biomedical Engineering with prior work experience as a Clinical Engineer in a healthcare setting is preferred. EXPERIENCE: Experience in a healthcare environment or as gained through a hospital based internship program as needed for the degrees noted above. If qualifying based on prior work experience, knowledge of medical device systems and technologies used in a healthcare environment which includes principles of operation, major features, device networking, methods for testing, and evaluating each technology available in the market. This includes a required knowledge of human physiology and anatomy which relates to understanding the engineering principles in the application of clinical devices and technologies in complex medical devices which may include and are not limited to Diagnostic and Therapeutic radiology equipment, automated lab equipment, central patient monitoring systems, anesthesia machines, surgical lasers, microscopes, video systems and integration is required. Knowledge of codes and standards of FDA, JCAHO and other regulatory organizations governing the technology management in a health care environment. Knowledge of database programming languages including Microsoft SQL and Access; XML, HTML and VB. Must be proficient in personal computer applications including word processing and spreadsheets as well as technical drawing software including Microsoft Project and Visio. Strong communication and team building skills with leadership qualities. Proven ability to work collaboratively within a multidisciplinary consulting team environment as this position will lead interdisciplinary teams and manage complex projects. WORK ENVIRONMENT ANDPHYSICAL REQUIREMENTS: Exposed to normal patient care environment with frequent standing and walking. INDEPENDENT ACTION: Performs independently within the department's policies and practices. Refers specific complex problems to the supervisor when clarification of the departmental policies and procedures are required. SUPERVISORY RESPONSIBILITY: None
Pay Range:
$69,732.94-$115,039.29
EEO Statement:
Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment. 
Location:
593 Eddy Street - Gerry House - N/A Providence, Rhode Island 02903
Work Type:
7:30am-4:00pm
Work Shift:
Day
Daily Hours:
8 hours
Driving Required:
No</div>

Clinical Engineer

Dr. Ziauddin Hospital

Education:Bachelor in Biomedical EngineerExperience:02 to 03 years of relevant experienceResponsibilities:<ul><li>Biomedical engineers apply engineering principles to repair and replace medical equipment.</li><li>Responsible for performing equipment repair and maintenance to ensure smooth running of all clinical equipment in the hospital.</li><li>Maintains biomedical/ Dialysis equipment by completing preventive maintenance schedules, troubleshooting and repairing malfunctions.</li><li>Discusses and solves problems with manufacturing and purchasing departments.</li></ul>Job Type: Full-timeJob Type: Full-timeWork Location: In person

Biomedical Engineer

OMI Hospital

Are you a passionate Biomedical Engineer with hands-on experience in the maintenance and calibration of medical equipment. Join our dedicated healthcare team and play a vital role in ensuring the safety, functionality, and innovation of clinical technology.Key Responsibilities:<ul><li>Install, maintain, troubleshoot, and repair medical equipment and systems.</li><li>Perform routine inspections and preventive maintenance of biomedical devices.</li><li>Ensure compliance with hospital safety standards and healthcare regulations.</li><li>Collaborate with clinical and technical teams to assess equipment needs and upgrades.</li><li>Maintain detailed records of services and repairs conducted.</li></ul>Requirements:<ul><li>Bachelor&rsquo;s degree in Biomedical Engineering or a related discipline.</li><li>1&ndash;2 years of relevant experience in a hospital or healthcare environment.</li><li>Sound knowledge of diagnostic and therapeutic medical devices.</li><li>Ability to read technical manuals and schematics.</li><li>Strong problem-solving skills and attention to detail.</li><li>Good communication and teamwork abilities.</li></ul>Job Types: Full-time, ContractWork Location: In person

Bio Medical Engineer (Junior Level)

PhiMed

Job Overview The Biomedical Engineer will be responsible for ensuring the optimal performance, safety, and compliance of all medical equipment within the clinic. This includes preventive maintenance, troubleshooting, procurement evaluation, staff training, and coordination with suppliers and regulatory bodies. The role serves as the technical expert supporting clinical and operational teams to ensure all devices are used effectively, safely, and in accordance with healthcare standards.Key Responsibilities:- Conduct comprehensive training sessions for medical and nursing staff, ensuring proper handling, operation, and maintenance of medical equipment at the end-user level.- Evaluate new medical devices and technologies for procurement, preparing detailed technical reports and recommendations to support management decisions.- Investigate equipment issues to determine warranty coverage, manage warranty claims efficiently, and ensure timely servicing and repairs.- Implement regular monitoring and preventive maintenance programs to maintain optimal device performance, minimize downtime, and extend equipment lifespan.- Respond promptly to service calls, perform diagnostic assessments, and carry out repairs or troubleshooting while adhering to safety and manufacturer protocols.- Maintain accurate and up-to-date records of all medical devices, including maintenance logs, calibration reports, and service histories in compliance with industry and regulatory standards.- Liaise with relevant authorities to ensure all medical devices and equipment meet local regulatory and licensing requirements.- Maintain effective communication with procurement teams, suppliers, and end-users to provide technical insights, support purchasing activities, and ensure smooth operations across departments.- Oversee and maintain the performance, safety, and compliance of key medical equipment across various departments.Qualifications:- Bachelor&rsquo;s degree in Biomedical Engineering or a related field.- Minimum 3&ndash;5 years of experience in a clinical or hospital environment.- Strong knowledge of medical device standards, maintenance protocols, and regulatory compliance (Qatar MOPH / DHP preferred).- Excellent troubleshooting, analytical, and communication skills.- Ability to train staff and document equipment records in compliance with industry best practices.Job Type: Full-time

Amara Hospital

<ul><li>Installing and maintaining equipmentBiomedical engineers install, maintain, and troubleshoot medical equipment. They also ensure that equipment functions properly and is safe for use.</li><li>Training staffBiomedical engineers train healthcare professionals on how to use biomedical equipment properly</li><li>Working with other professionalsBiomedical engineers work with medical professionals, scientists, and patients to understand their needs and develop advanced healthcare technology.</li><li>Managing clinical trialsBiomedical engineers manage clinical trials of new medical products and devices.</li><li>Assessing risksBiomedical engineers assess the risks associated with medical devices and propose safety measures.</li><li>Developing new diagnostic toolsBiomedical engineers develop new diagnostic tools based on safety standards.</li></ul>Job Types: Full-time, PermanentPay: &#8377;30,000.00 - &#8377;45,000.00 per monthBenefits:<ul><li>Paid sick time</li><li>Provident Fund</li></ul>Work Location: In person

Senior Biomedical Engineer

Surana Hospital & Research Centre

<ul><li>Design and development: Create new medical devices, from software for equipment to complex products like artificial organs, prosthetics, and diagnostic machines.</li><li>Research: Conduct research to solve clinical problems and analyze data to develop innovative healthcare solutions.</li><li>Installation and maintenance: Install, maintain, and repair medical equipment to ensure it is functioning safely and effectively.</li><li>Evaluation and support: Evaluate the performance of existing medical equipment and provide technical support and training to healthcare professionals.</li><li>Documentation and compliance: Maintain detailed records and write technical reports, ensuring compliance with regulatory standards.</li></ul>Job Type: Full-timePay: &#8377;9,635.18 - &#8377;30,000.00 per monthBenefits:<ul><li>Health insurance</li></ul>Work Location: In person

Capgemini Engineering

<div></div><div><div><div><div>Choosing Capgemini means choosing a place where you&rsquo;ll be empowered to shape your career, supported by a collaborative global community, and inspired to reimagine what&rsquo;s possible. Join us in helping leading healthcare and life sciences organizations unlock the value of data and drive evidence-based, impactful research.
<h2 class="jobSectionHeader">Your Role
</h2>As a Statistical Programmer II at Capgemini, you will be responsible for programming and validating clinical trial data displays, datasets, and documentation in alignment with regulatory standards. You&rsquo;ll collaborate with cross-functional teams and contribute to the delivery of high-quality statistical outputs for clinical research.
<h3 class="jobSectionHeader">In this role, you will:
</h3><ul><li>Program tables, listings, and graphs for clinical study reports (CSRs).
</li><li>Develop customized data displays per statistical analysis plans (SAPs).
</li><li>Write code using Base SAS, SAS procedures, and standardized macros.
</li><li>Analyze protocols, SAPs, and shell templates to understand data structure.
</li><li>Perform data checks to ensure accuracy and integrity of displays.
</li><li>Create SAS datasets from clinical databases, including status and efficacy datasets.
</li><li>Prepare documentation for programs, datasets, and derived variables.
</li><li>Create project-specific macros and formats.
</li><li>Load and prepare client data for external transfers and imports.
</li></ul><h3 class="jobSectionHeader">Additional Responsibilities for SP II:
</h3><ul><li>Assist in tracking project timelines and deliverables.
</li><li>Lead and mentor junior programmers in daily activities.
</li><li>Communicate with clients regarding risks, issues, and potential delays.
</li></ul><h2 class="jobSectionHeader">Your Profile
</h2><ul><li>Bachelor&rsquo;s degree required; Master&rsquo;s degree in Biostatistics, Computer Science, Mathematics, or related field preferred.
</li><li>Strong SAS programming skills and understanding of clinical trial and drug development processes.
</li><li>At least 7 years of clinical or SAS programming experience (for SP II).
</li><li>Ability to manage multiple tasks and deliver high-quality outputs on time.
</li><li>Strong communication skills in English (verbal and written).
</li><li>Ability to work independently and collaboratively in dynamic environments.
</li><li>Understanding of data standardization and statistical reporting in clinical trials.
</li></ul><h2 class="jobSectionHeader">What You&rsquo;ll Love About Working Here
</h2>We value flexibility and support our employees with remote work options and adaptable schedules to maintain a healthy work-life balance. Our inclusive culture brings together diverse professionals committed to growth, innovation, and excellence. You&rsquo;ll have access to continuous learning opportunities and certifications in emerging technologies and methodologies.
<h2 class="jobSectionHeader">About Capgemini
</h2>Capgemini is a global business and technology transformation partner, helping organizations accelerate their dual transformation to address the evolving needs of customers and citizens. With a strong 55-year heritage and deep industry expertise, Capgemini is trusted by its clients to address the entire breadth of their business needs&mdash;from strategy and design to operations.
To achieve this, Capgemini draws on the capabilities of its 360,000 team members in more than 50 countries, all driven by the purpose of unleashing human energy through technology for an inclusive and sustainable future. It is a responsible and diverse organization with market-leading capabilities in digital, cloud, and data
Works in the area of Software Engineering, which encompasses the development, maintenance and optimization of software solutions/applications.1. Applies scientific methods to analyse and solve software engineering problems.2. He/she is responsible for the development and application of software engineering practice and knowledge, in research, design, development and maintenance.3. His/her work requires the exercise of original thought and judgement and the ability to supervise the technical and administrative work of other software engineers.4. The software engineer builds skills and expertise of his/her software engineering discipline to reach standard software engineer skills expectations for the applicable role, as defined in Professional Communities.5. The software engineer collaborates and acts as team player with other software engineers and stakeholders.</div></div></div></div>

Statistical Programming II

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