bio medical technician

Fatima Memorial Hospital

Job Responsibilities:<ul><li>Installation, testing, and maintenance of medical equipment</li><li>Troubleshooting and repair of biomedical devices</li><li>Preventive maintenance of hospital equipment</li><li>Calibration and safety checks of medical machines</li><li>Support clinical staff in proper use of equipment</li><li>Maintain equipment service records and documentation</li></ul>Qualification Required:<ul><li>Diploma of Associate Engineering (DAE) Biomedical / Electronics</li></ul>Experience:<ul><li>Fresh or 1&ndash;3 years&rsquo; experience in hospital biomedical equipment maintenance (preferred)</li></ul>Skills Required:<ul><li>Good knowledge of Microsoft Excel (data entry, record keeping, reporting)</li><li>Good communication and teamwork</li><li>Ability to work in hospital environment</li></ul>Education:<ul><li>Master's (Required)</li></ul>Experience:<ul><li>Biomedical Engineer: 2 years (Required)</li><li>Biomedical Technician: 3 years (Required)</li></ul>Work Location: In person

Biomedical Technician

TRIMEDX

<div>If you are wondering what makes TRIMEDX different, it's that all of our associates share in a common purpose of serving clients, patients, communities, and each other with equal measures of care and performance.<ul><li>
Everyone is focused on serving the customer and we do that by collaborating and supporting each other</li><li>
Associates look forward to coming to work each day</li><li>
Every associate matters and makes a difference</li></ul>
It is truly a culture like no other &mdash; We hope you will join our team! Find out more about our company and culture here.
Summary
The Biomedical Technician II (BMET II) is required to install, inspect, troubleshoot, repair, calibrate, and verify the performance of complex biomedical equipment with minimal supervision. The individual should be competent in the use of all applicable test equipment and tools required in the performance of these duties. The BMET II may serve as technical advisor to the medical and clinical staff in the safe operation and use of clinical equipment. This position also assists in developing specifications for the selection of new clinical equipment. The individual demonstrates adherence to the TriMedx core values in all professional interactions by showing respect to all people, creating real value, initiating meaningful change, and exhibiting integrity.
Responsibilities
Technical Service &ndash; 40%<ul><li>
Perform performance assurance (PA) inspections, scheduled maintenance, electrical safety inspections (ESI), and operation verification procedures (OVP) on complex and intricate biomedical equipment</li><li>
Repair, install, and calibrate complex and intricate biomedical equipment</li><li>
Inform supervisors of the status of repairs, scheduled inspections, unusual equipment situations, and any customer concerns</li><li>
Work with, direct, and document the activities of subcontractors, vendors, and outside service technicians to ensure proper service delivery</li><li>
Maintain biomedical expertise through ongoing training and education</li><li>
Assist with Service Operations Special Projects as assigned</li></ul>
Regulatory Compliance &ndash; 25%<ul><li>
Ensure the accuracy and integrity of the equipment database to include the inventory, performance assurance (PA) schedules, nomenclature, and service history</li><li>
Adheres to the Medical Equipment Management Plan (MEMP), including all regulatory agency compliances and other applicable policies and procedures</li><li>
Responsible for ensuring all service and documentation is complete, timely, and accurate</li></ul>
Account Relationship Management &ndash; 25%<ul><li>
Build and maintain customer relationships</li><li>
Discuss equipment status and functionality with clinicians</li><li>
Adheres to the Mission, Vision, and Values of the organization(s) served.</li><li>
Provide a positive representation of TriMedx services by integrating the core values into job performance</li></ul>
Inventory &ndash; 10 %<ul><li>
Perform periodic inspections of current inventory status</li><li>
Verify the completion of security analysis for new customer equipment</li><li>
Performs Incoming Inspections (II) to maintain a complete and accurate inventory of medical devices, including trial and evaluation, rental, and loaner equipment in addition to permanently assigned equipment inventory.</li><li>
Maintain the accuracy and integrity of the equipment database to include inventory, performance assurance (PA) schedules, nomenclature, and service history</li><li>
Make recommendations regarding inventory</li></ul>
All other duties as assigned
Skills and Experience<ul><li>
Complex computer skills including the ability to administrate a system, interpret error codes, defragment hard-drives, replace power supplies, and interpret computer codes required</li><li>
Ability to integrate information from a variety of sources</li><li>
Excellent interpersonal and customer service skills</li><li>
Strong written, verbal, and presentational communication skills</li><li>
Valid driver&rsquo;s license required; variable travel requirements depending on primary site that may require use of personal vehicle</li></ul>
Education and Qualifications<ul><li>
2 year degree in a technical/electronics field or equivalent experience required. This requirement will be waived if the applicant has received the TRIMEDX Trained Certification or completed an equivalent biomedical related certification program.</li><li>
Technical Certification (CBET) strongly preferred</li><li>
Minimum 3 years&rsquo; experience working with biomedical equipment in a clinical engineering environment</li><li>
Travel may be required based on customer or business needs</li></ul>
At TRIMEDX, we are committed to cultivating a workplace culture where every associate feels valued, supported, and empowered to thrive. This culture reflects our belief that our people are our foundation, their well-being is essential, and shared success is built through meaningful work, recognition, and opportunities for growth.
We embrace people&rsquo;s differences which include age, race, color, ethnicity, gender, gender identity, sexual orientation, national origin, education, genetics, veteran status, disability, religion, beliefs, opinions and life experiences.
Visit our website to view our Workplace Culture Commitment , along with our social channels to see what our team is up to: Facebook, LinkedIn, Twitter. 
TRIMEDX is an Equal Opportunity Employer. Drug-Free Workplace.
Because we are committed to providing a safe and productive work environment, TRIMEDX is a drug-free workplace. Accordingly, Associates are prohibited from engaging in the unlawful manufacture, sale, distribution, dispensation, possession, or use of any controlled substance or marijuana, or otherwise being under the influence thereof, on all TRIMEDX and Customer property or during working/on-call hours.</div>

Biomedical Technician II

<div>If you are wondering what makes TRIMEDX different, it's that all of our associates share in a common purpose of serving clients, patients, communities, and each other with equal measures of care and performance.<ul><li>
Everyone is focused on serving the customer and we do that by collaborating and supporting each other</li><li>
Associates look forward to coming to work each day</li><li>
Every associate matters and makes a difference</li></ul>
It is truly a culture like no other &mdash; We hope you will join our team! Find out more about our company and culture here.
Summary
The Biomedical Equipment Technician I (BMET I) provides clinical equipment services under the close supervision of TriMedx management. Duties include, but are not limited to, validation and inspection of clinical equipment for completeness, mechanical and electrical safety, and proper operation. The individual also performs planned maintenance inspections, calibrations, and repairs of general biomedical equipment. The BMET I assists other technicians in the troubleshooting and major repair of complex equipment. The individual demonstrates adherence to the TriMedx core values in all professional interactions by showing respect to all people, creating real value, initiating meaningful change, and exhibiting integrity.
Responsibilities
Technical Service &ndash; 40%<ul><li>
Perform performance assurance (PA) inspections, scheduled maintenance, electrical safety inspections (ESI), and operation verification procedures (OVP) on general biomedical equipment</li><li>
Repair, install, and calibrate general biomedical equipment</li><li>
Inform supervisors of the status of repairs, scheduled inspections, unusual equipment situations, and any customer concerns</li><li>
Work with, direct, and document the activities of subcontractors, vendors, and outside service technicians to ensure proper service delivery</li><li>
Maintain biomedical expertise through ongoing training and education</li><li>
Assist with Service Operations Special Projects as assigned</li></ul>
Regulatory Compliance &ndash; 25%<ul><li>
Ensure the accuracy and integrity of the equipment database to include the inventory, performance assurance (PA) schedules, nomenclature, and service history</li><li>
Adhere to the Medical Equipment Management Plan (MEMP), including all regulatory agency compliances and other applicable policies and procedures</li><li>
Responsible for ensuring all service and documentation is complete, timely, and accurate</li></ul>
Account Relationship Management &ndash; 25%<ul><li>
Build and maintain customer relationships</li><li>
Discuss equipment status and functionality with clinicians</li><li>
Adheres to the Mission, Vision, and Values of the organization(s) served.</li><li>
Provide a positive representation of TriMedx services by integrating the core values into job performance</li></ul>
Inventory &ndash; 10 %<ul><li>
Perform periodic inspections of current inventory status</li><li>
Verify the completion of security analysis for new customer equipment</li><li>
Performs Incoming Inspections (II) to maintain a complete and accurate inventory of medical devices, including trial and evaluation, rental, and loaner equipment in addition to permanently assigned equipment inventory.</li><li>
Maintain the accuracy and integrity of the equipment database to include inventory, performance assurance (PA) schedules, nomenclature, and service history</li><li>
Make recommendations regarding inventory</li><li>
All other duties as assigned</li></ul>
Skills and Experience<ul><li>
Complex computer skills including the ability to interpret error codes, defragment hard-drives, replace power supplies, and interpret computer codes required</li><li>
Ability to integrate information from a variety of sources</li><li>
Excellent interpersonal and customer service skills</li><li>
Strong written and verbal communication skills</li><li>
Valid driver&rsquo;s license required; variable travel requirements depending on primary site that may require use of personal vehicle</li></ul>
Education and Qualifications<ul><li>
2 year degree in a technical/electronics field or equivalent experience required. This requirement will be waived if the applicant has received the TRIMEDX Trained Certification or completed an equivalent biomedical related certification program.</li><li>
3 months experience working with biomedical equipment in a clinical engineering environment preferred</li><li>
Travel may be required based on customer or business needs</li></ul>
At TRIMEDX, we are committed to cultivating a workplace culture where every associate feels valued, supported, and empowered to thrive. This culture reflects our belief that our people are our foundation, their well-being is essential, and shared success is built through meaningful work, recognition, and opportunities for growth.
We embrace people&rsquo;s differences which include age, race, color, ethnicity, gender, gender identity, sexual orientation, national origin, education, genetics, veteran status, disability, religion, beliefs, opinions and life experiences.
Visit our website to view our Workplace Culture Commitment , along with our social channels to see what our team is up to: Facebook, LinkedIn, Twitter. 
TRIMEDX is an Equal Opportunity Employer. Drug-Free Workplace.
Because we are committed to providing a safe and productive work environment, TRIMEDX is a drug-free workplace. Accordingly, Associates are prohibited from engaging in the unlawful manufacture, sale, distribution, dispensation, possession, or use of any controlled substance or marijuana, or otherwise being under the influence thereof, on all TRIMEDX and Customer property or during working/on-call hours.</div>

Biomedical Technician I

Biomedical Technician l

QPS Holdings, LLC

<div>The Clinical Research Technician position offers flexible hours and a rewarding work environment in the drug research field. This position is primarily responsible for monitoring the study volunteers and ensuring the clinical study is being recorded, conducted, and reported in agreement with the study requirements. This position offers variety, and no two days are alike. The hours are scheduled on an as needed basis and can range from 0-29 hours per week. The essential duties are:<ul><li>
Read and understand study documents, time and events, study restrictions and expectations of sponsor.</li><li>
Check in/out study volunteers and monitor their behavior for study compliance, safety, adverse events and concerns.</li><li>
Perform essential study duties such as recording mealtimes, performing vitals and recording results.</li><li>
Review raw data to ensure accuracy.</li><li>
Help to supervise events to ensure studies are done on time and in accordance with SOPs and Protocols.</li><li>
Maintain cleanliness of the clinics and all study-related areas.</li></ul>
Experience<ul><li>
High school diploma or equivalent</li><li>
Outstanding customer service skills</li><li>
High attention to detail</li><li>
Ability to work weekends is desirable</li><li>
Ability to work flexible hours</li></ul>
Please visit Recruitment (adp.com) to apply for this position through the company website. 
QPS Bio-Kinetic (BKCA) provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, QPS Bio-Kinetic (BKCA) complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.</div>

Clinical Research Technician

Bio-Techne

<div>By joining Bio-Techne, you&rsquo;ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.
Pay Range:
$55,600.00 - $91,450.00
Position Summary:
Are you passionate about science and have experience in quality assurance related activities? This could be the opportunity for you! To join a company that develops and provides a unique and cutting edge lineup of products and tools used by life science researchers, pharma, and diagnostic companies to make scientific discoveries, medical breakthroughs, understand the cause of diseases, develop new treatments, and much more!
As a Quality Assurance (QA) Specialist you will support the quality functions of Bio-Techne through quality systems development and improvement, document and records review, auditing, and other quality functions. The QA Specialist will understand and follow appropriate quality procedures to meet compliance standards, including ISO 9001, ISO 13485, and 21CFR820.
Key Responsibilities:
<ul><li>Participate in cross-functional team meetings as a quality representative, assist in management of quality issues and offer input representing quality assurance (new product design, data reviews or root cause investigations).
</li><li>Work collaboratively with all functions to ensure understanding and conformance with quality requirements.
</li><li>Assist in Quality review of newly written or revised GMP specifications, documents, labels and literature for accuracy and completeness. Write documents as needed.
</li><li>Assist in Quality review of batch records for product manufacturing.
</li><li>Assist in monitoring quality systems through monthly complaint meetings, monthly reports, trending, and annual quality review.
</li><li>Assist in writing or reviewing newly written or revised validation plans and review the completed validations for accuracy and completeness.
</li><li>Assist in maintaining and/or developing companywide Quality systems including, but not limited to, quality audits, product validation, document control, acceptance activities, production and process control, and corrective and preventive action.
</li><li>Follows company policies and practices as outlined in the Handbook and follows guidelines regarding safety as outlined in the AWAIR, Chemical Hygiene and Exposure Control manuals in accordance with the job.
</li><li>Follows applicable standard operating procedures (SOPs), including a good understanding of quality associated SOPs.
</li><li>Propose process improvements and areas for improvement to supervisor.
</li><li>Conduct inspections of raw materials, intermediates, and finished goods to ensure specifications and quality standards are met.
</li><li>Conduct inspection of product literature and labels to ensure accuracy.
</li><li>Performs additional duties as assigned.
</li></ul>Job Qualifications
Education and Experience:
<ul><li>This position requires a minimum of a bachelor&rsquo;s degree in a biological or chemical scientific discipline, with 1 - 3 years of related experience in quality activities in a science related field, or equivalent combination of education and experience.
</li><li>Must have the ability to work in a fast-paced environment with an attention to detail, organization, and time management skills. Should be able to work individually, but also as a contributing member of internal and cross-functional teams maintaining good communication skills, both verbally and in writing.
</li><li>Experience and understanding of ISO 9001 or ISO 13485 is preferred.
</li></ul>Knowledge, Skills, and Abilities:
<ul><li>Attention to detail and organizational skills are required
</li><li>Working knowledge of Microsoft Word and Excel are required
</li><li>Computer entry, typing, or electronic document filing skills are require
</li><li>Must be able to work in a fast-paced environment where multitasking is required
</li><li>Must have excellent verbal and written communication skills
</li><li>Knowledge of technical, regulatory, quality and production management systems
</li><li>Knowledge of documentation principles and processes
</li><li>Skills in accuracy, clarity, and proofreading
</li><li>Skills in problem solving, root cause analysis, and appropriately evaluate a course of actions
</li></ul><div><div><div><div>Why Join Bio-Techne:
<ul><li><h3 class="jobSectionHeader">We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
</h3></li><li><h3 class="jobSectionHeader">We invest in our employees&rsquo; financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
</h3></li><li><h3 class="jobSectionHeader">We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
</h3></li><li><h3 class="jobSectionHeader">We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging.
</h3></li><li><h3 class="jobSectionHeader">We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
</h3></li><li><h3 class="jobSectionHeader">We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.
</h3></li></ul>Bio-Techne is an E-Verify Employer in the United States.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.</div></div></div></div></div>

Advanced Quality Assurance Specialist

Piedmont Healthcare

<div>Overview:

At Piedmont Healthcare, you&rsquo;ll love a shared purpose, be motivated to be your best, and be recognized for your contributions. Piedmont Healthcare leaders are in your corner and invested in your success. Our wellness programs and comprehensive total benefits and rewards will meet your needs for today and help you plan for the future.
Responsibilities: Receiving, logging, dispatches, and tracks calls on diagnostic imaging related service issues. Creating requisition for invoice payments, database keypunch and customer service follow up. Ensuring that assistance is provided to the end user community as quickly and efficiently as possible Qualifications:

Education<ul><li>
H.S. Diploma or General Education Degree (GED) Required</li><li>
Associate&rsquo;s Degree Preferred</li></ul>
Work Experience<ul><li>
2 years experience in customer service field, or other related field Required</li></ul>
Business Unit : Company Name: Piedmont Healthcare Corporate</div>

Biomed Engineering Dispatcher

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