UNKNOWN

ADAPTED_NOW

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here (https://www.myworkday.com/umiami/d/task/1422$7248.htmld) to log in to Workday to use the internal application process. The Biomedical Technician 1 (H) performs a variety of routine tasks, including the installation, maintenance, calibration, and repair of biomedical equipment, under the supervision and guidance of a more experienced biomedical engineer.

Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here (https://www.myworkday.com/umiami/d/task/1422$7248.htmld) to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER_eRecruiting_ApplyforaJob.pdf) . Biomedical Technician The University of Miami/UHealth Department of Clinical Engineering has an exciting opportunity for a Temporary Full Time Biomedical Technician 1 to work at the UHealth Medical Campus. Core Summary The Biomedical Technician 1 (H) performs a variety of routine tasks, including the installation, maintenance, calibration, and repair of biomedical equipment, under the supervision and guidance of a more experienced biomedical engineer. Core Responsibilities + Utilizes standard and specialized electronic test equipment and tools. + Repairs, tests, and calibrates medical equipment according to OEM/AEM specifications in accordance with Joint Commission standards. + Assist in enforcing recall and safety alert programs for medical devices, including medical device hazard investigations. + Assures compliance with patient safety goals and applicable requirements. + Completes 100% of scheduled ITM’s assigned on a monthly basis. + Orders replacement parts and supplies necessary for the servicing of medical equipment. + Prioritizes workload effectively and completes all work assignments in a timely manner. + Maintains accurate documentation as required by current policies and procedures. + Adheres to University and unit-level policies and procedures and safeguards University assets. This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary. Core Qualifications + High school diploma or equivalent + Minimum 6 months of relevant experience + Preferred Certification CABT Knowledge, Skills and Attitudes: + Skill in completing assignments accurately and with attention to detail. + Ability to analyze, organize and prioritize work under pressure while meeting deadlines. + Ability to process and handle confidential information with discretion. + Ability to work evenings, nights, and weekends as necessary. + Commitment to the University’s core values. + Ability to work independently and/or in a collaborative environment. Any relevant education, certifications and/or work experience may be considered. The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more. UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for. The University of Miami is an Equal Opportunity Employer - Females/Minorities/Protected Veterans/Individuals with Disabilities are encouraged to apply. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here (https://www.hr.miami.edu/careers/eo-ada/index.html) for additional information. Job Status: Full time Employee Type: Temporary Pay Grade: H9

University of Miami

Biomedical Technician PER DIEM

Sirius Computer Solutions

FEED

OTHER

Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment. This is an excellent opportunity for entry level candidates pursuing a career in biomedical engineering, electronics, or healthcare technology to gain hands-on experience with critical medical devices.

Position Summary:We are seeking motivated and detail-oriented candidates to join our team as a Medical Device Technician. In this role, you will support the device team with maintenance, calibration, and functionality testing of medical equipment used in clinical or laboratory environments. This is an excellent opportunity for entry level candidates pursuing a career in biomedical engineering, electronics, or healthcare technology to gain hands-on experience with critical medical devices. Essential Duties and Responsibilities:<ul style="margin-top:0in;margin-bottom:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Assist in the inspection, testing, and preventive maintenance of a medical device such as inhalators.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Help with calibration procedures and performance verification under the supervision of certified technicians or engineers.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Document device maintenance, repairs, and compliance checks in accordance with regulatory standards (e.g., FDA, ISO 13485, Joint Commission).</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Support the setup and deployment of devices for clinical trials, simulations, or patient use.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Collaborate with biomedical engineers to ensure proper equipment functionality and safety.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Organize and track inventory of medical equipment, spare parts, and service records.</li></ul> Qualifications:<ul style="margin-top:0in;margin-bottom:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Currently pursuing a degree in Biomedical Engineering, Electrical Engineering, Healthcare Technology, or a related technical field.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Strong interest in medical technology, patient safety, and equipment maintenance.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Basic understanding of electronic components, mechanical systems, or instrumentation.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Ability to follow detailed instructions and standard operating procedures.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Strong attention to detail, communication, and teamwork skills.</li></ul> Preferred (but not required):<ul style="margin-top:0in;margin-bottom:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Previous coursework or hands-on experience with medical or lab equipment.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Familiarity with regulatory environments (e.g., FDA, CE, IEC 60601 standards).</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Basic knowledge of troubleshooting tools and multimeters.</li></ul> What You’ll Gain:<ul style="margin-top:0in;margin-bottom:0in"><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Hands-on experience with medical devices in a regulated healthcare or lab setting.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Insight into the workflow of biomedical technicians and clinical engineering teams.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Mentorship from professionals in the medical technology field.</li><li style="margin-top:0in;margin-right:0in;margin-bottom:8pt;line-height:115%;font-size:12pt;font-family:'aptos' , sans-serif">Enhanced understanding of healthcare standards, compliance, and safety protocols.\</li></ul> Why Join Us?We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands-on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.

Transpire BIO Inc.

Device Technician - Line Operator

Biomedical Engineering

Biomedicine

Biotech and Pharmaceutical

Business Growth

Calibration

Career Development

Clinical Laboratory

Clinical Trial

Detail Oriented

Electrical Components

Electrical Engineering

Electronic Engineering

Equipment Maintenance/Repair

FDA (Food and Drug Administration)

Functional Testing

Healthcare

ISO (International Organization for Standardization)

Identify Issues

Instrumentation

International Electro-Technical Commission (IEC)

Laboratory Equipment

Maintain Compliance

Maintenance Services

Medical Equipment

Mentoring

Patient Care

Patient Safety

Preventative Maintenance

Regulations

Regulatory Compliance

Safety Compliance

Standard Operating Procedures (SOP)

Standards of Care

Startup

Team Player

Testing

Trinet ATS Feed

We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors.

YEAR

Senior Manufacturing & Quality Engineer Title: Sr. Manufacturing & Quality Engineer Location: Miami, FL Industry: Medical Device -Engineering/Operations/Quality Schedule: Monday-Friday, 8am-5pm Employment Type: Direct hire Salary: Up to $130k with great benefits (health benefits 100% paid for) Company Overview: Join a dynamic and growing organization at the forefront of medical device manufacturing, where engineering excellence meets patient impact. In this highly visible role, you ll own both manufacturing and quality engineering initiatives playing a critical part in bringing innovative products to market while ensuring the highest standards of compliance and performance. Position Overview: As a Senior Manufacturing & Quality Engineer, you ll serve as a key technical leader across product development, manufacturing, and quality systems. You ll drive process optimization, lead validation efforts, and partner cross-functionally to ensure products are safe, effective, and scalable. Responsibilities: Product Development & Design Control<ul><li>Lead and support product development activities in compliance with design control requirements </li><li>Develop and execute Design Verification & Validation (DV&V) protocols </li><li>Review engineering drawings for tolerancing, manufacturability, and inspection readiness </li><li>Perform tolerance stack-ups and risk assessments to ensure robust designs </li><li>Author and maintain risk management documentation (dFMEA, pFMEA, uFMEA) </li><li>Support regulatory submissions with technical expertise and documentation </li></ul> Manufacturing Engineering & Process Excellence<ul><li>Design, develop, and optimize manufacturing processes using Lean, Six Sigma, and DFM principles </li><li>Lead continuous improvement initiatives to increase yield, reduce scrap, and improve throughput </li><li>Design and implement tooling, fixtures, and test equipment </li><li>Develop and maintain work instructions, assembly procedures, and BOMs </li><li>Troubleshoot production challenges and implement sustainable solutions </li><li>Lead process and equipment validations (IQ/OQ/PQ) </li></ul> Quality Engineering & Compliance<ul><li>Develop inspection methods, control plans, and statistical techniques (MSA, validation methods) </li><li>Lead investigations (nonconformances, CAPAs, deviations, complaints) using root cause analysis, technical writing </li><li>Ensure compliance with FDA QMSR, ISO 13485, and ISO 14971 </li><li>Support internal/external audits and regulatory inspections </li><li>Develop and validate test methods and inspection tooling </li></ul> Leadership & Cross-Functional Collaboration<ul><li>Act as a technical bridge across Engineering, Quality, Operations, and Supply Chain </li><li>Partner with suppliers to improve quality and support qualification efforts </li><li>Mentor junior engineers and inspectors, fostering a high-performance culture </li><li>Champion continuous improvement, accountability, and quality excellence </li></ul> Documentation & Systems<ul><li>Maintain engineering documentation in systems such as EPDM and Greenlight Guru </li><li>Generate validation protocols, technical reports, and test documentation </li><li>Ensure strong document control and traceability </li></ul> Qualifications<ul><li>Bachelor s degree in Mechanical, Biomedical, or related Engineering field </li><li>8+ years of experience in manufacturing and/or quality engineering within class I and/or II medical device </li><li>Proficiency in CAD (SolidWorks preferred) </li><li>Strong communication and problem-solving skills </li><li>Bi-lingual, English and Spanish language skills </li><li>Independent, self-starter and capable of solving problems</li><li>Strong expertise in: <ul><li>Design controls & product development </li><li>Process validation (IQ/OQ/PQ) </li><li>CAPA, root cause analysis, and quality systems </li><li>Inspection methods, metrology, and MSA </li><li>Lean Manufacturing and/or Six Sigma </li></ul></li></ul> Why Join?<ul><li>High-impact role with visibility across the organization </li><li>Opportunity to influence both product development and manufacturing strategy </li><li>Collaborative, cross-functional environment </li><li>Strong growth potential within a regulated, innovation-driven industry </li><li>Competitive compensation and benefits </li></ul> EOE/ADA IND123 SRG4 Life Sciences delivers flexible staffing solutions nationwide, specializing in pharmaceutical, CDMO/CMO, medical device, clinical research, PBM, pharmacy, food and beverage, nutraceutical, laboratory, and consumer product sectors. We provide contract, contract-to-hire, and direct hire placements across a wide range of critical roles including Scientists, Formulators, Engineers, QA/Regulatory Affairs, Microbiologists, Manufacturing Technicians, Supply Chain/Procurement Specialists, Project Managers, and Business Development professionals. SRG4 Life Sciences operates on a relationship-driven model partnering closely with clients to understand not only the role, but the company s culture, goals, and vision. Our mission is to match purpose-driven professionals with organizations committed to advancing human health, building long-term partnerships that drive innovation, quality, and performance.

The Staffing Resource Group, Inc

Sr. Manufacturing and Quality Engineer

Bill of Materials (BOM)

Biology

Bridge Building

Business Development

CAD/CAM (Computer-Aided Design/Computer-Aided Manufacturing)

Civil Engineering

Clinical Research

Communication Skills

Compensation and Benefits

Consulting

Continuous Improvement

Corrective and Preventative Action (CAPA) Systems

Cross-Functional

Design Failure Mode and Effects Analysis (DFMEA)

Design Verification

Documentation

Engineering Drawing

English Language

External Audit

Food and Beverage Industry

Human Health

Internal Audit

Leadership

Lean Manufacturing

Lean Six Sigma

Machine Tool

Manufacturing

Manufacturing Engineering

Manufacturing Systems

Manufacturing/Industrial Processes

Metrology

Multilingual

Pharmacy

Problem Solving Skills

Process Failure Mode and Effects Analysis (PFMEA)

Process Improvement

Process Validation

Product Design

Product Development

Product Support

Productivity Management

Project/Program Management

Purchasing/Procurement

Quality Assurance

Quality Assurance Methodology

Quality Engineering

Quality Management

Regulatory Submissions

Risk Analysis

Risk Management

Root Cause Analysis

SolidWorks

Spanish Language

Supply Chain

Supply Chain Operations

Technical Leadership

Technical Writing

Test Equipment

Test Fixtures

Test Plan/Schedule

Validation Plan

Validation Testing

Writing Skills

HaleyMarketing

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Biomedical Equipment Technician Jobs in Miami, FL

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Biomedical Technician PER DIEMUniversity of Miami

Device Technician - Line OperatorTranspire BIO Inc.

Sr. Manufacturing and Quality EngineerThe Staffing Resource Group, Inc

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