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<h3>Job Description</h3>
Job Description
Position Summary:
We are seeking a detail-oriented and hands-on Secondary Operations Engineer / Process Engineer to join our medical tubing manufacturing team. This role is responsible for the development, validation, and continuous improvement of secondary operations processes to ensure high-quality, cost-effective production of medical-grade tubing products. The ideal candidate will bring strong technical skills, process engineering experience, and a deep understanding of quality standards within a regulated manufacturing environment.
Key Responsibilities:
<ul>
<li>Develop, implement, and optimize secondary operations for medical tubing, including cutting, hole punching, tipping, flaring, bonding, printing, molding and assembly.</li>
<li>Design and validate fixtures, tools, and equipment to support post-extrusion processes.</li>
<li>Collaborate with suppliers and equipment vendors for tooling design, maintenance, and upgrades.</li>
<li>Create, implement and maintain process documentation (work instructions, process flows, validation protocols, etc.).</li>
<li>Work with cross-functional teams (R&amp;D, Quality, Production) to support new product introductions and process scale-up.</li>
<li>Collaborate with Sales on evaluating and quoting new products, new product development and customer support. Participate in weekly review meetings to align capabilities with customer specifications.</li>
<li>Work with quality to conduct root cause analysis and lead corrective/preventive actions (CAPA) for process issues or non-conformances.</li>
<li>Train and support operators on new or revised secondary processes.</li>
<li>Follow and maintain a schedule of active projects and give necessary updates.</li>
<li>Drive continuous improvement and cost reduction initiatives using lean manufacturing and Six Sigma principles.</li>
<li>Facilitate project scale up activities including transferring manufacturing across multiple locations.</li>
</ul>
Qualifications:
<ul>
<li>Bachelor’s degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or related field.</li>
<li>5+ years of experience in medical device manufacturing or plastic tubing industry.</li>
<li>Hands-on experience with secondary operations processes and automation.</li>
<li>Familiarity with GMP, ISO 13485, and FDA regulations.</li>
<li>Strong troubleshooting skills and knowledge of statistical process control.</li>
<li>Experience with validation (IQ/OQ/PQ) and process documentation.</li>
<li>Excellent communication, documentation and project management skills.</li>
</ul>
Preferred Skills:
<ul>
<li>Experience with laser cutting, RF welding, or thermal bonding.</li>
<li>Proficient in CAD software (SolidWorks or similar) and Microsoft Office Suite.</li>
<li>Knowledge of polymer materials commonly used in medical devices (e.g., PVC, Pebax, Polyurethane).</li>
<li>Lean Six Sigma certification (Green Belt or higher).</li>
<li>Bilingual in Spanish, a plus</li>
<li>Prior Secondary Operations experience on molded or manufactured parts</li>
</ul>
Proterial Cable America, Inc. is a second chance employer. We believe in giving individuals who have made past mistakes an opportunity to rebuild their lives and contribute positively to society. People with criminal records are encouraged to apply.

Secondary Ops Engineer / Process Engineer

<h3>Job Description</h3>
Job DescriptionEssential Functions:
<ul>
<li>Creates preliminary layouts, sketches, and notes to be used during product design process.</li>
<li>Checks completed layouts and drawings for clarity, completeness, and conformity to Company standards.</li>
<li>Develops and designs products and assemblies using CAD software and drafting tools.</li>
<li>Investigates and develops solutions to problems of limited scope and complexity; drafts reports detailing investigations, problems, and solutions.</li>
<li>Assists in maintaining reliability compliance processes and procedures to meet regulatory requirements.</li>
<li>Works with other engineers to create and implement production operating procedures.</li>
<li>Reviews product specifications and determines design requirements and scope of work.</li>
<li>Generates design concepts in conformance with product specifications and established engineering principles.</li>
<li>Provides technical and mechanical support to production departments for established processes.</li>
<li>Supports the risk management activities for medical devices.</li>
<li>Assists in some phases of product development as directed.</li>
<li>Assists in the analysis of designs.</li>
<li>Assists in process and/or equipment troubleshooting</li>
<li>Conducts tests utilizing established test protocols.</li>
</ul>
Minimum Qualifications:
<ul>
<li>Bachelor of Science degree in Mechanical or Biomedical Engineering, or any equivalent education and/or experience from which comparable knowledge, skills and abilities have been demonstrated/achieved. Advanced degree is preferred.</li>
<li>Minimum six (6) months of experience in an Engineering position or internship preferred.</li>
<li>Class II medical device R&amp;D experience preferred.</li>
<li>CAD experience using SolidWorks or equivalent</li>
</ul>
Pay range: $29.80 to $34.00/hr
Exact compensation may vary based on skills and experience.

Design Engineer

<h3>Job Description</h3>
Job Description
Job Summary
The Product Development Engineer will be responsible for supporting the research, design, and development of implants and instrumentation using primarily metal and polymer 3D printing. The position will include work along the entire product development lifecycle through launch to market including initial design and development, testing, regulatory submissions, quality system documentation, and field support.
Duties and responsibilities
<ul>
<li>Supporting the design and engineering efforts for company products, which may include, but is not limited to:</li>
<ul>
<li>Developing clinical use understanding of restor3d &amp; market research through literature and interactions with internal team &amp; surgeon design teams</li>
<li>Researching current surgical techniques and design considerations</li>
<li>Modeling implant, instrument (drivers, depth gauges, drill guides, etc.), and fixture 3D CAD models/drawings using modeling software (SolidWorks)</li>
<li>Printing metal and polymer prototypes </li>
<li>Identifying feasibility and verification testing requirements and conducting testing</li>
<li>Documenting the design process in accordance with company quality procedures including development plans, design inputs &amp; outputs, drawings, labeling, risk documentation, verification &amp; validation plans/reports, and regulatory submission items</li>
</ul>
<li>Collaborating with operations, manufacturing engineers, and suppliers to support new product development and sustaining efforts</li>
<li>Developing and managing project timelines for line extensions and sustaining engineering efforts</li>
</ul>
<ul>
<li>Working with the commercial team to support launch strategy and forecasting</li>
<li>Performs other related duties as assigned</li>
</ul>
Qualifications and experience
Required Skills: 
· Excellent verbal and written communication skills
· Excellent organizational skills, with the ability to prioritize work.
Education and Experience:
<ul>
<li>Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or equivalent Engineering</li>
<li>Experience with 3D modeling software (Solidworks, ProE, 3-matic, Fusion360, Rhino, etc.)</li>
<li>Ability to read and understand scholarly journal articles</li>
<li>Independent worker willing to learn and develop necessary design, manufacturing, and software skills though guided trainings and self-guided research</li>
<li>Self-starter willing to take ownership of assigned projects and action items</li>
</ul>
Preferred education and experience:
<ul>
<li>Previous experience within medical device industry strongly preferred</li>
<li>Knowledge of human anatomy (through coursework or training)</li>
<li>Understanding of working under a quality management system for medical devices</li>
<li>Demonstrated ability of working with design control activities and verification &amp; validation activities in medical device development (ISO 13485 and FDA 21 CFR 820)</li>
<li>Familiarity with orthopedic implant field</li>
<li>Experience with basic hand tools, 3D printers, materials testing frames, cleaning and inspection equipment</li>
<li>CSWA certification</li>
<li>Ability to work flexible hours, if necessary</li>
</ul>
Physical Requirements: 
· Prolonged periods sitting at a desk and working on a computer.
· Must be able to lift up to 15 pounds at times.

Product Development Engineer

<h3>Job Description</h3>
Job DescriptionDescription:
RIVANNA is seeking a Product Development Engineer to join our dynamic engineering team. You will work with a talented team of professionals as we strive to achieve our mission to develop and commercialize world-first imaging-based medical technologies that elevate global standards of care. As a Product Development Engineer, you will contribute to activities across the product lifecycle, from prototype development to clinical support. This hands-on multidisciplinary role involves close collaboration with the mechanical, manufacturing, and electrical engineering team on a wide range of product development tasks and projects. This job will be on-site in Charlottesville, VA; applicants must be local or willing to relocate to Charlottesville for this position.
 
Responsibilities
<ul>
<li>Product Development: Support the development and improvement of medical devices and manufacturing processes </li>
<li>Testing: Design and execute test methods to verify subsystem and system performance, analyze data, and document results in test reports</li>
<li>Prototyping &amp; Fabrication: Operate and maintain 3D printers and machine shop equipment (e.g., mill, lathe, drill press) to support prototype and fixture fabrication</li>
<li>Manufacturing: Assist with the assembly of electromechanical systems for engineering builds, internal testing, and clinical evaluation</li>
<li>Documentation: Create and update design control and design transfer documentation including work instructions, BOMs, test plans, and test reports</li>
<li>Field Service: Provide technical support for systems in the field, including remote troubleshooting and occasional travel to clinical sites</li>
<li>Cross-functional Collaboration: Work closely with engineering, production, and clinical teams to support product development and sustaining efforts</li>
</ul>
Requirements:
<ul>
<li>Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related engineering discipline</li>
<li>1-3 years of relevant industry experience in product development or R&amp;D (medical device experience preferred)</li>
<li>Hands-on experience with hand tools, power tools, 3D printing, soldering, and test equipment</li>
<li>Experience with SolidWorks or similar CAD software preferred</li>
<li>Exposure to medical device regulations and quality systems including ISO 13485, FDA design controls (21 CFR), and risk management processes (ISO 14971).</li>
<li>Strong organizational, communication, and technical writing skills</li>
<li>Ability to work independently and on cross-functional teams in a fast-paced environment</li>
<li>Willingness to travel occasionally (=10%) for field service support</li>
<li>Applicants must be authorized to work in the United States without the need for current or future sponsorship. RIVANNA is unable to provide employment sponsorship for this position.</li>
</ul>
About Rivanna Medical, Inc.: RIVANNA® is a privately held designer, manufacturer, and distributor of world-first, imaging-based medical solutions based in Charlottesville, VA. RIVANNA operates an FDA-registered and ISO 13485:2016 certified manufacturing facility where it produces the Accuro® product line and related medical equipment and components. Accuro is the world's first spinal navigation device designed to improve the safety, speed, and efficiency of spinal needle guidance procedures. RIVANNA's revolutionary platforms feature BoneEnhance® Multi-Frequency Image Reconstruction, which optimizes ultrasound for the visualization of bony versus soft tissue anatomy, and SpineNav3D™ AI-Based Spine Recognition, which automates ultrasound image interpretation.
 
Employee Benefits at Rivanna Medical: Rivanna Medical offers a comprehensive benefits package, which includes health insurance, vision and dental coverage, group life insurance, long-term disability insurance, paid time off, a 401(k) plan with company match, and more. We are continually seeking to enhance our team with individuals who bring unique perspectives and experiences. This diversity of thought and perspective drives innovation and strengthens our commitment to creating an inclusive team environment where our core values of trust, humility, and dedication are practiced every day.
 
Equal Employment Opportunity Statement: Rivanna Medical is committed to providing equal employment opportunities to all employees and applicants without regard to race, ethnicity, religion, color, sex (including childbirth, breastfeeding, and related medical conditions), gender, gender identity or expression, sexual orientation, national origin, ancestry, citizenship status, uniform service member and veteran status, marital status, pregnancy, age, protected medical condition, genetic information, disability, or any other protected status in accordance with all applicable federal, state, and local laws.All employees must be able to lift at least 25 pounds. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of their positions.

<h3>Job Description</h3>
Job Description
IEC 62304 Quality Specialist (Design Assurance Engineer)
No C2C. Fulltime permanent role (no sponsorship). Note: non-medical device industry exp application will NOT be considered.
Overview
We are looking a highly skilled IEC 62304 expert as Software Quality Engineer to work in Austin, TX (Onsite).
MUST Have: hands-on experience with
<ul>
<li>IEC 62304 (Medical Device Software Life Cycle Processes)</li>
<li>ISO 14971 (Risk Management for Medical Devices)</li>
<li>ISO 13485 (Quality Management Systems)</li>
<li>FDA 21 CFR Part 820 (Quality System Regulation)</li>
</ul>
This role will ensure the highest standards of medical devices software quality, safety, cybersecurity and compliance for medical device products. In this role, you will collaborate closely with cross-functional teams to support the full software development lifecycle, from design and risk management to verification, validation, and regulatory submission. You will apply your expertise in regulatory standards, software quality processes, and system-level thinking to ensure that our products meet both user needs and global regulatory requirements.
Key Responsibilities
<ul>
<li>Ensure full compliance with global medical device regulations and standards, including:</li>
</ul>
1. IEC 62304 (Medical Device Software Life Cycle Processes)
2. ISO 14971 (Risk Management for Medical Devices)
3. ISO 13485 (Quality Management Systems)
4. FDA 21 CFR Part 820 (Quality System Regulation)
5. 21 CFR Part 11 (Electronic Records and Signatures)
6. Cybersecurity guidance for medical devices (e.g., FDA premarket guidance, AAMI TIR57/97, etc.)
<ul>
<li>Review, maintain, and improve Quality System procedures and work instructions governing software development, validation, and lifecycle management for embedded, standalone, and cloud-based medical device software.</li>
<li>Partner closely with cross-functional teams including R&amp;D, Systems Engineering, Regulatory Affairs, Manufacturing, and Clinical teams to ensure that software development activities are fully integrated with design controls and compliant with applicable standards.</li>
<li>Review and approve software design documentation, including:</li>
</ul>
1. Software Development Plans
2. Software Requirements Specifications (SRS)
3. Software Architecture and Design Documents
4. Risk Management documentation (including Software Failure Modes and Effects Analysis)
5. Verification and Validation protocols, test plans, test cases, and reports.
<ul>
<li>Conduct software quality audits and assessments to ensure compliance with internal processes, SOPs, and applicable regulatory requirements.</li>
<li>Actively participate in software risk management processes, facilitating hazard analyses, failure mode assessments, and risk mitigations throughout the product lifecycle.</li>
<li>Provide oversight and review of process validation protocols for software systems used in manufacturing, testing, installation, service, and support of medical devices.</li>
<li>Support regulatory submissions including 510(k), PMA, CE Technical Files, and international regulatory dossiers, ensuring complete and compliant software documentation.</li>
<li>Participate in usability testing, clinical lab evaluations, cadaveric labs, and design validation activities to ensure software meets intended use and user needs.</li>
<li>Provide expert guidance to teams during internal and external audits (e.g., FDA inspections, Notified Body audits, MDSAP audits).</li>
<li>Assist in design transfer activities to ensure smooth transition from product development to manufacturing with appropriate validation of test methods, process controls, and inspection methods.</li>
<li>Provide statistical analysis and support for software defect trending, CAPA investigations, and continuous improvement activities.</li>
</ul>
Qualifications
<ul>
<li>Bachelor’s degree in Software Engineering, Computer Science, Biomedical Engineering, Electrical Engineering, or related technical discipline. Master’s degree preferred.</li>
<li>Minimum 5+ years of hands-on experience as a Software Quality Engineer in the medical device industry (Class II and/or Class III devices preferred).</li>
<li>In-depth knowledge of design controls, risk management, and software lifecycle processes specific to regulated medical devices.</li>
<li>Demonstrated experience with IEC 62304-compliant software development and verification/validation processes.</li>
<li>Strong working knowledge of ISO 14971, ISO 13485, 21 CFR Part 820, and current FDA guidance documents related to software in medical devices.</li>
<li>Prior experience supporting 510(k), PMA, EU MDR, or other international regulatory submissions for medical device software.</li>
<li>Ability to collaborate effectively with cross-functional teams and communicate quality requirements clearly to both technical and non-technical stakeholders.</li>
<li>Excellent written, verbal, and interpersonal communication skills.</li>
<li>Certified Software Quality Engineer (CSQE), ASQ, RAC, or other relevant certifications are a plus.</li>
</ul>
Preferred Experience (Nice to Have)
<ul>
<li>Experience with connected medical devices, or software as a medical device (SaMD).</li>
<li>Familiarity with cybersecurity frameworks applicable to medical device software.</li>
<li>Experience with cloud-based or mobile medical applications.</li>
<li>Direct interaction with FDA, Notified Bodies, or MDSAP auditors during inspections.</li>
</ul>

IEC 62304 Expert (Design Assurance Engineer)

<h3>Job Description</h3>
Job Description
Job Description:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Reporting to Chief Technical Officer
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Looking for a creative developer excited by the prospect of bringing novel biotechnology to market in a fast-paced start-up environment.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; The successful candidate will lead the mechanical development team of the Proteowise instrument and the disposable fluidic devices that go with it.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Responsibility extends from breadboards and prototypes through close involvement with the manufacturing teams who will implement the candidate’s designs into commercial products.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Must be hands-on with prototypes and evaluate their designs in the lab.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Will work closely with the internal cross-functional development team of Software Engineers, Electrical Engineers, Optical Engineers, Biologists and Chemists to ensure systems are successfully implemented.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Will work closely with the Manufacturing and Quality teams to transfer manufacturable designs.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Will work closely with the Industrial design partner to faithfully implement the Proteowise vision.
Skill &amp; Experience Requirements:
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Must be fluent in the design and debugging methods of mechanical systems, and capable of producing mechanical parts and subsystems in house and using 3rd party suppliers.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Must be expert in Solidworks.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Experience with fluidic analyses and simulations a plus.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Successful track record of commercial launch, especially launching fluidic, microfluid disposables a plus
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; BS Mechanical or BS Biomedical Engineer. MS or PhD a plus.
·&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; 5 years industry experience. More a plus.

Lead Mechanical Engineer

<h3>Job Description</h3>
Job Description
Overview
Now Hiring Field Service Engineer Ultrasound!Location: Washington, DC*Some regional travel may be required*Salary: Starting at $60,000 annually based on experience. Who We Are:
Tri-Imaging Solutions is at the forefront of medical imaging equipment innovation, specializing in enterprise imaging systems management. We’re committed to delivering cutting-edge solutions and empowering our team with the tools, training, and opportunities to grow. Join our dynamic team and play a vital role in advancing healthcare technology.
Why Join Us (Benefits):
<ul>
<li>
Highly competitive salary
</li>
<li>
Car/travel reimbursement
</li>
<li>
Continuing diagnostic imaging training (with a path into advanced modalities like CT, MRI, and Cath Lab)
</li>
<li>
Company-paid holidays plus PTO
</li>
<li>
Major medical/dental/vision benefits
</li>
<li>
Recognition/reward program
</li>
</ul>
Position Overview:
We are seeking a motivated Level 1 Field Service Engineer with a primary focus on ultrasound systems. This is an excellent opportunity for early-career professionals with a strong technical foundation who want to expand into other diagnostic imaging modalities over time. The right candidate will receive structured training and mentorship to build expertise across the full spectrum of imaging technology.
What You’ll Do:
<ul>
<li>
Perform installations, calibrations, inspections, and basic repairs on general ultrasound equipment
</li>
<li>
Conduct preventive maintenance in accordance with OEM specifications
</li>
<li>
Use laptop-based diagnostic tools and hand tools to assess and improve system performance
</li>
<li>
Collaborate closely with senior engineers to develop advanced troubleshooting skills
</li>
<li>
Provide excellent customer service while ensuring equipment operates to the highest safety and performance standards
</li>
<li>
Travel to client sites within the assigned territory
</li>
</ul>
What You’ll Need (Requirements):
<ul>
<li>
Associate degree in Biomedical Engineering, Electrical Engineering, or related field, or equivalent work experience
</li>
<li>
1–2 years of hands-on experience as a biomedical or ultrasound service technician
</li>
<li>
Strong mechanical aptitude and diagnostic skills
</li>
<li>
Eagerness to learn other imaging modalities such as CT, MRI, and Cath Lab
</li>
<li>
Excellent communication and teamwork abilities
</li>
<li>
Willingness to travel regionally as needed
</li>
</ul>

Field Service Engineer Ultrasound

<h3>Job Description</h3>
Job Description
Are you a mechanical maestro ready to unleash your expertise? At BDC Laboratories, we invite you to immerse yourself in an exhilarating role as a Full-Time Product Evaluations Engineer III onsite in Wheat Ridge, CO. This isn’t just any gig; it’s an opportunity to innovate and solve real-world problems, all while collaborating with a vibrant team that values customer satisfaction above all.
As you dive into engaging projects that drive the biotech industry forward, you'll enjoy a competitive salary ranging from $95,000 to $112,000. Here, your ingenuity and keen eye for excellence will be recognized, not just encouraged. The thrill of working in a dynamic, energetic environment awaits you!
You will be provided great benefits such as Medical, Dental, Vision, 401(k), Health Savings Account, and Paid Time Off. Don’t miss the chance to be at the forefront of biotechnology, where every day is a new adventure. Elevate your career with us today!
Let us introduce ourselves
Biomedical Device Consultants &amp; Laboratories (<a href="http://www.bdclabs.com" target="_blank">www.bdclabs.com</a>) is a fast-growing company that offers comprehensive medical device testing services, designs verification test equipment, and produces silicone mock vessels to the medical device community in support of domestic and international regulatory submissions and approvals. Our primary focus is cardiovascular technologies such as endovascular stents, prosthetic heart valves, and catheters. As a small company, BDC's environment is fast-paced, dynamic, challenging, and rewarding.
Your day to day as a Product Evaluations Engineer III
As a Full-Time Product Evaluations Engineer III at BDC Laboratories, your mission is to ensure that every piece of equipment meets the rigorous demands of our biotech studies. You’ll assess the suitability of equipment for data acquisition, ensuring compliance with protocol specifications. Your expertise will keep our laboratory inspection-ready, as you guarantee all equipment is designed for optimal performance, adequately cleaned, and meticulously maintained. You'll lead the way in establishing innovative test methods, preparing meticulous protocols, and maintaining a contamination-free environment.
Each data entry you record will enhance the integrity of our research, as you diligently verify and analyze experimental data. Additionally, you will play a key role in supporting our Quality Management System and participating in audits, all while setting an exemplary standard for your colleagues. This position is not just about maintaining excellence; it's about driving innovation in a fun, high-performance culture.
Requirements for this Product Evaluations Engineer III job
To thrive as a Full-Time Product Evaluations Engineer III at BDC Laboratories, you’ll need a robust toolkit of skills and experiences. A minimum of a Bachelor’s Degree in engineering or a science-based field, coupled with relevant years of experience, establishes your foundational expertise. Familiarity with quality system requirements like ISO 17025 and 21 CFR Part 58 is preferred, while knowledge of ISO 13485 and 21 CFR Part 820 will set you apart. Your analytical and problem-solving prowess will be crucial, allowing you to perform statistical analyses and interpret technical regulations effectively. Strong verbal and written communication skills are essential for drafting clear protocols and presenting information to both managers and team members.
Additionally, your ability to mentor and manage fellow engineers will contribute to a dynamic and collaborative team environment. Embrace this opportunity to lead with integrity in a forward-thinking biotech space!
Knowledge and skills required for the position are: 
<ul>
<li>Minimum of a Bachelor’s Degree in an engineering field and 4 years of experience; or minimum of a Master’s Degree in an engineering field and 2 years of experience; or minimum of a Bachelor’s Degree in a science-based field and 6 years of relevant experience; or an Associate Degree with a minimum of 10 years of relevant experience.</li>
<li>Understanding of quality system requirements including ISO 17025 and 21 CFR part 58 is preferred. Experience in 21 CFR Part 820 and Part 11, ISO 13485 and other relevant international standards desirable.</li>
<li>Must be organized with excellent analytical and problem-solving abilities and the ability to perform and report basic statistical analyses.</li>
<li>Ability to read analyze and interpret technical procedures and governmental regulations; along with the ability to effectively present information and respond to questions from managers and team members. Ability to effectively draft protocols and reports.</li>
<li>Ability to define problems, collect data, establish facts and draw valid final conclusions.</li>
<li>Strong verbal and writing skills and good interpersonal and leadership skills.</li>
<li>Proficiency with a Windows environment(Word and Excel) required.</li>
<li>Experience managing other engineers.</li>
</ul>
Get started with our team!
If you feel that this job is what you're looking for, applying is a piece of cake - just follow the instructions on this page. Good luck!
 Job Posted by ApplicantPro

Product Evaluations Engineer III

<h3>Job Description</h3>
Job DescriptionSalary: 
Position Description
The Clinical Engineer is a skilled data-savvy contributor who receives and organizes inbound clinical data in various formats from multiple research sites engaged in Carlsmed-sponsored studies. The role involves receiving, vetting, and forwarding medical images to measurement services and parsing large data sets into subsets for analysis.
 
Key Responsibilities
<ul>
<li>Receiving and preparing incoming data from multiple clinical studies</li>
<li>Sorting and organizing information in various formats, including numerical values, categorical attributes, medical imaging, patient surveys, and free-text medical notes</li>
<li>Organizing and forwarding medical images to measurement services</li>
<li>Collating and formatting data for statistical analysis</li>
<li>Creating tables, charts, and figures for internal and external reports.</li>
<li>Preparing PowerPoint presentations and manuscript materials</li>
</ul>
 
Skills
<ul>
<li>Data organization: tabulating, sorting, and analyzing scientific data</li>
<li>Advanced user of MS-Office software (Word, Excel, PowerPoint)</li>
<li>Desired: Proficient with Python for data cleaning and formatting</li>
<li>Effective communication and presentation skills.</li>
</ul>
<ul>
<li>Continuous issue detection and resolution.</li>
</ul>
 
Qualifications
<ul>
<li>BS degree in a technical field such as Engineering, Life Sciences, Computer Sciences, Mathematics or related medical/scientific field. MS degree preferred.</li>
<li>Experience with digital image software, preferably medical imaging software</li>
<li>Highly desired: previous contributions to biomedical or biological studies</li>
<li>Highly desired: knowledge/experience in spine/orthopedics</li>
</ul>
Equal Opportunity Employer
Carlsmed is an equal-opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Carlsmed is committed to providing reasonable accommodation for candidates with disabilities in our recruitment process. If you need any assistance or accommodation due to a disability, please let us know.
 
Compensation
We are pleased to provide a competitive salary and benefits. Our benefits reflect our investment in the overall health and well-being of our employees and their families. including paying 100% of monthly healthcare, dental and vision insurance premiums, a 401(k) plan with employer matching, and unlimited PTO. The expected pay range for this position is $95,000 - $120,000. Compensation may vary based on related skills, experience, and relevant key attributes.

Clinical Engineer

<h3>Job Description</h3>
Job DescriptionDescription:
Title: Clinical Engineer Manager
Department: Service
Reports to: President
Location: Onsite Montgomery, AL
 
Radon Medical Imaging is a world-class distributor of industry leading radiology equipment, a trusted independent medical device service provider specializing in multi-vendor service and asset management, and a leader in refurbishing high-end radiology equipment. We pride ourselves on delivering exceptional service, innovative solutions, and operational excellence to our partners and clients. Radon is a Private Equity backed company on an aggressive growth trajectory with several completed acquisitions creating exciting opportunities for innovation, scalability, and career advancement.
 
Job Summary:
The BMET Team Lead is responsible for supervising and guiding biomedical technicians, ensuring high-quality service delivery in the maintenance, repair, and calibration of clinical equipment. This role involves hands-on technical work, training, administrative support, and coordination with internal teams and external vendors to maintain compliance and safety standards. Communication with administrators, nurses, managers in a professional manner to satisfy their needs and to grow relationships into more business is crucial.
 
Responsibilities:
· Leads and supervises biomedical technicians, ensuring high-quality work and providing cross-training in equipment testing, calibration, operation, and troubleshooting.
· Coordinates with supervisory personnel on equipment status and promptly reports any patient or operatory safety concerns.
· Performs inspections, repairs, installations, and calibrations of clinical equipment in compliance with current policies and procedures, including planned maintenance and electrical safety checks.
· Assists in the evaluation and selection of new equipment, accessories, and supplies to support clinical operations.
· Supports administrative functions such as managing work orders, maintenance records, PM schedules, and inventory, while maintaining accurate documentation.
· Utilizes office automation tools and diagnostic software appropriate to the equipment and contributes to service delivery improvements.
· Oversees services provided by external vendors, ensuring quality control, and managing the ordering of parts and maintenance of technical literature.
· Inspects incoming equipment for compliance with applicable codes and standards and assists in maintaining calibration programs for testing equipment.
· Maintains up-to-date knowledge of regulatory requirements and ensures adherence to relevant codes, standards and policies.
· Completes tasks efficiently with minimal supervision and demonstrates strong initiative in planning, time management, and cost control.
· Attend and participate in Environment of Care (EOC) meetings. Prepare and present safety committee reports.
Requirements:
Qualifications:
<ul>
<li>High School diploma or equivalent</li>
<li>5+ years experience in BMET role or similar</li>
<li>2+ years leadership experience</li>
<li>Experience working with patient monitoring equipment</li>
<li>Multiple modalities preferred</li>
<li>Ability to lift and/or move objects of 50lb consistently</li>
<li>Regularly stand, walk, stoop, kneel, crouch, or crawl</li>
<li>Self-motivated, eager, and driven individual willing to learn new modalities</li>
<li>Dependable and reliable</li>
</ul>
Schedule: 8-hour shift
Full time role, onsite at Jackson Hospital
If you have the skills and experience to excel in this role, we invite you to apply and join our team dedicated to delivering cutting-edge medical imaging solutions.
Why Work With Us:
<ul>
<li>Growing company</li>
<li>401k with company match</li>
<li>Medical benefit package</li>
<li>Company covered dental</li>
<li>100% company paid Long Term Disability</li>
<li>$250,000 Life Insurance policy</li>
<li>10 holidays</li>
<li>PTO and sick days</li>
<li>Paid Training</li>
</ul>

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