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<h3>Job Description</h3>
Job Description
BioView is seeking a highly professional customer focused Field Service Engineer to join our Support &amp; Training team. The successful candidate will live in the Boston, MA area and serve as a support and training engineer for our clients in the Americas. He/She will provide our new and existing customers comprehensive training of the BioView imaging products line. He/She will be responsible for providing prompt support to our users, while achieving the highest possible level of customer satisfaction. He/She will maintain a high level of technical expertise in all aspects of the BioView products, including the biological, computerized and optical features of our products.
Essential Duties and Responsibilities
· Installation of BioView systems at customers sites
· Training of new users to successfully operate the BioView systems &amp; software
· Demonstrating BioView systems and applications
· Provide remote and on-site support to BioView customers by installing, fine-tuning, and maintaining BioView systems and applications.
<ul>
<li>The position requires diagnosing and resolving mechanical, hardware, software, and system failures</li>
<li>You will document all activities, contribute to quality improvement, and focus on maximizing customer satisfaction</li>
<li>Frequent travel required, 60-70% of the time, mostly within the US &amp; Canada, but may be to other regions on the globe</li>
</ul>
Requirements
<ul>
<li>Bachelor’s degree or equivalent in life science, biomed, or a technical field</li>
<li>Familiarity with Microscopy, Cytogenetics, Fluorescence In-situ Hybridization (FISH), Cell Morphology, and Immunostaining analysis is an advantage.</li>
<li>Excellent communication (verbal and written) and interpersonal skills.</li>
<li>Problem solver with good technical aptitude and troubleshooting skills</li>
<li>Computer and network knowledge is a plus</li>
<li>Ability to understand computer algorithms and to tune parameters.</li>
<li>Outstanding ability to explain, demonstrate and present new biological and technical concepts to new users</li>
</ul>
Other requirements
<ul>
<li>Handle stress effectively</li>
<li>Willingness to work outside of normal working hours and in rare cases on weekends</li>
<li>Valid Passport</li>
<li>Valid driver license</li>
</ul>
Company DescriptionOur Mission is to improve cancer patient’s assessments and outcomes. BioView develops, manufactures, and markets innovative Automated cell imaging and analysis platforms for use in cytology, cytogenetics and pathology at clinical and research laboratories who wish to digitize and streamline their analysis workflow. BioView’s industry-leading platforms offer advanced capabilities for Fluorescent and Bright-field based applications driven by Artificial intelligence. Starting from automated FISH Analysis of tissue and cells suspension for cancer and genetic abnormalities, to automated whole slide imaging for digital pathology and quantitative IHC scoring application for nuclear &amp; membrane staining. Bringing liquid Biopsy to the clinical Practice We are a world leader in providing solutions for Circulating tumor cells detection, enumeration and characterization. Our all-in-one DeNovo system, offers high levels of speed, standardization and sensitivity. It is easy to operate, and can be integrated with any CTC enrichment method, as well as any combination of immunofluorescence and FISH markers. NGK – New Generation Karyotyping An innovative platform powered by deep learning dramatically enhances technician efficiency and productivity and introduces first of a kind supervisor monitoring tools and an ISCN results generator that is directly linked to an online supporting cytogenetics database. Our customers leverage offline analysis and Web-based applications to collaborate with their colleagues and explore new business opportunities. 
<h3>Company Description</h3>
Our Mission is to improve cancer patient’s assessments and outcomes. BioView develops, manufactures, and markets innovative Automated cell imaging and analysis platforms for use in cytology, cytogenetics and pathology at clinical and research laboratories who wish to digitize and streamline their analysis workflow. BioView’s industry-leading platforms offer advanced capabilities for Fluorescent and Bright-field based applications driven by Artificial intelligence. Starting from automated FISH Analysis of tissue and cells suspension for cancer and genetic abnormalities, to automated whole slide imaging for digital pathology and quantitative IHC scoring application for nuclear &amp; membrane staining. Bringing liquid Biopsy to the clinical Practice We are a world leader in providing solutions for Circulating tumor cells detection, enumeration and characterization. Our all-in-one DeNovo system, offers high levels of speed, standardization and sensitivity. It is easy to operate, and can be integrated with any CTC enrichment method, as well as any combination of immunofluorescence and FISH markers. NGK – New Generation Karyotyping An innovative platform powered by deep learning dramatically enhances technician efficiency and productivity and introduces first of a kind supervisor monitoring tools and an ISCN results generator that is directly linked to an online supporting cytogenetics database. Our customers leverage offline analysis and Web-based applications to collaborate with their colleagues and explore new business opportunities.

Biomedical Field Service Engineer

<h3>Job Description</h3>
Job Title: Principal Medical Device Engineer
Location: New Albany OH
Duration: 12 Months
 
Description:
Ideal candidate: 10 YOE.
Onsite AOH - Monday - Friday - Standard 8-5
Occasional need to have candidates work later into the day due to occasional set up that may be needed. Approximately 1-2x per month.
 
Pre planned travel abroad. !!!CANDIDATES MUST BE ABLE TO TRAVEL INTERNATIONALLY!!!
 
Lead teams in the development of drug delivery devices. Scope includes a wide range of devices, such as; needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems. The qualified candidate will lead technical teams to ensure successful device development of these mechanical and electro-mechanical medical devices. The Principle Engineer will work closely with team members to develop detailed engineering specifications, device design &amp; development, support verification, validation, and regulatory submissions of these devices. The role of the Principle Engineer is to work within a cross-functional organization to utilize technologies and methodologies that support short-cycle robust device development. Responsibilities: - Work cross-functionally with individuals and project teams in Marketing, Operations, and Development - Create and assess product requirements to determine technical coverage and proper integration different subsystems. - Create and execute to project plans and schedules - Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related product development documents for assigned projects. - Provide deep technical assistance for junior engineers. Skills: - BS in Engineering and previous experience in a medical device industry - 10 years current experience with engineering processes and procedures. - Led projects from development through the 510k and PMA approval process. - Strong background in engineering and commercialization of electro-mechanical medical devices. - Experience with material &amp; test specs generation, protocol &amp; report writing, process &amp; test development, prototyping, design verification, DOE/SPC process optimization &amp; validation (IQ, OQ, PQ), FMEA. - Product design/development (design control) from concept to post product launch for Europe (EMEA/CE Mark) &amp; US (FDA/PMA/510k) submissions. - Experience in drug/device combination product design and development - Familiar with the following standards: o Quality System Regulation ? 21CFR820 o Risk Management ? ISO 14971 o EU Medical Device requirements ? Council Directive 93/42/EEC o Medical Electrical Equipment ? EN 60601 - Small scale device assembly experience. - Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations. - Strong problem solving, risk assessment, and risk management skills. - Must be capable of working on multiple projects in a deadline driven environment. VERY IMPORTANT NOTE: Qualified candidates with either a strong Electrical Engineering, Mechanical Engineering, OR Engineering background need apply and will be considered!!!

Biomedical Principal Engineer

<h3>Job Description</h3>
Job Description
Oakwood Laboratories is looking to add to their Formulation Research and Development Team!
This is an excellent opportunity for those interested in advancing their career at a technology-based pharmaceutical company. You will focus on development of sustained release microsphere projects in various stages of development. You will support projects through pre-formulation laboratory experiments and studies, product formulation testing, and process scale up ranging from laboratory to pilot scale. This role will require you to work as part of small multi-disciplinary technical teams on sustained release injectable drug development projects and you will have direct input on solving complex problems and contributing to project success. Become part of the Oakwood Labs team and advance your career with an industry leader in injectable pharmaceutical development.
Essential job functions include:
<ul>
<li>Formulate batches in a laboratory and pilot plant setting, using complex manufacturing processes to design and improve microsphere products</li>
<li>Develop and optimize new innovative processes and technologies for use in formulation development and manufacturing</li>
<li>Present analyses and recommendations in product development team meetings</li>
<li>Collaborate with team members from multiple departments within the company and with external clients to achieve project and company goals</li>
<li>Work in an FDA-regulated environment and adhere to Standard Operating Procedures (SOPs)</li>
</ul>
Attributes required include:
<ul>
<li>Bachelor of Science, Masters, or PhD Degree in Biomedical or Chemical Engineering or closely related science field with chemistry and mathematics in coursework</li>
<li>Basic lab skill obtained from college science labs, internships, or through one year of industry experience</li>
<li>Desire to learn and grow within a team-oriented environment</li>
<li>Good documentation and written and oral communication skills</li>
<li>Time management skills, attention to detail, and ability to work efficiently to meet company deadlines</li>
</ul>
About Oakwood
Oakwood Laboratories is a privately owned specialty pharmaceutical company focused on the design, development and commercial manufacture of sterile injectable sustained release pharmaceuticals. This unique class of products delivers therapeutic levels of drug to patients over days, weeks, months or even years with a single intramuscular or subcutaneous injection. Products of this class have extremely high commercial potential.

Biomedical Engineer/Chemical Engineer

<h3>Job Description</h3>
Job DescriptionCompany Description 
Brainlab revolutionized digital medical technology with the introduction of software for radiosurgery and surgical navigation. Today, Brainlab is an industry leader in digital surgery, radiotherapy and integrated operating rooms.
Serving physicians, medical professionals and patients in 6,000+ hospitals in 121&nbsp;countries, we’re transforming healthcare to improve the lives of patients everywhere.
We employ over 2,000 people in 25 locations worldwide. Close-knit teams made of talented, curious and authentic people are working together toward a common goal.
Together we’re dedicated to making an impact.
Sound like you?
Join and grow with us.
Job Description 
•&nbsp;&nbsp; &nbsp;Provide on-site consulting and guidance to physicians and Operating Room (OR) personnel by evaluating options and problem-solving during surgery in order to maximize Brainlab product efficiency and usage •&nbsp;&nbsp; &nbsp;Manage and maintain install base, including basic 3rd Party integrations •&nbsp;&nbsp; &nbsp;Analyze and resolve product issues for Brainlab systems at assigned Account(s) via Salesforce through detailed analysis and utilization of critical thinking via technical training and documentation •&nbsp;&nbsp; &nbsp;Utilize engineering expertise to contribute to the quality improvement process by recommending product modifications •&nbsp;&nbsp; &nbsp;Provide clinical case coverage &amp; support for Complex Cases and Go Live launches (based on availability) •&nbsp;&nbsp; &nbsp;Manage the process of driving customer utilization, especially via unique workflows and special applications •&nbsp;&nbsp; &nbsp;Act as escalation point for clinical regional issues •&nbsp;&nbsp; &nbsp;Direct and assist Radiology staff in performing necessary scans prior to surgery •&nbsp;&nbsp; &nbsp;Educate/train physicians and hospital personnel, including OR staff, Radiology, Central Sterile Processing, Biomedical and Information Technologies staff, on the use of Image Guided Surgery (IGS) products and services&nbsp; •&nbsp;&nbsp; &nbsp;Develop and conduct training programs for hospital staff enabling them to implement in-house training •&nbsp;&nbsp; &nbsp;Act as primary customer liaison, maintaining contact with customer, assessing satisfaction and usage levels and providing recommendations on this process •&nbsp;&nbsp; &nbsp;Work with the Application Consultant to increase revenue via the sale of spare parts, upgrades, contract renewal, etc. •&nbsp;&nbsp; &nbsp;Work closely with the Application Consultant, Area Account Manager, and Marketing Manager on market transparency, upgrade initiatives, demo/evaluations, and Research &amp; Development (R&amp;D) projects •&nbsp;&nbsp; &nbsp;Attend meetings and trade shows to demonstrate and promote IGS products and services •&nbsp;&nbsp; &nbsp;Keep abreast of developments regarding Brainlab and competitive IGS products and services via ongoing training and individual research and analysis •&nbsp;&nbsp; &nbsp;Collaborate and strategize with Regional Support Manager to provide regular content for team calls/meetings (e.g. provide clinical knowledge transfer, share best practices, interesting cases or case set-ups, etc.) •&nbsp;&nbsp; &nbsp;Maintain Salesforce documentation of all working hours&nbsp; •&nbsp;&nbsp; &nbsp;Attend IGS Continuing Education annually and maintain annual product certification competency
- Salary Range 65-85K.
 Notwithstanding the foregoing, nothing in this job description alters your at-will employment status. Additional duties may be assigned in the discretion of Brainlab.
Qualifications 
<ul>
<li>B.S. in Biomedical Engineering, Biomechanical Engineering, Bioengineering, Clinical Engineering, or Nursing required</li>
<li>1-3 years minimum experience in a technical support role preferably for a healthcare company or Provider</li>
<li>1-2 years minimum sales experience with healthcare company preferred</li>
<li>Knowledge of surgical procedures, anatomy and medical terminology preferred</li>
<li>Proficient in the use of PC software applications including Microsoft Office</li>
<li>Self-motivated, detail oriented and a proven history of ability to make independent decisions</li>
</ul>
 Additional Information 
In return for the experiences listed above we will provide a business casual environment, competitive compensation package including medical, dental, life, LTD, STD, and matching 401k benefits and much more. Visit us at:&nbsp;<a href="http://www.brainlab.com" target="_blank">www.brainlab.com</a>
Brainlab, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. Brainlab participates in E-Verify, more information can be found&nbsp;here. To also review the EEO Law Poster, please&nbsp;click here.
If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to&nbsp;<a href="mailto:us.hr@brainlab.com" target="_blank">us.hr@brainlab.com</a>.

Biomedical Engineer (Clinical Specialist)

<h3>Job Description</h3>
This position is responsible for the repair, maintenance, calibration, and technical support of diagnostic imaging equipment. The Biomedical Imaging Engineer ensures equipment uptime, regulatory compliance, and supports clinical departments in delivering safe and effective patient care.
 
Key Responsibilities
Perform preventive and corrective maintenance on imaging systems including:
<ul>
<li>MRI: Philips Ingenia, Achieva</li>
<li>CT: Philips Brilliance 64, Brilliance Big Bore</li>
<li>Cath Lab: Philips Allura Xper</li>
<li>Additional modalities: X-ray, R&amp;F, mammography, ultrasound, CR, portables, C-arms</li>
<li>Provide high-level technical support and training to clinical departments.</li>
<li>Maintain service documentation and ensure compliance with Joint Commission, FDA, and internal policies.</li>
<li>Coordinate with vendors and OEMs for escalated service and upgrades.</li>
<li>Participate in equipment installations, evaluations, and lifecycle planning.</li>
</ul>
Qualifications
<ul>
<li>Associate’s Degree in Biomedical Equipment Technology, Electronics Technology, or equivalent military/technical training.</li>
<li>3–8 years of experience repairing and maintaining imaging modalities (depending on level).</li>
<li>Phillips OEM certification.</li>
<li>CBET certification is desirable.</li>
<li>Strong troubleshooting skills and understanding of imaging workflows.</li>
<li>Excellent communication and documentation abilities.</li>
</ul>
Preferred Experience
<ul>
<li>Experience with PACS/RIS integration and DICOM standards.</li>
<li>Familiarity with hospital safety protocols and regulatory standards.</li>
<li>Ability to work independently and manage multiple priorities.</li>
</ul>

Biomedical Imaging Engineer

<h3>Job Description</h3>
Title: Product Engineer
Location: Houston, TX
Duration: 24+ Months 
Responsibilities: 
 
- Work with Cataract and Vitreoretinal R&amp;D groups on development projects resulting in achieving R&amp;D’s project goals. Tasks include supplier evaluation/qualification, component qualification, managing prototype builds, assuring assembly process is developed and documented, assure BOM’s are entered and maintained correctly, assure product costs are accurate and rolled, conduct Production Readiness Review.
 - Support Product transfer projects either into or out of plant.
 - Identify and qualify alternate materials and/or components for either risk mitigation or because of obsolescence.
 - Maintain adequate supply of purchased components through contact with Procurement and the Suppliers. Qualify tooling and equipment as required to assure capacity.
 - Address any component or product quality issue assigned, determining root cause and completing corrective action.
 - Address any requests from other departments related to BOM’s and components.
 - Manage product labeling.
 - Identify and qualify Cost Improvements.
 - Communicates clearly.
 - Speaks/writes English.
 - Works well with others.
 - Has leadership capability and is self starter.
 - Ability to learn and retain many complex processes quickly.
 - Focuses on detail/quality.
 - Experience writing technical protocols/reports.
 - Ability to use MS Word/Excel/PowerPoint/Project.
 - Root cause analysis experience to determining cause of issues.
 - Experience in Medical Device industry - Manufacturing / Design / Quality Engineering fields- preferred.
 - Masters in engineering or scientific discipline preferred.

Product Engineer (Biomedical)

<h3>Job Description</h3>
Job title: Product Engineer I
Location: Houston, TX (onsite)
Duration: 24 months
 
Job Description:
Work with Cataract and Vitreoretinal R&amp;D groups on development projects resulting in achieving R&amp;D’s project goals. Tasks include supplier evaluation/qualification, component qualification, managing prototype builds, assuring assembly process is developed and documented, assure BOM’s are entered and maintained correctly, assure product costs are accurate and rolled, conduct Production Readiness Review.
Support Product transfer projects either into or out of plant.
Identify and qualify alternate materials and/or components for either risk mitigation or because of obsolescence.
Maintain adequate supply of purchased components through contact with Procurement and the Suppliers. Qualify tooling and equipment as required to assure capacity.
Address any component or product quality issue assigned, determining root cause and completing corrective action.
Address any requests from other departments related to BOM’s and components.
Manage product labeling.
Identify and qualify Cost Improvements.
 
Communicates clearly.
Speaks/writes English.
Works well with others.
Has leadership capability and is self starter.
Ability to learn and retain many complex processes quickly.
Focuses on detail/quality.
Experience writing technical protocols/reports.
Ability to use MS Word/Excel/Powerpoint/Project.
Root cause analysis experience to determinine cause of issues.
Experience in Medical Device industry - Manufacturing / Design / Quality Engineering fields- preferred.
Experience in an engineering or scientific R&amp;D or manufacturing environment preferred.
 
Masters of Science in Engineering or scientific discipline preferred.

Product Engineer I (Biomedical)

<h3>Job Description</h3>
Job Description
Job Title
Biomedical Clinical Engineer

Location
Veterans Administration
Danville, IL

Description
The Biomedical Engineer is responsible for maintaining and managing medical equipment, ensuring it meets regulatory standards, and supporting healthcare operations. This role involves overseeing a hospital biomedical equipment program, leading a team, and acting as a subject matter expert in the field of biomedical engineering. The Biomedical Engineer will provide technical expertise on medical equipment, from initial concept to effective implementation, while ensuring safety and compliance with healthcare standards and regulations. Essential Duties and Responsibilities
· Manage a hospital biomedical equipment program, ensuring compliance with healthcare standards and regulatory agencies (e.g., VHA, TJC, SMDA).
· Oversee the medical equipment management program, including conducting hazard investigations and managing recalls and safety alerts.
· Act as a subject matter expert in biomedical engineering, supporting specialized clinical technology, including system administration, training, quality assurance, and life-cycle management.
· Advise clinical and administrative staff on medical technology, including emerging technologies, ensuring long-term viability, compatibility, and safety.
· Apply project management principles to the deployment of medical equipment and health information technologies.
· Conduct capital asset and infrastructure planning for medical equipment, including the installation and implementation of complex medical devices.
· Develop and manage a continuing education program addressing the safe and effective use of medical technology.
· Collaborate with stakeholders at various levels of the organization to ensure effective communication and teamwork.
· Ensure compliance with regulatory requirements from agencies such as the International Standard Organization and healthcare industry regulatory bodies.
Travel Minimal travel may be required. Qualifications
· Bachelor's degree or higher in Engineering or Certification as a Clinical Engineer (CCE).
· Minimum of 3 years of hospital or healthcare experience maintaining medical equipment.
· Minimum of 3 years of supervisory experience managing a biomedical equipment program in a hospital.
· Strong knowledge of computer-based medical systems, networking protocols, and information security as applied to medical technology within the VHA.
· Competency in medical equipment management, including compliance with healthcare standards, safety, and recall programs.
· Ability to manage the entire life-cycle of medical technology, from initial concept to implementation, while advising on viability, safety, and long-term suitability.
· Strong project management skills related to medical equipment and health information technologies.
· Knowledge of regulatory requirements and industry standards, including those set by the International Standard Organization.
· Excellent communication and collaboration skills with technical and professional staff.
· Must provide documentation of eligibility to legally work in the United States.
· Must be able to pass client background screening for security clearance.
Work Environment This role is based in a hospital setting, with exposure to medical equipment and clinical environments. The Biomedical Engineer will interact with clinical, administrative, and technical staff to ensure the proper functioning of medical technology. Physical Demands This role may require the physical ability to inspect, install, and maintain medical equipment, including lifting and maneuvering devices as needed. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Salary
· $ 45.67 - $ 53.74 per hour
· $ 95,000.00 - $111,779.20 Annualized
Benefits
· 401K Employer Matching
· PTO
· Holidays
· Health /Dental/Vision Insurance
· Employer-paid Life and AD&amp;D Insurance
· Employee-paid voluntary benefits
· Employee development resources
Equal Opportunity Employer Capital i is an equal opportunity employer. We prohibit discrimination and harassment of any kind based on any protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. Capital i makes hiring decisions based solely on qualifications, merit, and business needs at the time. Capital i is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application process. If you need assistance or an accommodation due to a disability, you may contact us at <a href="mailto:recruiting@capitali.us" target="_blank">recruiting@capitali.us</a>.

Biomedical Clinical Engineer

<h3>Job Description</h3>
Job Description
Select Laboratory Partners, a clinical/toxicology laboratory management company, located in Greensboro, NC is seeking an entry level Biomedical engineer technician. The biomedical engineer will work as a member of a highly specialized expert team under close supervisor of Senior BMET to repair, calibrate and maintain basic clinical laboratory equipment to include Hematology and Chemistry instruments. Extensive training is provided. Position is full time Monday - Friday and will include some overnight travel. Medical, dental and vision benefits are an option. Company paid $50K life insurance policy.
Duties include:
<ul>
<li>Repair, install, maintain, calibrate, and inspect a range of diagnostic instrumentation and equipment</li>
<li>Perform preventive maintenance and electrical safety testing</li>
<li>Diagnose, correct, and document system and equipment malfunction</li>
<li>Provide technical assistance and instruction to personnel on equipment operation and maintenance</li>
<li>Perform related duties as assigned</li>
<li>Expected to participate in meetings, seminars, training, workshops and conferences as required</li>
</ul>
Knowledge, Skills and Abilities:
<ul>
<li>Knowledge of electronic theory, technology and test equipment</li>
<li>Knowledge of color code conventions used in component and wiring markings</li>
<li>Ability to comprehend instructions and effectively communicate</li>
<li>Ability to lift 50 pounds of equipment; push/pull equipment cars; and to kneel, stand, bend and reach during equipment repair</li>
<li>Skill in testing electronic equipment</li>
<li>Skill in manual dexterity, hand-to-eye coordination and color vision</li>
</ul>
Education and experience:
Associates degree in electronic or biomedical equipment technologist with minimum of six months experience in medical equipment repair and maintenance. Medical laboratory technician (MLT) with Associates degree and a desire to learn a new level of laboratory science will be considered. In addition, individuals with a combination of education and experience will be considered. Background screening will be performed. resume to include three references may be submitted to <a href="mailto:jbrown@slplabs.com" target="_blank">jbrown@slplabs.com</a>.
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