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The University of Rochester seeks an experienced, strategic, and collaborative leader to serve as its next Associate Vice President for Human Subject Protection (AVP-HSP).&nbsp; Reporting to the University’s Vice President for Research, the Associate Vice President is responsible for the staff, resources, systems, and policies that enable research involving human subjects, sustaining safety and compliance while advancing knowledge.
Key functions of the Office of Human Subject Projection (OHSP) under the AVP-HSP’s responsibility include <a href="https://www.rochester.edu/ohsp/rsrb/index.html" target="_blank">Research Subject Review Board</a> (RSRB), <a href="https://www.rochester.edu/ohsp/education/index.html" target="_blank">Research Education and Training</a>, and <a href="https://www.rochester.edu/ohsp/quality/index.html" target="_blank">Research Quality Improvement</a>. At any given time, there are more than 2,000 active research studies being conducted by approximately 3,000 investigators, across more than 100 departments, centers, and labs at the University and University of Rochester Medical Center. The AVP-HSP must be forward-thinking and proactive in considering the impact that evolving regulations and external factors may have on University-wide research plans, programs, and operations. They are the University leader in human subject-research risk-assessment and risk-mitigation discussions.
As OHSP is a University-wide resource, the AVP-HSP collaborates with research deans across the University as well as the Office of Research and Project Administration, the Office for Clinical Research, the Clinical and Translational Science Institute, and the Office of General Counsel. Alongside research deans from each school and key members of the Office of the Vice President for Research, the AVP-HSP is a member of the University’s Research Executive Committee. Rochester’s human-subject protection program has been AAHRPP-accredited since 2004.
The AVP-HSP must be a highly visible member of the University community and continuously engaged with University stakeholders, communicating and demonstrating OHSP’s commitment to being a collaborative partner with departments and divisions across the institution. The AVP-HSP ensures that the 14-member OHSP team is likewise knowledgeable, skilled, trained, and engaged in serving the good of the broader University community in thoughtful, thorough, and objective engagements.
The AVP will have well-developed and tested leadership and collaboration qualities, extensive research compliance expertise, and experience working with clinical, translational, and behavioral researchers. They will have the highest level of integrity and will demonstrate a track record of developing, mentoring, and supporting diverse and high-functioning teams.
Viable candidates will have at least 10 years of directly relevant experience, including in positions in which they had supervisory responsibility. If they are not coming from a peer academic or medical institution, they will demonstrate the ability to learn quickly and will have relevant research leadership experience with large, matrixed, and highly complicated organizations. A bachelor’s degree is required; a master’s degree in a field that entails working with human subjects and Certified IRB Professional designation are preferred.
A full version of the position description can be found <a href="https://acrobat.adobe.com/link/review?uri=urn:aaid:scds:US:3228df3d-301b-3fe8-b891-c06a30aa0bed" target="_blank">here</a>.
University of Rochester researchers are among the nation's leaders across virtually every discipline. At the University’s River Campus, research spans a wide array of fields from engineering, the natural and social sciences, the humanities, and education to music and business. The <a href="https://www.urmc.rochester.edu/" target="_blank">University of Rochester Medical Center (URMC)</a> is distinguished in professional education, biomedical research, and clinical care. It is the home of the University’s health research, teaching, and patient care missions, and includes <a href="https://www.urmc.rochester.edu/strong-memorial.aspx" target="_blank">Strong Memorial Hospital</a>, the <a href="https://www.urmc.rochester.edu/cancer-institute.aspx" target="_blank">Wilmot Cancer Institute</a>, <a href="https://www.urmc.rochester.edu/childrens-hospital.aspx" target="_blank">Golisano Children’s Hospital</a>, and affiliated healthcare systems in the region comprising five additional hospitals and numerous clinical locations, as well as long-term care facilities.
The University enrolls over 12,000 undergraduate and graduate/professional students, both domestic and international, and employs over 3,300 full- and part-time faculty. The University of Rochester’s overall annual consolidated budget is approximately $5 billion, including all aspects of URMC.
In FY 2022, the University reported $432 million in research expenditures, denoting the high value placed on scholarship. With over 60 research centers and institutes, the University allows students, faculty, and research staff to pursue their academic goals in an environment that empowers and supports their efforts.
The University of Rochester has retained <a href="https://opuspartners.net/" target="_blank">Opus Partners</a> to support the recruitment of this position. Craig Smith, Partner and Abigail Maynard, Senior Associate, are leading the search. Confidential inquiries, applications, and nominations should be sent by email to Abigail (<a href="mailto:abigail.maynard@opuspartners.net" target="_blank">abigail.maynard@opuspartners.net</a>). The search process will unfold with the greatest possible attention to candidate confidentiality. Required application materials include a resume and cover letter. The cover letter should reflect how qualifications and experience match those described in this leadership profile, including examples of demonstrated commitment to diversity, equity, and inclusion within the context of the AVP-HSP role.
The University of Rochester values diversity and is committed to equal opportunity for persons regardless of age, color, disability, domestic violence status, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion/creed, sex, sexual orientation, or any other status protected by law. Further, the University complies with all applicable nondiscrimination laws in the administration of its policies, admissions, employment, and access to and treatment in University programs and activities.

Associate Vice President for Human Subjects Protection

<h3>Job Description</h3>
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.
1-10 years experience in an engineering or scientific R&amp;D or manufacturing environment preferred.
 
Masters of Science in Engineering or scientific discipline preferred.

Biomedical 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 Title: Senior Engineer/ Engineer Principal
Location: New Albany, OH
Duration: 12+ Months
 
Description
Onsite AOH - Monday - Friday - Standard 8-5
Very occasional need to have candidates work later into the day due to occasional set up that may be needed. Approximately 1-2x per month.
 
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 Principal 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 Principal 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 Systems/Software Engineering background need apply and will be considered!!!

<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>
Job Description
(ID: 2025-1385)
 
Axle Informatics is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations around the globe. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with premier research organizations and facilities including multiple institutes at the National Institutes of Health (NIH) and other public and private organizations. 
Benefits We Offer:
<ul>
<li>100% Medical, Dental &amp; Vision Coverage for Employees</li>
<li>Educational Benefits for Career Growth</li>
<li>Paid Time Off (Including Holidays)</li>
<li>Employee Referral Bonus</li>
<li>401K Matching</li>
<li>Flexible Spending Accounts:
<ul>
<li>Healthcare (FSA)</li>
<li>Parking Reimbursement Account (PRK)</li>
<li>Dependent Care Assistant Program (DCAP)</li>
<li>Transportation Reimbursement Account (TRN)</li>
</ul>
</li>
</ul>
Overview: 
At the intersection of high-throughput drug discovery and cloud-native engineering, we are building the foundational infrastructure for a "lab-in-an-automated-loop". We produce petabyte-scale imaging data across global research sites and are now moving to modernize how that data is processed, analyzed, and stored.
We are not looking for a generalist. We need a specialist who understands that an imaging pipeline is only as good as the scientific data it produces. You will be the technical lead responsible for migrating complex imaging logic into a modular, stateless Nextflow ecosystem that supports consistent scientific decision-making at a global scale.
The Opportunity: Your Impact
We are seeking a Senior Biomedical Imaging Engineer with deep biomedical Imaging expertise. You will be responsible for refactoring high-priority imaging assays and moving them from interactive, platform-dependent workflows into headless, portable, and highly optimized Nextflow processes.
You must be an imaging expert first. You need to understand what is happening to the pixels, how feature tables are derived, and why a specific segmentation mask or QC metric is critical for the downstream science.
What You'll Do:
<ul>
<li>Nextflow Refactoring &amp; Architecture: Identify imaging pipeline components suitable for direct implementation in Nextflow and refactor them into modular, reproducible processes that mirror or improve upon validated behavior.</li>
<li>Deep Imaging Data Analysis: Define and document required inputs, intermediate outputs (segmentation masks, feature tables), and final plate-level summaries, ensuring the engineering supports the scientific intent.</li>
<li>Architect for Heterogeneous Hardware: Design Nextflow configuration profiles that allow identical workflow definitions to run across diverse environments, from high-end GPU clusters (Nvidia L40s) with SLURM to legacy on-premise HPC nodes.</li>
<li>Headless Integration: Lead the development of scripts and wrappers that enable headless execution of imaging logic, integrated directly into a GCP Workflows-based automated control system.</li>
<li>Scientific Validation: Design and execute regression checks to ensure that refactored Nextflow pipelines produce outputs equivalent to legacy systems within strict scientific tolerances.</li>
<li>Modular Pipeline Design: Ensure every step in the pipeline is as stateless and modular as possible to allow for rapid refactoring and reuse across different imaging assays.</li>
<li>Integrate the "Lab Loop": Collaborate with engineers to manage data handoffs between on-premise edge infrastructure and cloud-based system-of-record databases (PostgreSQL/ARC).</li>
</ul>
What You'll Bring (Required Qualifications):
<ul>
<li>A passion for the craft of engineering: you believe that scientific pipelines should be modular, stateless, and elegant.</li>
<li>Advanced Nextflow Mastery: Proven experience architecting and deploying complex, production-grade pipelines in Nextflow for a research or clinical environment.</li>
<li>Imaging Domain Expertise: Professional or academic background in Bioimage Informatics or Imaging Science. You must deeply understand image analysis algorithms, HCS data structures, and spatial metadata.</li>
<li>Scientific Mindset: You have experience defining QC metrics and interpreting scientific outputs for high-throughput imaging.</li>
<li>Infrastructure Fluency: Deep experience with Linux/Unix, HPC schedulers (SLURM), and optimized execution on Nvidia GPU architectures.</li>
<li>Cloud Literacy: Experience working within Google Cloud Platform (GCP) or similar cloud environments for data orchestration and storage.</li>
<li>Containerization Expert: Proficient in using Docker or Singularity to ensure that every step of the imaging process is hermetic and reproducible.</li>
</ul>
What Sets You Apart (Preferred Qualifications):
<ul>
<li>SImA/Signals Familiarity: Experience with Revvity Signals Image Artist (SImA) is a strong plus, though our team already includes dedicated SImA specialists to support your refactoring efforts.</li>
<li>GCP &amp; Cloud Orchestration: Experience with Google Cloud Platform and GCP Workflows for orchestrating "lab-in-the-loop" automation.</li>
<li>Programming Depth: Strong proficiency in Python or C++ for developing custom imaging transformation steps.</li>
<li>Pharma R&amp;D Experience: Experience working with high-throughput assay data and system-of-record databases like PostgreSQL.</li>
</ul>
 
The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment-based age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate.
Accessibility: If you need an accommodation as part of the employment process, please contact <a href="mailto:careers@axleinfo.com" target="_blank">careers@axleinfo.com</a>
Disclaimer: The above is meant to illustrate the general nature of work and level of effort being performed by individual's assigned to this position or job. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job or responsibilities as needed.
This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.

Senior Biomedical Imaging Engineer

<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 Description
The primary responsibility of this position is to provide phone support and assist with troubleshooting, repairing, and testing equipment for all customer sites. This includes validating effectiveness and performing quality control checks. Additionally, the role involves preparing and reconditioning equipment for shipment. There will also be travel to customer locations to install equipment, provide training, diagnose issues, and offer necessary services
Essential Functions and Duties: 
The responsibilities listed below are essential to the role; additional duties may be assigned to meet business needs:
<ul>
<li>Install, train, troubleshoot, repair, and perform preventive maintenance on all company diagnostic equipment, both on-site and off-site.</li>
<li>Provide high-quality phone support by responding to customer inquiries, delivering technical assistance, and training customers on operation, maintenance, and basic troubleshooting.</li>
<li>Ensure timely and effective repairs, along with comprehensive training for operators, to guarantee optimal system performance and high customer satisfaction.</li>
<li>Demonstrate self-motivation, excellent communication skills, and teamwork abilities while being capable of working with minimal supervision.</li>
<li>Develop new test systems and provide recommendations on technical procedures. Evaluate new equipment and assist in creating and writing test procedures, standard operating protocols, and training materials.</li>
<li>Be prepared for national and international travel, which may require up to 50% of your time visiting customer or manufacturer sites.</li>
<li>Be available for occasional off-hours work, including scheduled on-call hours during early mornings, evenings, or weekends as needed.</li>
</ul>
Additional Responsibilities: 
<ul>
<li>Assist with special projects and perform other engineering-related duties as requested.</li>
<li>Maintain a clean work area and maintain standard office equipment in good condition.</li>
<li>Help gather, record, and maintain engineering-specific information, and provide feedback on instrument issues to Engineering, Manufacturing, and Service departments.</li>
</ul>
Qualifications/Requirements:
<ul>
<li>A bachelor's degree in Engineering (Biomedical, Electrical, or Mechanical). </li>
<li>Strong knowledge of instrument systems technology, including mechanical, electrical, chemical, and software components. </li>
<li>Excellent communication skills, with the ability to interact positively and professionally with customers and colleagues. </li>
<li>Strong organizational and problem-solving skills. </li>
<li>Capacity to think and act logically and methodically.</li>
<li>Proficient in Microsoft Office and skilled in using computer-based tools for reporting, email, and general communication.</li>
<li>Ability to resolve complex mechanical, electromechanical, and system issues using technical manuals, publications, and engineering support. </li>
</ul>
Willingness to travel as needed.

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