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Live In Pharmaceutical Biomedical Engineer Jobs (NOW HIRING)

Aptive

Biomedical Engineer / Clinical Engineer

A Bachelor's degree or higher in Engineering or Certification as a Clinical Engineer (CCE). * A ... biomedical engineering, directly supporting specialized clinical technology, including service ...

Insight

Biomedical Engineer

Chicago, IL · On-site

$30 - $40/hr

These duties are to be performed in a highly confidential manner, following the mission, values ... Minimum 3 years' experience working with biomedical equipment in a clinical engineering environment.

Blue Water Thinking

Biomedical Engineer / LMDI SME

As a Biomedical Engineer, you will play a pivotal role in managing our medical equipment program and ensuring the safety, functionality, and compliance of medical technology within our healthcare ...

Blue Water Thinking

Biomedical Engineer / LMDI SME

As a Biomedical Engineer, you will play a pivotal role in managing our medical equipment program and ensuring the safety, functionality, and compliance of medical technology within our healthcare ...

3D LifePrints

Biomedical Engineer (USA)

Houston, TX · On-site +1

We are looking for a passionate Biomedical Engineer to join our growing team and help design ... In this role, you will transform medical imaging data into custom surgical cutting and drilling ...

Prestige Brands

Sr. Biomedical Engineer

Tarrytown, NY · On-site

As a Senior Biomedical Engineer, you will work closely with cross-functional teams in our corporate ... Your expertise in biomechanics, human factors engineering, and device performance will support ...

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Live In Pharmaceutical Biomedical Engineer information

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How much do live in pharmaceutical biomedical engineer jobs pay per year?

As of Sep 2, 2026, the average yearly pay for live in pharmaceutical biomedical engineer in the United States is $94,807.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $116,000.00 per year, depending on experience, location, and employer.

What is a live in pharmaceutical biomedical engineer?

Live In Pharmaceutical Biomedical Engineers are professionals who reside on-site at pharmaceutical or biomedical facilities to oversee, maintain, and improve biomedical equipment and systems. Their role combines expertise in engineering with a deep understanding of pharmaceutical processes, ensuring that all equipment operates efficiently, safely, and in compliance with regulations. Being on-site allows them to quickly respond to technical issues, support ongoing research or production, and collaborate closely with other staff. This position is especially valuable in facilities requiring constant monitoring or rapid response to equipment malfunctions. Live-in arrangements are less common but critical in certain high-demand or specialized environments.

What are some unique challenges faced by live in pharmaceutical biomedical engineers, and how can candidates prepare for them?

Live In Pharmaceutical Biomedical Engineers often face the challenge of balancing on-site technical responsibilities with the demands of living within the facility, which may require extended hours or being on-call for urgent equipment issues. Candidates should be prepared for a dynamic work environment where collaboration with healthcare professionals and facility staff is frequent, especially during critical maintenance or troubleshooting. Building strong communication skills and being adaptable to non-traditional work schedules will help candidates thrive in this setting. Additionally, staying updated with the latest biomedical regulations and technologies is key to ensuring patient safety and regulatory compliance.

What are the key skills and qualifications needed to thrive as a live in pharmaceutical biomedical engineer, and why are they important?

To thrive as a Live In Pharmaceutical Biomedical Engineer, you need a solid background in biomedical engineering, pharmaceutical sciences, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with laboratory equipment, process automation systems, and quality assurance protocols is essential, along with certifications like Six Sigma or GMP training. Strong problem-solving abilities, effective communication, and adaptability help you excel in dynamic environments and collaborate with multidisciplinary teams. These skills ensure safe, efficient development and maintenance of pharmaceutical technologies, directly impacting product quality and patient safety.

What is the difference between Live In Pharmaceutical Biomedical Engineer vs Pharmaceutical Biomedical Engineer?

AspectLive In Pharmaceutical Biomedical EngineerPharmaceutical Biomedical Engineer
CredentialsTypically requires biomedical engineering degree, certifications in medical device safety, and pharmaceutical industry knowledgeRequires similar biomedical engineering degree, certifications in medical device regulation, and pharmaceutical industry experience
Work EnvironmentResidential setting, often in healthcare or pharmaceutical facilities, providing on-site supportOffice, laboratory, or manufacturing plant environment, with occasional on-site visits
Employer & Industry UsageUsed by pharmaceutical companies, healthcare facilities, and biomedical service providers offering on-site supportCommon in pharmaceutical manufacturing, research labs, and medical device companies

The main difference is that a Live In Pharmaceutical Biomedical Engineer resides on-site, providing continuous support, while a Pharmaceutical Biomedical Engineer typically works in a standard office or lab setting. The live-in role emphasizes on-site presence and immediate response, whereas the standard role involves scheduled visits and remote support.

Can live in pharmaceutical biomedical engineers work in pharmaceutical companies?

Yes, live-in pharmaceutical biomedical engineers can work in pharmaceutical companies, where they typically focus on maintaining and improving medical equipment, ensuring regulatory compliance, and supporting research and development. Their skills in biomedical technology, troubleshooting, and equipment calibration are valuable in such environments.

Where is the best place to live as a live in pharmaceutical biomedical engineer?

The best place for a live-in pharmaceutical biomedical engineer is typically in regions with a strong healthcare and pharmaceutical industry presence, such as areas with major biotech hubs or medical device manufacturing centers. Proximity to research institutions, hospitals, and manufacturing facilities can also enhance career opportunities and work-life balance. Additionally, locations with supportive housing options and good quality of life are beneficial for live-in roles in this field.

What cities are hiring for Live In Pharmaceutical Biomedical Engineer jobs?

Cities with the most Live In Pharmaceutical Biomedical Engineer job openings:

What are the most commonly searched types of Pharmaceutical Biomedical Engineer jobs?

The most popular types of Pharmaceutical Biomedical Engineer jobs are:

What states have the most Live In Pharmaceutical Biomedical Engineer jobs?

States with the most job openings for Live In Pharmaceutical Biomedical Engineer jobs include:

Live In Pharmaceutical Biomedical Engineer jobs near you

Biomedical Engineer / Clinical Engineer

Aptive

Remote

Full-time

Re-posted 24 days ago

Aptive Environmental rating

5.6

Company rating: 5.6 out of 10

Based on 39 frontline employees who took The Breakroom Quiz

30th of 35 rated pest control companies

Job description

Job Summary
Aptive is seeking a Biomedical Engineer / Clinical Engineer to support the Department of Veterans Affairs (VA) under the Biomedical Engineering Technical Professional Support Services (BETPSS) program. This position provides engineering expertise for the lifecycle management, integration, evaluation, and sustainment of medical technologies used throughout VA healthcare facilities.
The Biomedical / Clinical Engineer supports the planning, acquisition, implementation, and optimization of medical equipment and clinical systems to ensure safe, effective, and reliable operation in support of patient care. The role combines engineering analysis, technical oversight, and collaboration with clinical staff, biomedical technicians, IT personnel, and equipment manufacturers.
The engineer assists VA Biomedical Engineering leadership with complex troubleshooting, technology assessments, risk management, regulatory compliance, and modernization initiatives involving diagnostic, therapeutic, and networked medical systems.
Primary Responsibilities
  • Provide engineering support for the lifecycle management of medical devices and clinical systems across VA healthcare facilities.
  • Evaluate, test, and analyze medical equipment performance to ensure safety, reliability, and compliance with regulatory and VA biomedical engineering standards.
  • Support planning, specification development, and technical evaluation for acquisition of new medical equipment and systems.
  • Assist with installation planning, commissioning, and acceptance testing of medical equipment and clinical systems.
  • Provide advanced technical troubleshooting and root-cause analysis for complex equipment failures or system integration issues.
  • Support integration of medical equipment with hospital networks and clinical information systems.
  • Collaborate with biomedical technicians, IT personnel, clinicians, and vendors to resolve technical issues and optimize equipment performance.
  • Assist in development and review of equipment maintenance strategies, service contracts, and lifecycle replacement planning.
  • Ensure compliance with regulatory and safety requirements including FDA, Joint Commission, radiation safety, and VA policies.
  • Support cybersecurity and risk management initiatives related to network-connected medical devices.
  • Maintain documentation of engineering analyses, equipment evaluations, and technical recommendations.

Minimum Qualifications
  • A Bachelor's degree or higher in Engineering or Certification as a Clinical Engineer (CCE).
  • A minimum of three years of hospital or healthcare experience maintaining medical equipment or managing a hospital medical equipment program.
  • Demonstrated knowledge of concepts related to computer based medical systems, networking protocols, and information security as it applies to medical technology within VHA.
  • Demonstrated competency in the ability to conduct a medical equipment management program that is compliant with applicable healthcare standards and regulatory agencies; ability to develop a curriculum for a continuing education program that address the safe and effective use of medical technology; ability to manage a recall and safety alert program for medical devices, including medical device hazard investigations, to assure compliance with patient safety goals, Safe Medical Device Act (SMDA), and JC requirements; ability to conduct capital asset and infrastructure planning for medical equipment spanning initial concept, installation, and effective implementation of complex medical equipment; ability to function as the subject matter expert in the field of biomedical engineering, directly supporting specialized clinical technology, including service, system administration, training, quality assurance, and life-cycle management; ability to effectively advise clinical and administrative staff on medical technology, including existing and emerging technology, which addresses viability, long-term suitability, compatibility, and/or safety; to apply project management principles to deployment of medical equipment and health information technologies.
  • Demonstrated skill in in communicating and working collaboratively with key stakeholders, including technical and professional staff at various levels of the organization.
  • Understanding of regulatory agencies' requirements, industry regulatory requirements and International Standard Organization standards.
  • (OPTIONAL) Experience designing, developing, and implementing clinical system interfaces with electronic health records, ensuring compliance with relevant standards and protocols (e.g., HL7, FHIR, DICOM).

About Aptive
Aptive partners with federal agencies to achieve their missions through improved performance, streamlined operations and enhanced service delivery. Based in Alexandria, Virginia, we support more than a dozen agencies including Veterans Affairs, Transportation, Defense, Homeland Security and the National Science Foundation.
We specialize in applying technology, creativity and human-centered services to optimize mission delivery and improve experiences for millions of people who count on government services every day.
Founded: 2012
Employees: 300+ nationwide
EEO Statement
Aptive is an equal opportunity employer. We consider all qualified applicants for employment without regard to race, color, national origin, religion, creed, sex, sexual orientation, gender identity, marital status, parental status, veteran status, age, disability, or any other protected class.
Veterans, members of the Reserve and National Guard, and transitioning active-duty service members are highly encouraged to apply.

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