2

Remote International Biomedical Engineer Jobs in Kansas

$128K - $169K/yr

Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core ... Bachelor's degree in science, toxicology, pharmacology, engineering or related field; Advanced ...

This role is not eligible for remote work. WHAT YOU'LL DO * Interpret and apply international ... Analyze Engineering Change Orders (ECO) relating to product changes and make recommendations for ...

... international engineering, consulting, and infrastructure firm. While our name has changed, our ... remote opportunities where business needs allow • Life insurance and disability coverage ...

... engineers or other specialized positions * You thrive in a fast-moving, wear-multiple-hats startup ... You have worked in international, remote-first environments and have experience hiring in multiple ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

As a MasTec company, we maintain international capabilities and strategic partnerships throughout ... Remote #LI-LV1 Qualifications: Qualifications * B.S. in Construction Management, Engineering, or ...

Showing results 21-40

Remote International Biomedical Engineer information

What is a remote international biomedical engineer?

A Remote International Biomedical Engineer is a professional who works from a location outside of a traditional office or laboratory, often from another country, to support the design, development, maintenance, and troubleshooting of medical equipment and devices. Their responsibilities typically include collaborating with global teams, providing technical support to healthcare facilities, ensuring regulatory compliance, and assisting with product installations and training remotely. This role requires strong communication skills, technical expertise in biomedical engineering, and familiarity with international standards and regulations. Remote work allows them to assist clients and colleagues across different countries without needing to be physically present.

What are the key skills and qualifications needed to thrive as a remote international biomedical engineer?

To thrive as a Remote International Biomedical Engineer, you need a strong background in biomedical engineering principles, troubleshooting medical devices, and typically a relevant engineering degree. Familiarity with industry-standard tools such as CAD software, medical device regulations (FDA, CE), and remote collaboration platforms is essential. Excellent problem-solving, cross-cultural communication, and self-motivation are standout soft skills for this role. These skills ensure effective design, compliance, and support of medical technologies across diverse global environments while working remotely.

How does a remote international biomedical engineer collaborate effectively with global teams and clients across different time zones?

As a Remote International Biomedical Engineer, collaboration with colleagues and clients worldwide is typically managed through virtual meetings, project management platforms, and clear communication protocols. Flexibility in scheduling is often necessary to accommodate time zone differences, and regular updates are essential to keep all stakeholders aligned. Building strong relationships through proactive communication and cultural sensitivity helps ensure smooth teamwork and project success. Many organizations also provide tools and resources to support seamless international collaboration, such as shared documentation systems and multilingual support.

What is the difference between Remote International Biomedical Engineer vs Remote International Medical Device Technician?

AspectRemote International Biomedical EngineerRemote International Medical Device Technician
Required CredentialsBiomedical engineering degree, certifications in medical device regulationTechnical certifications, device-specific training
Work EnvironmentDesign, development, and testing of medical devices remotelyInstallation, maintenance, and troubleshooting remotely
Employer & Industry UsageHospitals, medical device companies, research institutionsMedical device manufacturers, healthcare providers

Remote International Biomedical Engineers focus on designing and developing medical devices, often requiring engineering degrees and regulatory knowledge. In contrast, Remote International Medical Device Technicians primarily handle installation, maintenance, and troubleshooting of devices. Both roles are essential in healthcare technology, but they differ in responsibilities and skill sets.

What are the most commonly searched types of International Biomedical Engineer jobs in Kansas?

The most popular types of International Biomedical Engineer jobs in Kansas are:

What are popular job titles related to Remote International Biomedical Engineer jobs in Kansas?

For Remote International Biomedical Engineer jobs in Kansas, the most frequently searched job titles are:

What job categories do people searching Remote International Biomedical Engineer jobs in Kansas look for?

The top searched job categories for Remote International Biomedical Engineer jobs in Kansas are:

Director, Regulatory Affairs

Veristat

Remote

$128K - $169K/yr

Full-time

Medical, Retirement

Posted 6 days ago


Job description

Job Description:

Director, Regulatory Affairs

Director Regulatory Affairs, responsible for strategic and operational regulatory consulting for client companies. The Director RA will be client facing and will be responsible amongst others for:

  • Strategic Advice to clients, with focus on early development through to NDA/ BLA
  • Independent preparation of regulatory documentation such as US IND, NDA/BLA modules, ODD, Fast track / other designations, FDA advice requests.
  • Scientific Interaction with internal cross functional teams
  • Client facing & Agency point of contact: Interaction with clients and FDA, lead interactions with Health Authorities
  • Internal BD & marketing facing role
Make an Impact at Veristat!
Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.
  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture - 70% remote workforce, 66% women-led teams
Learn more about our core valueshere!
What we offer

- The estimated hiring range for this role is $195K-223K plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

- Benefits vary by location and may include:

  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans
What we look for
  • Bachelor's degree in science, toxicology, pharmacology, engineering or related field; Advanced Scientific degree such as Master's degree, Ph.D. or Pharm.D. preferred, with applied training relevant to clinical trials.
  • 10 years of relevant experience working directly for a CRO/ Pharmaceutical Company, with a minimum 5 years of experience leading regulatory development projects.
  • Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
  • Excellent written and oral communication skills including grammatical and technical writing skills, and familiarity with moderately complex study designs and regulatory requirements that apply to Phase I-IV clinical trials are required.
  • In-depth knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical / biotech companies.
  • Demonstrated ability to lead by example with demonstrated skill for technical and supervisory leadership of staff.
  • Skilled in use of computer software, including Microsoft Word and Microsoft Excel, and ability to learn new applications.
  • Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.