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Remote Google Biomedical Engineering Jobs (NOW HIRING)

TTC, Inc.

Google Workspace Developer

Remote / USA Clearance: Public Trust Job Summary: TTC has an exciting opportunity for a talented and experienced Google Workspace Migration amp; Solutions Developer to lead the technical migration ...

Dark Wolf Solutions

Google Cloud Engineer

Herndon, VA · Remote

$57.25 - $76.50/hr

... engineering tasks. * Developing and maintaining infrastructure as code (IaC) using tools such as ... Experience with DoD/DISA cybersecurity policies This position will be hybrid / remote based out of ...

Dark Wolf Solutions

Google Cloud Engineer

Colorado Springs, CO · Remote

$55 - $73.50/hr

... engineering tasks. * Developing and maintaining infrastructure as code (IaC) using tools such as ... Experience with DoD/DISA cybersecurity policies This position will be hybrid / remote based out of ...

Dark Wolf Solutions

Google Cloud Engineer

Tampa, FL · Remote

$52.75 - $70.50/hr

... engineering tasks. * Developing and maintaining infrastructure as code (IaC) using tools such as ... Experience with DoD/DISA cybersecurity policies This position will be hybrid / remote based out of ...

Dark Wolf Solutions

Google Cloud Engineer

San Antonio, TX · Remote

$50.25 - $67.25/hr

... engineering tasks. * Developing and maintaining infrastructure as code (IaC) using tools such as ... Experience with DoD/DISA cybersecurity policies This position will be hybrid / remote based out of ...

Lexical Intelligence LLC

NLM Cloud Engineer I

Bethesda, MD · Remote

$59.50 - $79.50/hr

... biomedical information sources. Our Natural Language Processing (NLP) and analytics software is ... Engineering, or related fields * Hands-on experience with cloud platforms (Google Cloud, AWS, and ...

Lexical Intelligence

NLM Cloud Engineer I

Bethesda, MD · Remote

$59.75 - $79.75/hr

... biomedical information sources. Our Natural Language Processing (NLP) and analytics software is ... Engineering, or related fields * Hands-on experience with cloud platforms (Google Cloud, AWS, and ...

Opentrons

$90K - $105K/yr

Remote in Boston, MA area Role ID: EN04100066 About Us Opentrons Labworks, Inc. is a disruptive ... Bachelor's degree in Life Sciences, Biotechnology, Biomedical Engineering, Engineering, or a ...

System One

Quality Assurance Engineer

Mahwah, NJ · Remote

$42 - $48/hr

Hybrid - onsite and remote Responsibilities * Provide quality engineering support in quality ... Bachelor's Degree in Biomedical Engineering, Mechanical Engineering, or related field. * 1+ years ...

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Remote Google Biomedical Engineering information

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$41K

$94.8K

$140K

How much do remote google biomedical engineering jobs pay per year?

As of Sep 13, 2026, the average yearly pay for remote google biomedical engineering 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 remote Google biomedical engineer?

A Remote Google Biomedical Engineering job involves working for Google in the field of biomedical engineering from a remote location, rather than being physically present at an office. Professionals in this role typically focus on developing innovative healthcare technologies, analyzing biological data, and collaborating with cross-functional teams to solve medical challenges using engineering principles. As the position is remote, employees use digital tools to communicate, manage projects, and contribute to research or product development from anywhere with internet access. These roles may require a strong background in biomedical engineering, computer science, and experience with medical devices or data analysis.

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

To thrive as a Remote Google Biomedical Engineer, you need a strong background in biomedical engineering, data analysis, and problem-solving, typically supported by a relevant engineering degree. Familiarity with programming languages (such as Python or MATLAB), cloud computing platforms (like Google Cloud), and experience with medical device standards or software are often required. Excellent communication, self-motivation, and collaboration skills help you effectively coordinate with remote teams and stakeholders. These skills ensure successful development of innovative healthcare solutions while maintaining high standards and seamless teamwork in a remote environment.

What are some common challenges faced by remote biomedical engineers working on Google projects, and how can they overcome them?

Remote biomedical engineers at Google often collaborate with interdisciplinary teams across different time zones, which can make communication and project alignment challenging. To overcome these hurdles, it’s important to establish clear channels for regular updates, leverage collaborative tools like Google Workspace, and proactively schedule meetings to accommodate diverse schedules. Staying organized and maintaining transparent documentation helps ensure that everyone stays on the same page, enhancing productivity and reducing miscommunication.

What is the difference between Remote Google Biomedical Engineering vs Remote Medical Device Software Engineer?

AspectRemote Google Biomedical EngineeringRemote Medical Device Software Engineer
Required CredentialsBiomedical engineering degree, certifications in medical device regulationsSoftware engineering degree, certifications in medical device software standards
Work EnvironmentTech companies, healthcare institutions, research labsMedical device companies, healthcare tech firms, regulatory agencies
Industry UsageDevelops medical technologies, diagnostics, imaging systemsDesigns and tests software for medical devices, ensuring compliance

Remote Google Biomedical Engineering focuses on developing medical technologies and diagnostics within tech and healthcare environments, requiring biomedical credentials. In contrast, Remote Medical Device Software Engineers specialize in creating and validating software for medical devices, emphasizing software skills and regulatory standards. Both roles are essential in advancing healthcare technology remotely, but they differ in focus and expertise.

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Remote Google Biomedical Engineering jobs near you
Infographic showing various Remote Google Biomedical Engineering job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 90% Full Time, 6% Part Time, 2% Contract, and 1% Nights. Highlights an 83% Physical, 4% Hybrid, and 13% Remote job distribution, with an average salary of $94,807 per year, or $45.6 per hour.

Associate Director, Device Engineering

OR • On-site, Remote

Kailera Therapeutics, Inc.
See more jobs at Kailera Therapeutics, Inc.external

Full-time

Posted 24 days ago

Key responsibilities

  • Lead combination product development projects from concept through commercialization.

  • Build and execute project plans with risks and milestones, and oversee design verification and validation activities.

  • Partner cross-functionally with various teams to ensure device development aligns with standards, regulations, and stakeholder needs.

Job description

What You'll Do:

We are seeking an experienced Associate Director, Device Engineering, to lead the development and launch of drug-device combination products, with a strong emphasis on autoinjectors, pre-filled syringes, and multidose pens. This role will drive cross-functional collaboration across CMC, quality, regulatory, manufacturing, clinical, and commercial teams to ensure robust product development aligned with meeting patient needs, global standards, and regulatory expectations.

Required location: Waltham, MA (hub-based, onsite 3-4 days per week) OR Remote (home-based, onsite at a hub 1 week every other month).

Responsibilities:

  • Lead combination product development projects (prefilled syringes, autoinjectors, and/or multidose pens) from concept through commercialization
  • Build and execute project plans with clearly defined risks and milestones
  • Develop device and combination product requirements, including user and stakeholder needs and technical requirements, and ensure appropriate engineering translation and subsequent verification and validation of requirements
  • Oversee and ensure compliance with design controls per FDA and ISO 13485 requirements
  • Manage risk management activities in accordance with ISO 14971, including hazard analysis, FMEA, and risk mitigation strategies
  • Drive design verification and validation activities, including test method development, protocol execution, and documentation
  • Oversee human factors and usability engineering efforts, ensuring compliance with FDA guidance and IEC 62366
  • Facilitate design transfer to manufacturing, ensuring smooth transition and scalability
  • Partner cross-functionally with CMC, quality, regulatory, clinical development, commercial/marketing, supply chain, and other key functions to ensure critical inputs are integrated into device development activities
  • Author relevant portions of regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for devices and combination product programs
  • Manage and collaborate with vendors, including Contract Design and Manufacturing Organizations (CDMOs) and suppliers, to ensure components and products meet quality and technical requirements and to integrate deliverables into the project Design History File at various stages of development and manufacturing
  • Manage and collaborate with contract test labs to ensure testing strategy, method validation, and test execution are aligned with relevant standards and quality and technical requirements and integrate testing results into the Design History File
  • Ensure product development aligns with relevant standards including ISO 11608-1, ISO 11040, ASTM D4169, ISO 14971, IEC 62366

Required Qualifications:

  • Minimum of 10+ years of experience in medical device or combination product development, with at least 3 years in a team leadership role
  • Proven experience with autoinjector, pre-filled syringe, or multidose pen development and launch, including authoring clinical and commercial regulatory submissions
  • Deep understanding of design controls, design verification, test method development and validation, risk management, human factors, and design transfer
  • Strong knowledge of applicable regulatory standards and guidance documents
  • Excellent communication, leadership, and cross-functional collaboration skills

 

Preferred Qualifications:

  • Experience working in a regulated pharmaceutical or biotech environment
  • Familiarity with combination product regulations (21 CFR Part 4)
  • Experience with supplier management of external development, testing, and manufacturing partners
  • PMP certification or formal project management training is a plus

Education:

  • Bachelor's degree in mechanical engineering, Biomedical Engineering, or related field. Advanced degree preferred.

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