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Remote Biomedical Product Development Engineer Jobs

SDET, Remote opportunity

Irvine, CA ยท On-site +1

$130K - $145K/yr

Senior SDET Location: Hybrid if local to Irvine, CA. 100% remote if you live more than 30 miles ... Define quality gates for pilot expansion and instrument production monitoring to catch issues early

SDET - 100 % Remote

Cincinnati, OH ยท Remote

$51.25 - $66/hr

Position: SDET Number of openings: 1 Onsite or Remote: Remote - 100% allowable Perm/Contract/CTH ... product requirements and their applicability to product code and test code. They also perform ...

Approval of remote and hybrid work is not guaranteed regardless of work location.For additional ... Atlassian products (e.g., JIRA, Confluence) Your work location will be project-dependent ability ...

New

Software Development Engineer

Livermore, CA ยท On-site +1

$75K - $99K/yr

Whether it's improving products, supporting customers, or positively influencing peers and the ... A role is remote-eligible only when it is listed as "Remote" in the job location.

New

Product Development Lead

Walnut Creek, CA ยท On-site +1

$120K - $180K/yr

Work will focus on (1) identifying strategic pathways for product development, (2) preparing ways ... the engineering team, relay and explain design concepts Why Join * highly creative role in a ...

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Remote Biomedical Product Development Engineer information

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$39.5K

$87.9K

$132.5K

How much do remote biomedical product development engineer jobs pay per year?

As of Jul 14, 2026, the average yearly pay for remote biomedical product development engineer in the United States is $87,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $100,000.00 per year, depending on experience, location, and employer.

What is the difference between Remote Biomedical Product Development Engineer vs Remote Biomedical Research Scientist?

AspectRemote Biomedical Product Development EngineerRemote Biomedical Research Scientist
Required CredentialsBachelor's or Master's in Biomedical Engineering, related field; certifications in product design or regulatory affairsMaster's or PhD in Biomedical Science, Biology, or related field; research certifications
Work EnvironmentCollaborates with engineering, manufacturing, and regulatory teams; focuses on product design and developmentConducts experiments, data analysis, and scientific research; often in labs or remote research settings
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developersResearch institutions, biotech companies, academic labs

The Remote Biomedical Product Development Engineer primarily focuses on designing and developing medical devices and products, working closely with engineering teams. In contrast, the Remote Biomedical Research Scientist conducts scientific research to advance biomedical knowledge. Both roles require relevant degrees and certifications but differ in daily tasks and work environments.

What cities are hiring for Remote Biomedical Product Development Engineer jobs? Cities with the most Remote Biomedical Product Development Engineer job openings:
What are the most commonly searched types of Biomedical Product Development Engineer jobs? The most popular types of Biomedical Product Development Engineer jobs are:
What states have the most Remote Biomedical Product Development Engineer jobs? States with the most job openings for Remote Biomedical Product Development Engineer jobs include:

Human Factors Design Controls Engineer as 100% Remote

Amicis Global

Sunnyvale, CA โ€ข Remote

$74/hr

Contractor

Re-posted 3 days ago


Job description

Job Title:ย Human Factors Design Controls Engineer
Location:ย Remote
Duration:ย 12 Months
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Pay Rate: $64.00 - $74.00/- on W2
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Please Note: Must be comfortable working in the PST time zone.
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Kindly help me out with your most updated resume
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Roles and Responsibilities:
As part of the Intuitive Human Factors team, the Human Factors Design Controls Engineer works closely with fellow HF team members and department leadership and other cross functional partners. The Human Factors Design Controls Engineer is a key contributor to inform, guide development of, and maintain usability engineering documentation produced during product development projects. Responsibilities are focused on comprehensive and timely implementation of task analysis and related risk analysis documents.
This role supports the Human Factors Engineering team with expertise in design controls and helps create usability engineering documentation required for submission to global medical device regulatory agencies.
This role provides dedicated support and subject matter expertise guidance to the broader human factors engineering team serving all business units and reports to a human Factors team lead. For reference, a brief description of each of the business units is as follows.
Support remediation of usability related risk analysis documentation, including revising, editing and reformatting, collating and tracing of task analysis and usability risk analysis document content.
Support definition, release and maintenance of usability related design inputs documentation.
Create and maintain tracing documentation with the Polarion tracing environment to Identify and resolve tracing conflicts and design input orphans in tracing between risks and design inputs/risk controls.
This position is remote, using Intuitive laptop, software and administrative systems.
Qualifications
Skill/Job Requirements:
Minimum Education: BS in Human Factors Engineering, Biomedical Science or Engineering, Systems Engineering, Quality Engineering, Information and Data Science, Cognitive Psychology, Computer Science with human-computer interface (HCI) emphasis, Human Centered Design, or related field.
Minimum of 5 years of related experience with a bachelor's degree in engineering, and have experience design controls, risk remediation, and risk analysis related medical device product development (or related field).
Experience working with Digital project collaboration tools is required. (e.g. Polarion, Agile PDM, Smartsheets etc.).
Background and understanding of MDR regulations and best practices for medical device human factors (e.g. IEC 62366, AAMI HE75, FDA Applying Human Factors and Usability Engineering to Medical Devices).
Excellent verbal communication and presentation skills working within a highly statured communication environment using multiple communication channels (email, text, video conference, instant messaging platforms).
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