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Remote Medical Device Jobs in Detroit, MI (NOW HIRING)

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Remote Medical Device information

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How much do remote medical device jobs pay per hour?

As of Aug 29, 2026, the average hourly pay for remote medical device in Detroit, MI is $49.34, according to ZipRecruiter salary data. Most workers in this role earn between $34.76 and $59.04 per hour, depending on experience, location, and employer.

What is a remote medical device?

A remote medical device is a piece of medical equipment that can monitor, diagnose, or treat patients from a distance, often using wireless or internet-connected technology. These devices enable healthcare providers to collect real-time data, track patient health, and even adjust treatments without requiring in-person visits. Common examples include remote heart monitors, wearable glucose meters, and telemedicine-enabled devices. Remote medical devices are increasingly used to improve patient outcomes, especially for those with chronic conditions or limited access to healthcare facilities.

What are remote medical device jobs?

Remote medical device jobs include roles in sales, advertising, programming, manufacturing, and testing of medical equipment. In this role, you may provide guidance and customer support to clinical customers, test the technology used in medical devices, or help fill out paperwork to meet regulatory reporting requirements. While medical device sales, IT, and customer service jobs can often be done remotely, there may be more opportunities for programmers and testers as the use of advanced technology and software becomes more common. Remote posts in the medical device field require computer and communication skills.

What are the key skills and qualifications needed to thrive as a remote medical device specialist, and why are they important?

To excel as a Remote Medical Device Specialist, you need a solid background in biomedical engineering, healthcare technology, or a related discipline, often supported by relevant certifications or a degree. Familiarity with remote monitoring platforms, device integration software, and regulatory standards like FDA or ISO is typically required. Strong problem-solving, communication, and customer service skills help build trust and ensure effective support for healthcare providers and patients. These competencies are crucial for ensuring device safety, compliance, and optimal performance in remote healthcare environments.

What are some unique challenges faced by professionals working remotely in the medical device industry?

Professionals in remote medical device roles often encounter challenges such as ensuring effective communication with cross-functional teams, staying updated on regulatory changes, and managing product support or troubleshooting virtually. Since device demonstrations and technical support may need to be conducted online, strong digital communication skills are essential. Additionally, remote workers must be proactive in maintaining compliance and documentation standards, and they often collaborate closely with quality assurance, regulatory, and product development teams to address issues promptly and efficiently.

What is the difference between Remote Medical Device vs Remote Medical Device Technician?

AspectRemote Medical DeviceRemote Medical Device Technician
CertificationsRegulatory knowledge, medical device complianceTechnical certifications, device troubleshooting
Work EnvironmentDesign, development, regulatory complianceInstallation, maintenance, troubleshooting
Industry UsageManufacturers, healthcare companiesService providers, healthcare facilities

Remote Medical Device roles focus on designing, developing, and ensuring regulatory compliance of medical devices, often involving regulatory knowledge and product development. In contrast, Remote Medical Device Technicians primarily handle installation, maintenance, and troubleshooting of devices in clinical settings. Both roles are essential in the medical device industry but differ in responsibilities, certifications, and work environments.

More about Remote Medical Device jobs

What are the most commonly searched types of Medical Device jobs in Detroit, MI?

The most popular types of Medical Device jobs in Detroit, MI are:

What are popular job titles related to Remote Medical Device jobs in Detroit, MI?

For Remote Medical Device jobs in Detroit, MI, the most frequently searched job titles are:

What job categories do people searching Remote Medical Device jobs in Detroit, MI look for?

The top searched job categories for Remote Medical Device jobs in Detroit, MI are:

What cities near Detroit, MI are hiring for Remote Medical Device jobs?

Cities near Detroit, MI with the most Remote Medical Device job openings:

Remote Medical Device jobs near you
Infographic showing various Remote Medical Device job openings in Detroit, MI as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $102,621 per year, or $49.3 per hour.

Sr Mgr, QA/Quality Engineer, Device & Combination Products

ESPERION THERAPEUTICS INC

Ann Arbor, MI • Remote

Full-time

Medical, Retirement, PTO

Re-posted 2 days ago

Job description

Company Overview

Our Mission: At Esperion, we are working tirelessly to deliver innovative medicines that help patients reach their goals today, tomorrow, and into the future.


Esperion Quality Philosophy: Quality is in all we do because all we do is for our patients. 

Esperion’s passion for quality is an integral part of our company culture and is embedded in every aspect of the organization. We are committed to applying the highest quality standards to develop and deliver safe, effective pharmaceutical products that significantly improve the quality of life for the patients and clinical trial participants we serve.


Esperion is a fully remote‑based company with a corporate headquarters located in Ann Arbor, MI. The Company offers a competitive salary including a performance‑based bonus program, a comprehensive benefits package including a 401(k) matching plan and health insurance, and paid time off and holidays.

Position Title: Senior Manager, Quality Assurance / Quality Engineer – Device and Combination Products

This role is responsible for the quality of assigned suppliers/contract manufacturers to ensure business objectives are met with regards to on time delivery of product while assuring compliance to Esperion requirements, applicable external regulations, and standards. 


This position serves as the Quality Assurance subject matter expert for combination products, ensuring appropriate control strategies are in place for drug substance, drug product, and device components, and partners closely with Quality Control, Regulatory Affairs, Technical Operations, and external partners to maintain inspection readiness.



Preferred Location: Remote – US

Essential Duties and Responsibilities*

  • Provide in‑depth technical and scientific leadership to contract service providers and internal stakeholders related to Quality Engineering for device and combination products.
  • Serve as the primary QA/QE technical and project management liaison with CDMOs and external testing laboratories supporting drug substance, drug product, and device/combination component testing.
  • Review and approve development, release, and stability data for routine manufacturing, investigations, and deviations involving drug substance, drug product, device and combination products.
  • Conduct quality review and approval of critical quality records and documents, including batch records, deviations, investigations, CAPAs, change controls, complaints, risk management, validation protocols and reports, stability documentation, Design History File, and Annual Product Reviews (APR). 
  • Ensure compliance with applicable combination product regulatory requirements, including 21 CFR Parts 4, 210, 211, 820, ISO 13485 and other relevant regulations. 
  • Release 
  • Provide quality oversight of external suppliers and contract manufacturers involved in manufacturing, assembly, filling, testing, and packaging. 
  • Support regulatory submissions and act as the QA/QE lead during FDA, EU, and partner audits and inspections, including those involving combination product or device‑related scope.
  • Support Medical Device Reporting activities.
  • Assist with supplier qualifications and monitoring compliance with Quality Agreements. 
  • Serve as a Quality representative for cross-functional activities supporting device and combination product development and commercial supply. 
  • Partner with QC and Technical Device Engineer on investigations, change controls, CAPAs, and risk assessments.
  • Support qualification of alternate manufacturing sites, laboratories, service suppliers, and device component suppliers.
  • Lead or co‑lead cross‑functional Technical Operations projects and CDMO oversight activities.
  • Support complaint handling and investigation activities. 

*Additional duties and responsibilities as assigned.

Qualifications (Education & Experience)

Required Qualifications

  • Bachelor’s degree in Chemistry, Biology, Engineering, or a related scientific discipline from an accredited college or university.
  • 8+ years of progressive Quality Assurance or Quality Engineering experience within the medical device or drug–device combination product industry.
  • Direct experience supporting medical devices and/or drug–device combination products in a regulated GxP environment.
  • Strong working knowledge of:
    • 21 CFR Parts 210/211 (cGMPs)
    • 21 CFR Part 4 (Combination Products)
    • ISO 13485 and ISO 14971
    • ISTA
    • Applicable elements of 21 CFR Part 820
  • Proven experience managing global external CDMOs and contract testing laboratories.
  • Experience supporting regulatory inspections and audits, including preparation and response activities.
  • Strong project management, communication, and stakeholder‑influencing skills in a matrixed environment.

Preferred Qualifications

  • Experience working within ISO 13485‑aligned quality systems.
  • Experience supporting EU MDR or global device regulatory submissions.
  • Background supporting combination products such as inhalers, prefilled syringes, autoinjectors, or other delivery systems.
  • Experience contributing to CMC sections of U.S. or EU regulatory filings involving combination products.
  • Familiarity with data integrity requirements and lifecycle management of analytical methods for combination products.
  • Experience with electronic Quality Management Systems (e.g., Veeva QMS)
  • Experience setting up and maintaining Design History Files, Risk Management Files, as well as other device and combination product records.

Additional Requirements

  • Proficiency with MS Office, laboratory, and quality systems (LIMS, QMS, EDMS).
  • Demonstrated alignment with Esperion’s values and culture.
  • Ability to work effectively in a fully remote environment.
  • Moderate domestic and international travel required (up to 25% annually).

Apply