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Biomedical Engineering Military Jobs in Michigan

Mechanical, Electrical, Chemical, Biomedical, Aerospace, Computer Engineering, Materials Science ... religion, military or veteran status, or any other characteristics protected by law. Have a ...

Field Service Engineer

Detroit, MI · On-site

$80K - $100K/yr

... biomedical, electrical/electronics, or computer engineering technology; military training; or equivalent combination of education and experience • 2 to 4 years of Ultrasound and/or medical ...

Laser Engineer

Saint Clair, MI · On-site

$65K - $80K/yr

Are you an innovative Field Service Engineer with a passion for cutting-edge technology? Join ... Biomedical Equipment Technology, Electronics, or a similar field; military training in related ...

AS, BS, MS degree, military education, certificate program, current student with less than 12 ... biomedical or electronic equipment. * Analytical and communication skills with the ability to ...

Showing results 21-37

Biomedical Engineering Military information

What are the typical day-to-day responsibilities of a biomedical engineering military?

In a Biomedical Engineering Military role, you can expect to be responsible for the maintenance, calibration, and repair of medical equipment used in military treatment facilities or field environments. Your daily tasks may involve troubleshooting equipment malfunctions, ensuring compliance with safety and performance standards, and conducting routine inspections. You will often collaborate closely with medical staff, logistics personnel, and other technical specialists to support continuous healthcare operations. This position requires the ability to respond quickly to equipment issues and adapt to evolving operational needs, especially during field deployments or emergency situations.

What do biomedical engineers do in the military?

Biomedical engineers in the military design, develop, and maintain medical devices and equipment used in healthcare and field operations. They may work on prosthetics, imaging systems, and life-support devices, often requiring knowledge of electronics, biomechanics, and medical standards. Their role supports both clinical settings and combat environments, ensuring equipment reliability and safety.

What is a biomedical engineering military?

A Biomedical Engineering Military job involves designing, maintaining, and repairing medical equipment used in military settings. Professionals in this role ensure that medical devices function properly in field hospitals, combat zones, and military medical facilities. They may also work on research and development of new technologies to support military healthcare needs. This role requires knowledge of engineering, medical science, and military protocols.

What are the key skills and qualifications needed to thrive as a biomedical engineering military, and why are they important?

To thrive as a Biomedical Engineering Military professional, you need solid knowledge of biomedical equipment, engineering principles, and military protocols, usually supported by a relevant degree or military technical training. Experience with diagnostic and therapeutic device maintenance, repair tools, inventory management systems, and certifications like CBET (Certified Biomedical Equipment Technician) is highly valuable. Strong problem-solving skills, teamwork, adaptability, and effective communication are important soft skills in this field. These abilities ensure mission readiness, equipment reliability, and efficient collaboration in high-pressure military healthcare environments.

What cities in Michigan are hiring for Biomedical Engineering Military jobs? Cities in Michigan with the most Biomedical Engineering Military job openings:
Infographic showing various Biomedical Engineering Military job openings in Michigan as of July 2026, with employment types broken down into 88% Full Time, 8% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution.

Senior Manager, Clinical Diagnostics CDx (Precision Medicine)

Regeneron Pharmaceuticals

Warren, MI

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted yesterday


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical


Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Manager, Clinical Diagnostics to support end-to-end companion diagnostics (CDx) strategy and execution across our therapeutic indications. In this role, you will translate scientific needs into fit-for-purpose assays for global decisions, owning programs from feasibility through validation, registration, launch, and post-market sustainment, while partnering with biomarker, clinical, regulatory, commercial, and IVD collaborators.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

  • Location: Tarrytown, NY

  • Work model/flexibility: Onsite

  • Travel percentage: Up to 5-10% for partner meetings, clinical site visits, and regulatory interactions.

Discover your role:

  • Execute end-to-end CDx strategy, aligning diagnostic milestones with therapeutic clinical development and regulatory timelines

  • Lead cross-functional teams, integrate workstreams, clear obstacles, and provide transparent status reporting to governance bodies and senior leadership

  • Manage IVD partners, negotiating scope, timelines, budgets, and quality, and overseeing co-development and Joint Steering Committees

  • Define assay intent and contribute to target product profiles for CDx platforms (e.g., NGS, PCR, IHC, Immunoassays), driving analytical and clinical validation

  • Embed CDx assays in trials with clinical teams, covering screening/stratification, sampling, site readiness, and lab operations

  • Partner with IVD Regulatory on global submissions (FDA, EU IVDR, PMDA), supporting pre-subs, labeling, and responses

  • Ensure compliance with quality and regulatory frameworks (ISO 13485/14971, CLSI, IVDR, GCP), maintaining documentation and audit readiness

  • Thrive in a fast-paced, multi-tasking environment, bringing strong communication skills to cross-functional collaboration.

This role requires:

  • Advanced degree in molecular biology, pathology, biomedical engineering, or equivalent experience

  • 4+ years in diagnostics development, including 2+ years leading CDx/IVD programs in pharma or diagnostics organizations

  • Proven delivery of CDx aligned to drug approvals, with successful validation and regulatory submissions

  • Expertise in NGS, PCR, IHC, and immunoassays, along with validation standards and quality systems

  • Strong grasp of global regulatory pathways (FDA CDRH, EU IVDR, PMDA) for CDx labeling

  • Excellent communication, leadership, and stakeholder management skills, with the ability to deliver clear updates to executive audiences

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$150,500.00 - $245,500.00

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