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Master Biomedical Engineering Jobs in Michigan (NOW HIRING)

Manager, Process Development

Brighton, MI ยท On-site

$100K - $120K/yr

Develop, review, and maintain Master Batch Records, Standard Operating Procedures (SOPs ... What You Bring * Bachelor's degree in Biology, Chemistry, Chemical Engineering, Biomedical ...

Develop, review, and maintain Master Batch Records, Standard Operating Procedures (SOPs ... What You Bring * Bachelor's degree in Biology, Chemistry, Chemical Engineering, Biomedical ...

Manager, Process Development

Brighton, MI ยท On-site

$100K - $120K/yr

Develop, review, and maintain Master Batch Records, Standard Operating Procedures (SOPs ... What You BringBachelor's degree in Biology, Chemistry, Chemical Engineering, Biomedical Engineering ...

Senior Quality Engineer

Clinton, MI ยท On-site

$87K - $118K/yr

Develop, and review IQ/OQ/PQ ValidationProtocols, Summary Reports, Validation Master Plans for ... Bachelor's degree in Biomedical Engineering, or Aerospace Engineering, or Mechanical Engineering ...

Data Architect Senior

Ann Arbor, MI ยท On-site

$65.75 - $88/hr

Master's degree or higher in computer science, data science, computer engineering, biomedical engineering, bioinformatics, informatics, or a related field. Candidates with substantial equivalent ...

PrincipalVehicle Safety Engineer

Troy, MI ยท On-site

$123K - $185K/yr

Bachelor's degree in mechanical, Automotive, or Biomedical Engineering (Master's preferred) * 10+ years of direct automotive experience in vehicle safety, crash testing, or restraint system ...

Principal Vehicle Safety Engineer

Troy, MI ยท On-site

$123 - $185/hr

Bachelor's degree in mechanical, Automotive, or Biomedical Engineering (Master's preferred) * 10+ years of direct automotive experience in vehicle safety, crash testing, or restraint system ...

Principal Vehicle Safety Engineer

Troy, MI ยท On-site

$123K - $185K/yr

Bachelor's degree in mechanical, Automotive, or Biomedical Engineering (Master's preferred) * 10+ years of direct automotive experience in vehicle safety, crash testing, or restraint system ...

A bachelor's degree in Aerospace/Aeronautical, Biomedical/Biomechanical/Bioengineering, Chemical ... Master's degree in engineering or a master's in business administration * Green Belt or Black Belt ...

A bachelor's degree in Aerospace/Aeronautical, Biomedical/Biomechanical/Bioengineering, Chemical ... Master's degree in engineering or a master's in business administration * Green Belt or Black Belt ...

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Showing results 1-20

Master Biomedical Engineering information

See Michigan salary details

$35.7K

$82.6K

$122K

How much do master biomedical engineering jobs pay per year?

As of Aug 22, 2026, the average yearly pay for master biomedical engineering in Michigan is $82,633.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,900.00 and $101,100.00 per year, depending on experience, location, and employer.

What is a master in biomedical engineering?

A Master in Biomedical Engineering is a graduate-level degree that combines principles of engineering, biology, and medicine to develop technologies and devices that improve healthcare. The program typically includes advanced coursework in areas such as biomechanics, medical imaging, biomaterials, and bioinformatics. Graduates are trained to design and create medical devices, develop new therapies, and work on innovative healthcare solutions. This degree prepares students for careers in medical device industries, research institutions, hospitals, or further doctoral studies.

What are some typical interdisciplinary collaborations for a master biomedical engineer?

Professionals in a Master Biomedical Engineering role frequently collaborate with experts from diverse fields such as medicine, biology, materials science, and computer science. These interdisciplinary teams work together to develop innovative medical devices, diagnostic tools, and therapeutic solutions. Regular interaction with clinicians provides valuable feedback on device usability, while cooperation with regulatory specialists ensures compliance with industry standards. Such collaborations not only enhance project outcomes but also offer opportunities for skill development and career growth.

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

To thrive as a Master Biomedical Engineer, you need a strong background in biology, engineering principles, and mathematics, typically supported by a master's degree in biomedical engineering or a related field. Proficiency in CAD software, programming languages (such as MATLAB or Python), and an understanding of regulatory standards (like FDA or ISO) are commonly required. Excellent problem-solving skills, teamwork, and effective communication set outstanding professionals apart in this role. These skills are crucial for developing safe, innovative medical devices and technologies that improve patient care and meet industry regulations.

What is the difference between Master Biomedical Engineering vs Biomedical Engineer?

AspectMaster Biomedical EngineeringBiomedical Engineer
Required CredentialsMaster's degree in biomedical engineering or related fieldBachelor's degree in biomedical engineering or related field
Work EnvironmentResearch labs, hospitals, medical device companiesHospitals, medical device firms, research institutions
Industry UsageDesign, research, advanced developmentImplementation, testing, maintenance of medical devices

The Master Biomedical Engineering typically involves advanced coursework and research, preparing professionals for specialized roles or further study. Biomedical Engineers focus on applying engineering principles to develop and maintain medical devices and systems. Both roles are essential in the healthcare industry, but the master's level emphasizes research and design, while the bachelor's level emphasizes practical application and implementation.

Is a master's in biomedical engineering worth it?

A master's in biomedical engineering can enhance job prospects, leading to roles in medical device design, research, and development. It often increases earning potential and provides specialized skills in areas like biomaterials, imaging, and regulatory compliance, making it a valuable credential for advancing in the field.

What can I do with a master's in biomedical engineering?

A master's in biomedical engineering prepares individuals for roles such as biomedical engineer, research scientist, or clinical engineer, involving the design and development of medical devices, equipment, and technologies. Graduates often work in healthcare, research institutions, or industry settings, utilizing skills in engineering, biology, and computer science, and may pursue certifications or advanced training for specialized positions.

What are popular job titles related to Master Biomedical Engineering jobs in Michigan?

For Master Biomedical Engineering jobs in Michigan, the most frequently searched job titles are:

Infographic showing various Master Biomedical Engineering job openings in Michigan as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $82,633 per year, or $39.7 per hour.

Manager, Process Development

Biovire

Brighton, MI โ€ข On-site

$100K - $120K/yr

Full-time

Medical, Dental, Vision, Life, PTO

Posted 24 days ago


Job description

Manager, Process Development
Engineering Organization
Brighton, Michigan
Biovire is advancing toward commercialization with a focus on innovation, operational excellence, and scalable GMP manufacturing. We are seeking a Manager, Process Development to lead technical transfer activities for sterile injectable pharmaceutical and medical device products while driving process robustness, manufacturing readiness, and continuous improvement across our Brighton manufacturing facility.
This is a highly visible leadership role responsible for leading Process Development activities that support new product introductions, technology transfer, process optimization, and successful commercialization while partnering closely with Manufacturing, Quality, Validation, Engineering, and other cross-functional teams.
The Role
Reporting to the Director, Pharmaceutical Technologies, the Manager, Process Development, provides technical and people leadership for product transfer and process development activities that support sterile injectable pharmaceutical and medical device manufacturing.
This role leads a team of Process Engineers and ensures that manufacturing processes are technically sound, scalable, compliant, and capable of consistently producing high-quality products. The position partners closely with Manufacturing, Quality, Validation, Engineering, Supply Chain, and other cross-functional stakeholders to support successful product launches, operational readiness, and continuous process improvement.
Key Responsibilities
  • Lead technical transfer activities for sterile injectable pharmaceutical and medical device products from development through commercial manufacturing.
  • Manage and develop a team of Process Engineers while fostering a collaborative, high-performing culture.
  • Partner with Manufacturing to support production schedules and ensure successful execution of product transfer activities.
  • Drive process optimization, continuous improvement, and implementation of manufacturing best practices.
  • Ensure compliance with current Good Manufacturing Practices (cGMP), company policies, quality standards, and regulatory requirements.
  • Develop, review, and maintain Master Batch Records, Standard Operating Procedures (SOPs), validation master plans, cleaning validation documentation, containment strategies, and technical transfer documentation.
  • Utilize manufacturing expertise to identify opportunities for process improvements that enhance product quality, efficiency, and operational reliability.
  • Collaborate cross-functionally with Manufacturing, Quality, Validation, Engineering, and other operational teams to ensure successful product transfers and commercialization.
  • Support manufacturing investigations, technical problem-solving, and implementation of corrective and preventive actions as appropriate.
  • Lead training, coaching, and development of Process Engineers while promoting accountability, technical excellence, and continuous learning.
  • Promote a safe working environment and reinforce Biovire's commitment to quality, compliance, and operational excellence.

What You Bring
  • Bachelor's degree in Biology, Chemistry, Chemical Engineering, Biomedical Engineering, or another related life science or technical discipline required.
  • Graduate degree in Chemistry, Biochemistry, Molecular Biology, Chemical Engineering, Biomedical Engineering, or a related life science preferred.
  • Minimum 5 years of pharmaceutical industry experience.
  • 2-5 years of leadership or people management experience preferred.
  • Demonstrated experience supporting process development, technical transfer, or pharmaceutical manufacturing operations.
  • Strong understanding of cGMP requirements, pharmaceutical manufacturing processes, and regulatory expectations.
  • Experience developing or maintaining manufacturing documentation including Master Batch Records, SOPs, validation documentation, and technical transfer packages.
  • Excellent organizational, communication, technical writing, and cross-functional collaboration skills.
  • Proven ability to lead teams, prioritize multiple projects, and drive continuous improvement initiatives.
  • Demonstrated commitment to safety, quality, integrity, and operational excellence.

Why Join Biovire
  • Opportunity to lead technical transfer and process development activities supporting commercialization of innovative therapies.
  • High visibility and cross-functional leadership exposure across Manufacturing, Engineering, Quality, Validation, and Pharmaceutical Technologies.
  • Collaborative and mission-driven GMP manufacturing environment.
  • Direct impact on new product introductions, manufacturing readiness, and continuous improvement initiatives.
  • Company-sponsored medical, dental, vision, and life insurance.
  • Paid Time Off supporting work-life balance.
  • Opportunity to build and develop a growing Process Development team.

Come join us on our mission of manufacturing safe, high-quality products that improve and save lives.