ZipRecruiter

Log In

1

Senior Biomedical Manufacturing Jobs in Michigan

Stryker

Senior Staff Mechanical Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

Collaborate with Quality, Manufacturing, Regulatory Affairs, Clinical, Marketing, and Project ... Bachelor of Science degree in Engineering, Mechanical Engineering, Biomedical Engineering, or a ...

Stryker

Senior Staff Mechanical Engineer, R&D

Portage, MI · On-site

$102K - $171K/yr

Collaborate with Quality, Manufacturing, Regulatory Affairs, Clinical, Marketing, and Project ... Bachelor of Science degree in Engineering, Mechanical Engineering, Biomedical Engineering, or a ...

next page

Showing results 1-20

All JobsBiomedical Manufacturing JobsSenior Biomedical Manufacturing JobsSenior Biomedical Manufacturing Jobs in Michigan

Senior Biomedical Manufacturing information

What is the difference between Senior Biomedical Manufacturing vs Biomedical Manufacturing Technician?

AspectSenior Biomedical ManufacturingBiomedical Manufacturing Technician
CredentialsBachelor's degree, certifications in GMP, ISO, or quality assuranceAssociate's degree or technical certification, on-the-job training
Work EnvironmentManufacturing facilities, quality control labs, R&D settingsProduction floors, assembly lines, equipment setup
Employer & Industry UsageBiotech firms, medical device companies, pharmaceutical manufacturersMedical device manufacturing plants, biotech companies

The main difference between Senior Biomedical Manufacturing and Biomedical Manufacturing Technician lies in experience, responsibilities, and qualifications. Senior roles typically involve overseeing production processes, quality assurance, and team leadership, requiring more advanced education and experience. Technicians focus on hands-on manufacturing, equipment operation, and assembly, often with technical certifications. Both roles are essential in the biomedical industry, but they differ in scope and seniority.

What is senior biomedical manufacturing?

Senior biomedical manufacturing involves overseeing the production of medical devices, equipment, or pharmaceuticals, ensuring quality control, compliance with regulations, and efficient processes. Professionals in this role often require knowledge of manufacturing protocols, regulatory standards like FDA or ISO, and may lead teams or projects within a biomedical production environment.

What are popular job titles related to Senior Biomedical Manufacturing jobs in Michigan?

For Senior Biomedical Manufacturing jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Senior Biomedical Manufacturing jobs in Michigan look for?

The top searched job categories for Senior Biomedical Manufacturing jobs in Michigan are:

What cities in Michigan are hiring for Senior Biomedical Manufacturing jobs?

Cities in Michigan with the most Senior Biomedical Manufacturing job openings:

Senior Biomedical Manufacturing jobs near you
Infographic showing various Senior Biomedical Manufacturing job openings in Michigan as of August 2026, with employment types broken down into 88% Full Time, 4% Part Time, 1% Temporary, 4% Contract, and 3% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Senior Staff Mechanical Engineer, R&D

Stryker Group

Portage, MI • On-site

$103 - $171/hr

Other

Posted 21 days ago

Job description

Senior Staff Mechanical Engineer Lead, R&D

Portage, MI

Join a team focused on advancing complex medical technologies through engineering excellence and cross-functional collaboration. This role offers the opportunity to lead technical development efforts, contribute to innovation initiatives, and apply advanced engineering expertise across the full product development lifecycle. The Senior Staff R&D Engineer Lead serves as a technical leader, guiding design decisions, mentoring engineers, and supporting the development of compliant, high-quality products.

Work Flexibility:

Hybrid: candidates must reside within commuting distance of Portage, MI and be able to work onsite several days per week.

What You Will Do
  • Lead the research, design, development, modification, and evaluation of complex modules, assemblies, and subsystems throughout the product development lifecycle.
  • Translate user needs into engineering requirements, specifications, and system-level designs, ensuring alignment with product and business objectives.
  • Design and execute advanced prototyping and testing activities to verify product performance and design requirements.
  • Resolve complex product design challenges and drive implementation of corrective actions to support product readiness and quality standards.
  • Explore emerging technologies and recommend applications that support product innovation and business needs.
  • Develop invention disclosures, patents, and trade secret documentation to support intellectual property initiatives.
  • Collaborate with Quality, Manufacturing, Regulatory Affairs, Clinical, Marketing, and Project Management teams to deliver projects according to business and development milestones.
  • Mentor engineers on engineering principles, design controls, industry standards, engineering documentation, and technical best practices.
What You Will NeedRequired Qualifications
  • Bachelor of Science degree in Engineering, Mechanical Engineering, Biomedical Engineering, or a related engineering discipline.
  • Minimum 6 years of engineering experience in Research & Development (R&D)
  • Experience creating engineering drawings, technical documentation, and 3D models.
  • Proficiency with PTC Creo for 3D modeling and engineering design.
Preferred Qualifications
  • Experience developing and optimizing complex mechanical and/or electro-mechanical assemblies using Design for Manufacturability (DFM) principles.
  • Experience applying Geometric Dimensioning and Tolerancing (GD&T) in engineering drawings.
  • Experience using Computer-Aided Engineering (CAE) tools to evaluate and optimize product designs.
  • Knowledge of materials, manufacturing processes, and processing technologies used in complex product development.
  • Experience supporting medical device development within a regulated environment.

$102,600 - $171,000 USD Annual

#J-18808-Ljbffr

Apply