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Biomedical Engineer Manager Jobs in Colorado (NOW HIRING)

Leads the creation of project plans and manages critical project timelines. * Leads the development ... Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering ...

Leads the creation of project plans and manages critical project timelines. * Leads the development ... Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering ...

Biomedical Equipment Tech Sr

Longmont, CO · On-site

$37.40 - $55.57/hr

LPH Clinical Engineering Work Schedule: Full Time, 80.00 hours per pay period (2 weeks) Shift: Days ... Promptly escalates issues to higher level technical support or management when necessary. Performs ...

Clinical Engineering Work Schedule: Full Time, 80.00 hours per pay period (2 weeks) Shift: Days Pay ... Promptly escalates issues to higher level technical support or management when necessary. Performs ...

Clinical Engineering Work Schedule: Full Time, 80.00 hours per pay period (2 weeks) Shift: Days Pay ... Promptly escalates issues to higher level technical support or management when necessary. Performs ...

LPH Clinical Engineering Work Schedule: Full Time, 80.00 hours per pay period (2 weeks) Shift: Days ... Promptly escalates issues to higher level technical support or management when necessary. Performs ...

Aerospace Engineering, Automotive Engineering, Biomedical Engineering, Chemical Engineering ... management software - Excelling in strategic sourcing and procurement processes - Utilizing ...

PD Program Manager

Lafayette, CO · On-site

$163K - $204K/yr

PD Program Manager for Medtronic, Inc. Lead released product management (RPM)/sustainment programs ... Bachelor's degree in Mechanical Engineering, Industrial Engineering or Biomedical Engineering or ...

PD Program Manager for Medtronic, Inc. Lead released product management (RPM)/sustainment programs ... Bachelor's degree in Mechanical Engineering, Industrial Engineering or Biomedical Engineering or ...

PD Program Manager

Lafayette, CO · On-site

$163K - $204K/yr

PD Program Manager for Medtronic, Inc. Lead released product management (RPM)/sustainment programs ... Bachelor's degree in Mechanical Engineering, Industrial Engineering or Biomedical Engineering or ...

Senior Quality Engineer

Englewood, CO · On-site

$110K - $125K/yr

Bachelor's degree in Biomedical Engineering, Quality Management, or a related technical field. * 5+ years of experience in quality engineering or quality assurance roles within a manufacturing or ...

Apply applicable regulations and standards to design controls, risk management, and product ... Bachelor's degree in Mechanical Engineering, Materials Engineering, Biomedical Engineering, or ...

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Biomedical Engineer Manager information

See Colorado salary details

$43.1K

$99.7K

$147.2K

How much do biomedical engineer manager jobs pay per year?

As of Jun 13, 2026, the average yearly pay for biomedical engineer manager in Colorado is $99,691.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,300.00 and $122,000.00 per year, depending on experience, location, and employer.

What does a Biomedical Engineer Manager do?

A Biomedical Engineer Manager oversees the design, development, and maintenance of medical equipment and healthcare technology. They lead teams of biomedical engineers, ensuring compliance with industry regulations and safety standards. Their responsibilities include project management, budgeting, vendor coordination, and collaboration with healthcare professionals to improve medical device performance. Additionally, they may conduct research to innovate new technologies and optimize existing systems. Effective communication and leadership skills are essential for managing both technical and organizational aspects of the role.

What are the typical daily responsibilities of a Biomedical Engineer Manager?

A Biomedical Engineer Manager’s day often involves overseeing engineering teams, guiding medical device development projects, and ensuring product compliance with healthcare regulations. They regularly coordinate with cross-functional groups, including research scientists, clinicians, and regulatory specialists, to align project objectives and timelines. Managers also allocate resources, address technical and personnel challenges, and provide mentoring to junior engineers. This role requires balancing hands-on technical work with strategic planning to deliver safe, effective medical solutions on time and within budget.

What are the key skills and qualifications needed to thrive in the Biomedical Engineer Manager position, and why are they important?

To thrive as a Biomedical Engineer Manager, you need a strong background in biomedical engineering, project management experience, and often a relevant bachelor's or master's degree. Familiarity with regulatory compliance systems (such as FDA standards), medical device development tools, and quality assurance certifications like PMP or Six Sigma is highly valued. Outstanding interpersonal communication, leadership, and problem-solving skills help distinguish top performers in this role. These skills ensure successful project delivery, regulatory compliance, and effective team leadership in a complex, multidisciplinary environment.

What are the most commonly searched types of Biomedical Engineer jobs in Colorado? The most popular types of Biomedical Engineer jobs in Colorado are:
What cities in Colorado are hiring for Biomedical Engineer Manager jobs? Cities in Colorado with the most Biomedical Engineer Manager job openings:

Sr Development Engineer I

Highridge Medical

Westminster, CO • On-site

$83K - $100K/yr

Full-time

Posted 8 days ago


Job description

Sr Development Engineer I
Principal Duties and Responsibilities:
• Contributes to the design and development of new products and improvements to existing products from conception to launch following Design Control procedures.
• Develops project plans and manages critical project timelines.
• Develops innovative solutions in a team environment to address clinical problems and translates ideas into concepts, functional prototypes and ultimately a commercialized product.
• Collects surgeon feedback and defines user needs, specifications, and performance criteria.
• Generates CAD models and engineering drawings primarily within SolidWorks.
• Authors and maintains design control documentation within a DHF.
• Supports test strategy development and contributes to test protocol/report creation.
• Defines and executes verification and validation activities with support from testing and quality teams.
• Designs components for manufacturability, inspectability, and cost-effectiveness.
• Participates in root cause investigations and corrective actions.
• Contributes to generation of comprehensive protocols and reports for ASTM and non-standard testing or evaluation of products.
• Contributes to invention disclosures and IP generation.
This is not an exhaustive list of duties or functions and may not necessarily comprise all of the "essential functions" for purposes of the ADA.
Expected Areas of Competence (i.e., knowledge, skills, and abilities)
• Full working knowledge of and moderate level of experience with new product development, including familiarity with design control processes.
• Demonstrated ability to methodically investigate technical issues, identify appropriate solutions, and apply current technologies to resolve problems.
• Ability to develop and maintain project schedules and track cross-functional team progress to meet deadlines.
• Ability to identify customer complaints, process engineering change requests, address nonconforming product, and provide sound technical recommendations.
• Professional, concise, and tactful in communications with internal teams and external stakeholders, including surgeons and suppliers.
• Effectively communicates with internal personnel, external customers, and vendors to accomplish project objectives.
• Effective written and verbal communication skills, including the ability to create and deliver technical presentations.
• Working knowledge of drafting standards and geometric dimensioning and tolerancing (GD&T).
• Familiarity with and ability to support Quality Assurance and Regulatory requirements applicable to the medical device industry.
• Ability to manage multiple projects at one time throughout all stages of the development process.
• Proficient in CAD design and engineering drawings, preferably using SolidWorks.
• Proficient with Microsoft Office Suite and MS Project.
Education/Experience Requirements
• Minimum B.S. degree from an ABET accredited school (or global equivalent) in one of the following engineering disciplines: Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering, Biomedical Engineering Technology, Bioengineering Technology, Aerospace Engineering or Aeronautical Engineering.
• 3-7 years of experience in the Medical device industry, particularly in orthopaedic devices.
Travel Requirements
Up to 10%
Salary Range $83,000.00- 100,000.00