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Biomedical Project Manager Jobs in Colorado (NOW HIRING)

Highridge Medical

Sr Development Engineer I

Westminster, CO · On-site

$83K - $100K/yr

... plans and manages critical project timelines. • Develops innovative solutions in a team ... Mechanical Engineering, Mechanical Engineering Technology, Biomedical Engineering, Bioengineering ...

Highridge Medical

Dev Principal Engineer

Westminster, CO · On-site

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

Highridge Medical

Dev Principal Engineer

Westminster, CO · On-site

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

MM Solutions

Design & Engineering Manager

Loveland, CO · On-site

$90K - $130K/yr

Design custom packaging and transportation solutions for various industries including biomedical ... Generate project estimates and develop quotes in Salesforce. Present prototypes and designs to ...

Excelitas Technologies

Senior Buyer

Boulder, CO

... biomedical, semiconductor, industrial, consumer products, scientific, security, defense and ... Main responsibilities: * Works closely and collaboratively with Project Managers, Engineers ...

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All JobsBiomedical Project Manager JobsBiomedical Project Manager Jobs in Colorado

Biomedical Project Manager information

See Colorado salary details

$23

$48

$80

How much do biomedical project manager jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for biomedical project manager in Colorado is $48.62, according to ZipRecruiter salary data. Most workers in this role earn between $42.21 and $53.32 per hour, depending on experience, location, and employer.

What is the highest paying project manager job?

In the biomedical field, senior-level project managers with extensive experience, advanced certifications like PMP, and specialized knowledge in areas such as clinical trials or regulatory compliance tend to have the highest salaries. Roles overseeing large, complex projects or managing multiple teams often offer higher compensation, especially in pharmaceutical or biotech companies.

What is the difference between Biomedical Project Manager vs Biomedical Engineer?

AspectBiomedical Project ManagerBiomedical Engineer
Required CredentialsBachelor's or Master's in Biomedical Engineering, Project Management CertificationBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentProject teams, clinical settings, R&D departmentsLaboratories, manufacturing, clinical research
Employer & Industry UsageHospitals, biotech firms, medical device companiesMedical device companies, research institutions, hospitals

The Biomedical Project Manager focuses on overseeing projects, coordinating teams, and ensuring timely delivery of biomedical products. In contrast, the Biomedical Engineer is involved in designing, developing, and testing medical devices or systems. While both roles require biomedical engineering knowledge, the project manager emphasizes management skills and project execution, whereas the engineer concentrates on technical development and innovation.

What is the highest paying biomedical job?

The highest paying biomedical jobs are often executive roles such as Chief Medical Officer or Vice President of Research, which can earn six-figure salaries. Senior roles in biotech or pharmaceutical companies that involve strategic leadership, extensive experience, and advanced degrees tend to have the highest compensation in the biomedical field.

What are Biomedical Project Managers?

Biomedical Project Managers are professionals responsible for overseeing and coordinating biomedical research projects, clinical trials, or product development within the healthcare or life sciences industry. They ensure that projects are completed on time, within budget, and in compliance with regulatory standards. Their role involves managing teams, communicating with stakeholders, and addressing potential risks or issues during the project lifecycle. Biomedical Project Managers often work closely with scientists, engineers, medical staff, and regulatory bodies to facilitate successful project outcomes.

What do Project Managers do in biotech?

Biotech project managers oversee the planning, execution, and completion of research and development projects, ensuring they meet deadlines, budgets, and regulatory standards. They coordinate teams, manage resources, and communicate progress to stakeholders, often using project management tools like Gantt charts and tracking software. Strong organizational, communication, and industry-specific knowledge are essential for success in this role.

How does a Biomedical Project Manager typically collaborate with cross-functional teams during a project lifecycle?

A Biomedical Project Manager works closely with diverse teams such as research scientists, regulatory specialists, engineers, and clinical staff to ensure project milestones are met. They facilitate communication across these groups by organizing regular meetings, tracking progress, and resolving issues that arise. This collaborative approach helps align project objectives, address challenges promptly, and maintain compliance with regulatory standards. Effective coordination and relationship-building are key to successfully delivering complex biomedical projects on time and within budget.

What is the role of a biomedical manager?

A biomedical project manager oversees the planning, execution, and completion of biomedical projects, ensuring compliance with regulatory standards and managing cross-disciplinary teams. They coordinate activities related to medical device development, testing, and implementation, often utilizing project management tools and certifications such as PMP or CAPM. Their role involves ensuring projects meet technical specifications, budgets, and deadlines in healthcare or research environments.

What are the key skills and qualifications needed to thrive as a Biomedical Project Manager, and why are they important?

To thrive as a Biomedical Project Manager, you need a solid background in biomedical sciences or engineering, project management experience, and often a relevant degree such as a BS/MS in a related field. Familiarity with project management software (e.g., MS Project, Asana), regulatory compliance systems (like FDA or ISO standards), and sometimes a PMP certification are typically important. Outstanding communication, leadership, and problem-solving skills help you coordinate cross-functional teams and manage stakeholder expectations. These competencies ensure successful project delivery, regulatory compliance, and effective collaboration in the complex biomedical industry.
What are popular job titles related to Biomedical Project Manager jobs in Colorado? For Biomedical Project Manager jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Biomedical Project Manager jobs in Colorado look for? The top searched job categories for Biomedical Project Manager jobs in Colorado are:
What cities in Colorado are hiring for Biomedical Project Manager jobs? Cities in Colorado with the most Biomedical Project Manager job openings:
Biomedical Project Manager jobs near you

Sr Development Engineer I

Highridge Medical

Westminster, CO

$83K - $100K/yr

Full-time

Posted 10 hours 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

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