Principal Duties and Responsibilities: • Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry. • ...
Principal Duties and Responsibilities: • Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry. • ...
... medical device industry to every project. Our employees are important to us! We want the best for ... Formal injection molding or plastics processing certification, such as Scientific Injection Molding ...
... medical device industry to every project. Our employees are important to us! We want the best for ... Formal injection molding or plastics processing certification, such as Scientific Injection Molding ...
Process Technician
Fort Collins, CO · On-site
... medical device industry to every project. Our employees are important to us! We want the best for ... Formal injection molding or plastics processing certification, such as Scientific Injection Molding ...
Quick apply
Process Technician
Fort Collins, CO · On-site
... medical device industry to every project. Our employees are important to us! We want the best for ... Formal injection molding or plastics processing certification, such as Scientific Injection Molding ...
Process Technician
Fort Collins, CO · On-site
$25 - $40/hr
... medical device industry to every project. Our employees are important to us! We want the best for ... Formal injection molding or plastics processing certification, such as Scientific Injection Molding ...
Process Technician
Fort Collins, CO · On-site
$25 - $40/hr
... medical device industry to every project. Our employees are important to us! We want the best for ... Formal injection molding or plastics processing certification, such as Scientific Injection Molding ...
Working knowledge of medical device regulated quality or regulatory standards (FDA 21 CFR 820, ISO 13485). * Ability to recommend and implement ISO standards, testing processes, design controls, and ...
Working knowledge of medical device regulated quality or regulatory standards (FDA 21 CFR 820, ISO 13485). * Ability to recommend and implement ISO standards, testing processes, design controls, and ...
Working knowledge of medical device regulated quality or regulatory standards (FDA 21 CFR 820, ISO 13485). * Ability to recommend and implement ISO standards, testing processes, design controls, and ...
Working knowledge of medical device regulated quality or regulatory standards (FDA 21 CFR 820, ISO 13485). * Ability to recommend and implement ISO standards, testing processes, design controls, and ...
Sterile Processing Account Specialist - 61
Aurora, CO · On-site
$65K - $73K/yr
Sterile Processing Account Specialist (Hospital-Based) Denver, CO | Full-Time | Monday-Friday | $65 ... Clear pathway into the medical device industry What You'll Do * Partner daily with SPD and OR ...
Sterile Processing Account Specialist - 61
Aurora, CO · On-site
$65K - $73K/yr
Sterile Processing Account Specialist (Hospital-Based) Denver, CO | Full-Time | Monday-Friday | $65 ... Clear pathway into the medical device industry What You'll Do * Partner daily with SPD and OR ...
Sterile Processing Account Specialist (Hospital-Based) Denver, CO | Full-Time | Monday-Friday | $65 ... Clear pathway into the medical device industry What You'll Do * Partner daily with SPD and OR ...
Quick apply
Sterile Processing Account Specialist (Hospital-Based) Denver, CO | Full-Time | Monday-Friday | $65 ... Clear pathway into the medical device industry What You'll Do * Partner daily with SPD and OR ...
Medical Support Assistant
Dillon, CO · On-site
$40K - $51K/yr
Handle check-in/check-out processes * Verify patient information and eligibility * Maintain ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...
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Medical Support Assistant
Dillon, CO · On-site
$40K - $51K/yr
Handle check-in/check-out processes * Verify patient information and eligibility * Maintain ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...
Medical Support Assistant
Dillon, CO · On-site
$40K - $51K/yr
Handle check-in/check-out processes * Verify patient information and eligibility * Maintain ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...
Quick apply
Medical Support Assistant
Dillon, CO · On-site
$40K - $51K/yr
Handle check-in/check-out processes * Verify patient information and eligibility * Maintain ... Medical Device, Construction/Engineering, Government & Critical Infrastructure. Contracting ...
... processes, governance, and technology architectures needed to meet evolving regulatory obligations across pharmaceutical and medical device supply chains. * Drive AI-enabled fulfillment ...
... processes, governance, and technology architectures needed to meet evolving regulatory obligations across pharmaceutical and medical device supply chains. * Drive AI-enabled fulfillment ...
Good understanding of product development process and design control through knowledge of US FDA and international medical device regulations * Demonstrated history of successful regulatory ...
Good understanding of product development process and design control through knowledge of US FDA and international medical device regulations * Demonstrated history of successful regulatory ...
Good understanding of product development process and design control through knowledge of US FDA and international medical device regulations * Demonstrated history of successful regulatory ...
Good understanding of product development process and design control through knowledge of US FDA and international medical device regulations * Demonstrated history of successful regulatory ...
Assoc Graphic Designer
Lafayette, CO · On-site
Medical Device Manufacturing Company Location: Lafayette, CO 80026 Duration: 12 Months (Possible ... Ensure artwork follows brand guidelines, design standards, and established processes. * Proof ...
Quick apply
Assoc Graphic Designer
Lafayette, CO · On-site
Medical Device Manufacturing Company Location: Lafayette, CO 80026 Duration: 12 Months (Possible ... Ensure artwork follows brand guidelines, design standards, and established processes. * Proof ...
Assoc Graphic Designer
Lafayette, CO · On-site
Medical Device Manufacturing Company Location: Lafayette, CO 80026 Duration: 12 Months (Possible ... Ensure artwork follows brand guidelines, design standards, and established processes. * Proof ...
Assoc Graphic Designer
Lafayette, CO · On-site
Medical Device Manufacturing Company Location: Lafayette, CO 80026 Duration: 12 Months (Possible ... Ensure artwork follows brand guidelines, design standards, and established processes. * Proof ...
Sr Process Engineer
Boulder, CO · On-site
$48 - $50/hr
Medical Device Manufacturing Company Location: Boulder, CO 80301 Duration: 2 Years Shift: 1st Shift Role Summary * Support electron beam manufacturing line * Improve processes, layouts, and equipment
Quick apply
Sr Process Engineer
Boulder, CO · On-site
$48 - $50/hr
Medical Device Manufacturing Company Location: Boulder, CO 80301 Duration: 2 Years Shift: 1st Shift Role Summary * Support electron beam manufacturing line * Improve processes, layouts, and equipment
Inspector I - Non-Exempt
Louisville, CO · On-site
Medical Device Inspector Client: Medical Device Manufacturing Company Duration: 6 Months Location ... Inspect in-process and finished products per specifications * Perform visual and basic equipment ...
Inspector I - Non-Exempt
Louisville, CO · On-site
Medical Device Inspector Client: Medical Device Manufacturing Company Duration: 6 Months Location ... Inspect in-process and finished products per specifications * Perform visual and basic equipment ...
Reimbursement Consult
Lafayette, CO · On-site
S. medical device reimbursement, including regional and hospital budgets, HTA processes, and tender/supply chain processes * Experience managing complex projects and working across cross-functional ...
Reimbursement Consult
Lafayette, CO · On-site
S. medical device reimbursement, including regional and hospital budgets, HTA processes, and tender/supply chain processes * Experience managing complex projects and working across cross-functional ...
Sr. Manufacturing/Process Engineer
Westminster, CO · On-site
$109K - $141K/yr
Lead the development, validation, and continuous improvement of manufacturing and process technologies for medical device products in accordance with FDA Quality System Regulations (21 CFR Part 820 ...
Sr. Manufacturing/Process Engineer
Westminster, CO · On-site
$109K - $141K/yr
Lead the development, validation, and continuous improvement of manufacturing and process technologies for medical device products in accordance with FDA Quality System Regulations (21 CFR Part 820 ...
Sr. Manufacturing/Process Engineer
Westminster, CO · On-site
$109K - $141K/yr
Lead the development, validation, and continuous improvement of manufacturing and process technologies for medical device products in accordance with FDA Quality System Regulations (21 CFR Part 820 ...
Sr. Manufacturing/Process Engineer
Westminster, CO · On-site
$109K - $141K/yr
Lead the development, validation, and continuous improvement of manufacturing and process technologies for medical device products in accordance with FDA Quality System Regulations (21 CFR Part 820 ...
Medical Device Processing information
What is the difference between Medical Device Processing vs Medical Equipment Technician?
| Aspect | Medical Device Processing | Medical Equipment Technician |
|---|---|---|
| Certifications | Typically requires certification in sterilization or processing | Requires certification in equipment repair or biomedical technology |
| Work Environment | Cleanrooms, sterilization areas, hospitals | Hospitals, clinics, repair shops |
| Job Focus | Cleaning, sterilizing, and preparing medical devices | Maintaining, repairing, and troubleshooting medical equipment |
| Industry Usage | Hospitals, medical device companies, sterilization facilities | Hospitals, biomedical service companies |
Medical Device Processing primarily involves sterilizing and preparing devices for use, focusing on cleanliness and safety. Medical Equipment Technicians repair and maintain medical equipment. While both roles support healthcare, they differ in responsibilities, certifications, and work environments.
Is sterile processing a stressful job?
What cities in Colorado are hiring for Medical Device Processing jobs?
Cities in Colorado with the most Medical Device Processing job openings:

Full-time
Re-posted 28 days ago
Job description
Highridge Medical creates the world's most innovative spinal solutions across the spectrum from Motion Preservation to Minimally Invasive Surgery to Core Spine.
Working at Highridge Medical is not just work. Life at Highridge Medical is purpose driven. Every day, you have the privilege of using your talents to demonstrate Confidence in your work and restore Confidence for our patients. Confidence that moves.
Job Summary:
We are seeking a Project Manager to lead cross-functional teams through the full product development lifecycle, from concept through commercialization within the R&D Department. This role is responsible for project planning, schedule management, risk mitigation, and ensuring compliance with design control and quality system requirements. The NPD Project Manager will partner closely with Engineering, Marketing, Regulatory, Quality, Operations, Clinical, and Supply Chain to deliver innovative spinal implant and instrument solutions on time and within scope. Occasional travel may be required.
Principal Duties and Responsibilities:
• Leads the planning of new product development projects using structured phase-gate and design control processes common to the medical device industry.
• Develops and maintains detailed Gantt charts, project schedules, resource plans, and critical path analyses.
• Facilitates cross-functional collaboration across Engineering, Marketing, Regulatory, Quality, Operations, Clinical, Testing, and Supply Chain to ensure alignment on requirements, deliverables, and timelines.
• Leads project meetings, including kickoffs, weekly status reviews, technical reviews, and phase-gate approvals; prepares agendas, documents minutes, assigns action items, and drives accountability.
• Tracks project progress, identifies risks, and implements mitigation strategies to ensure successful execution.
• Supports the completion of project documentation that is accurate, and compliant within the Design History File (DHF).
• Supports the development and refinement of user needs, product requirements, and system specifications by coordinating input from surgeons, marketing, and engineering teams.
• Coordinates with Regulatory Affairs to ensure project deliverables support global submissions and compliance requirements.
• Works with Operations and Supply Chain to support manufacturing readiness, pilot builds, process validation, and launch planning.
• Prepares and presents project updates, dashboards, and risk assessments to leadership and executive stakeholders.
• Manages multiple concurrent projects and adjusts plans to meet evolving business priorities.
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):
Strong working knowledge of medical device product development, including design control, risk management, and quality system requirements.
• Demonstrated ability to lead cross-functional teams and influence without direct authority, consistent with practices at leading device manufacturers.
• Demonstrated creativity and ability to take actions in solving problems and making decisions in a dynamic and evolving environment.
• Proficiency in developing and managing complex project schedules, resource plans, and risk registers.
• Ability to communicate effectively with technical and non-technical stakeholders, including surgeons, engineers, executives, and external partners.
• Strong organizational skills with the ability to manage multiple high-complexity projects simultaneously.
• Experience preparing and delivering executive-level presentations and project status reports.
• Proficiency with MS Project, Smartsheet, or equivalent project management tools; strong skills in Microsoft Office Suite.
• Familiarity with manufacturing processes, design for manufacturability, and supply chain considerations for implant and instrument systems.
• Experience in a regulated medical device environment (Class II/III preferred)
Education/Experience Requirements:
• Minimum B.S. degree in Engineering, Project Management, Business, or related field.
• 3+ years of experience in project management, preferably within the medical device industry or other regulated product development environments.
• Experience managing cross-functional teams and complex product development projects.
• PMP certification or equivalent is a plus.
Please visit Highridgemedical.com for additional information.
Highridge Medical is an equal opportunity employer committed to diversity and inclusion in the workplace. All qualified applicants for employment and employment decisions are considered and evaluated without regard to race, color, religion, religious beliefs, creed, national origin, ancestry, citizenship status, age, gender, sex (including pregnancy, childbirth, related medical conditions, lactation and breastfeeding), gender identity or expression (including transgender status), sexual orientation, marital status, military status, protected veteran status, disability, protected medical condition as defined by applicable state or local law, genetic information, or any other status protected under applicable federal, state, and local laws.