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Highridge Medical

S&OP Supply Manager

Westminster, CO · On-site

S&OP Supply Manager Essential Duties & Responsibilities: S&OP Process Ownership Own the supply planning cycle within the monthly S&OP process Drive alignment to a consensus supply plan signed off at ...

Highridge Medical

Project Manager

Westminster, CO · On-site

Project Manager Note: This is a part-time in office position based out of Westminster Colorado. Principal Duties and Responsibilities: * Be the process expert by being responsible for incorporating ...

Highridge Medical

Industrial Engineer

Olive Branch, MS · On-site

$62K - $84K/yr

Industrial Engineer Job Summary: The Industrial Engineer will lead and manage challenging cross-functional projects to deliver exceptional customer service world class and distribution performance.

Highridge Medical

Warehouse Coordinator

Olive Branch, MS · On-site

$16.25 - $20.75/hr

Warehouse Coordinator Principal Duties and Responsibilities * Monitors orders created in SAP and releases for processing. * Performs work functions to assist department in accomplishing daily goals ...

Highridge Medical

Project Manager

Westminster, CO · On-site

Project Manager Note: This is a part-time in office position based out of Westminster Colorado. Principal Duties and Responsibilities: * Be the process expert by being responsible for incorporating ...

Highridge Medical

QMS Specialist

Westminster, CO · On-site

QMS Specialist Principal Duties and Responsibilities Material Documentation Support and Testing Implement and maintain the CAPA program including software solutions. Duties include, but are not ...

Highridge Medical

Industrial Engineer

Olive Branch, MS · On-site

$62K - $84K/yr

Industrial Engineer Job Summary: The Industrial Engineer will lead and manage challenging cross-functional projects to deliver exceptional customer service world class and distribution performance.

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What is the difference between Highridge vs Geotechnical Engineer?

AspectHighridgeGeotechnical Engineer
Required CredentialsBachelor's degree in environmental science, geology, or related field; certifications varyBachelor's or master's in geotechnical engineering or geology; licensure often required
Work EnvironmentFieldwork, environmental consulting sites, laboratoriesSite investigations, design projects, consulting firms
Employer & Industry UsageEnvironmental consulting firms, government agenciesEngineering consulting firms, construction, infrastructure projects
Common Search & ComparisonHighridge vs Geotechnical Engineer

Highridge professionals typically focus on environmental assessments and remediation, often working in environmental consulting and fieldwork. Geotechnical Engineers specialize in soil and foundation analysis for construction projects. While both roles require related degrees and involve site work, their primary focus and industry applications differ, making this comparison useful for those exploring careers or hiring in these fields.

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Infographic showing various Highridge job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 75% In-person, and 25% Hybrid job distribution.

Sr Development Engineer I

Highridge Medical

Westminster, CO • On-site

$83K - $100K/yr

Full-time

Re-posted 9 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

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