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Medical Device Manufacturing Jobs in Highlands Ranch, CO

LivaNova PLC

Quality Engineer

Arvada, CO · On-site

$85 - $95/hr

... medical device manufacturing and distribution. The role evaluates non‑conforming products, analyzes data, proposes product disposition, initiates CAPAs, and communicates findings to manufacturers ...

Cobioscience

Training Manager

Arvada, CO · On-site

$95 - $125/hr

Experience supporting medical device, pharmaceutical, biotech, aerospace, or similarly regulated manufacturing organizations. * Experience creating and managing skills matrices, qualification systems ...

New

LivaNova

Training Manager

Arvada, CO · On-site

$95K - $125K/yr

Experience in medical device manufacturing. * Knowledge of FDA Quality System Regulations, ISO 13485, GMP, and Good Documentation Practices. * Experience implementing Learning Management Systems (LMS)

LivaNova, PLC

Training Manager

Arvada, CO · On-site

$95K - $125K/yr

Experience in medical device manufacturing. * Knowledge of FDA Quality System Regulations, ISO 13485, GMP, and Good Documentation Practices. * Experience implementing Learning Management Systems (LMS)

LivaNova PLC

Quality Engineer (On-site)

Arvada, CO · On-site

$67.50 - $82.50/hr

... medical device manufacturing and distribution. He/she evaluates situations of non‑conforming products, collects and analyzes data to propose product disposition and CAPA's to address quality issues.

LivaNova

Quality Engineer

Arvada, CO · On-site

$85K - $95K/yr

Minimum related work experience of 1-3 years in Class II/III medical device manufacturing or related regulatory industry. Knowledge of regulatory requirements (e.g., FDA, ISO 13485) as required for ...

LivaNova

Quality Engineer (On-site)

Denver, CO · On-site

$74K - $95K/yr

... medical device manufacturing and distribution. He/she evaluates situations of non-conforming products, collects and analyses data to propose product disposition and CAPA's to address quality issues.

LivaNova, PLC

Quality Engineer

Arvada, CO · On-site

$85K - $95K/yr

... medical device manufacturing and distribution. Evaluates situations of non-conforming products, collects and analyses data to propose product disposition and CAPA's to address quality issues. This ...

LivaNova, PLC

Quality Engineer (On-site)

Denver, CO · On-site

$74K - $95K/yr

... medical device manufacturing and distribution. He/she evaluates situations of non-conforming products, collects and analyses data to propose product disposition and CAPA's to address quality issues.

Actalent

Electrical Engineer

Highlands Ranch, CO

$120K - $160K/yr

Work Environment You will work in a small, highly collaborative engineering team in a regulated medical device manufacturing environment. The role is fully onsite, five days per week, providing ...

Actalent

Electrical Engineer

Highlands Ranch, CO

$120K - $160K/yr

Work Environment You will work in a small, highly collaborative engineering team in a regulated medical device manufacturing environment. The role is fully onsite, five days per week, providing ...

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Showing results 21-40

All JobsMedical Device Manufacturing JobsMedical Device Manufacturing Jobs in Highlands Ranch, CO

Medical Device Manufacturing information

See Highlands Ranch, CO salary details

$19

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$42

How much do medical device manufacturing jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for medical device manufacturing in Highlands Ranch, CO is $28.47, according to ZipRecruiter salary data. Most workers in this role earn between $24.23 and $33.32 per hour, depending on experience, location, and employer.

What is a medical device manufacturing job?

A Medical Device Manufacturing job involves producing, assembling, and testing medical devices to ensure they meet regulatory and quality standards. Workers in this field may operate machinery, inspect products, and follow strict guidelines to maintain safety and efficiency. Roles can range from machine operators and quality control inspectors to engineers and regulatory compliance specialists. This industry is essential for creating devices like surgical instruments, pacemakers, and diagnostic equipment used in healthcare. Attention to detail, adherence to regulations, and technical skills are key for success in this field.

What are the key skills and qualifications needed to thrive in medical device manufacturing?

To thrive in Medical Device Manufacturing, you need strong attention to detail, knowledge of quality assurance processes, and an understanding of regulatory standards such as ISO 13485 or FDA requirements. Experience with manufacturing equipment, ERP systems, and specialized tools for assembly and testing is typically required, and certification in areas like Six Sigma or Lean Manufacturing can be advantageous. Effective communication, teamwork, and problem-solving skills help individuals excel in fast-paced, multidisciplinary environments. These skills are vital for maintaining product safety, ensuring regulatory compliance, and meeting production targets in the highly regulated medical device industry.

What career advancement opportunities are available in medical device manufacturing?

Medical Device Manufacturing offers a variety of career advancement paths, allowing employees to move into roles such as production supervisor, quality assurance specialist, or process engineer as they gain experience. Many companies provide on-the-job training, mentorship programs, and support for additional certifications to help employees further develop their technical and leadership skills. Team members who demonstrate strong performance and a commitment to continuous improvement may also transition into management positions or cross-functional roles in research and development, regulatory affairs, or supply chain management. This field values both specialized technical expertise and a proactive approach to professional growth, providing long-term career stability and diverse opportunities.

Is medical device manufacturing a good career?

Medical device manufacturing is a stable career that involves assembling, testing, and quality control of medical equipment, often requiring technical skills and certifications. It offers opportunities for advancement and typically provides a clean, regulated work environment, with demand driven by healthcare industry growth.

What cities near Highlands Ranch, CO are hiring for Medical Device Manufacturing jobs?

Cities near Highlands Ranch, CO with the most Medical Device Manufacturing job openings:

Medical Device Manufacturing jobs near you
Infographic showing various Medical Device Manufacturing job openings in Highlands Ranch, CO as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $59,210 per year, or $28.5 per hour.

Quality Engineer

LivaNova PLC

Arvada, CO • On-site

$85 - $95/hr

Other

Re-posted 3 days ago

Job description

Position Summary

With a high degree of autonomy, the Quality Engineer will contribute to ensuring that production and process control activities are conducted in compliance with the company quality management system and the international regulations governing medical device manufacturing and distribution. The role evaluates non‑conforming products, analyzes data, proposes product disposition, initiates CAPAs, and communicates findings to manufacturers or develops process improvements.

Responsibilities
  • Support Quality Management for executing quality engineering activities related to design and manufacture of products in compliance with the Quality Management System requirements and applicable regulations.
  • Collect and critically analyze data and take disposition decisions on non‑conforming products identified in production.
  • Lead proper investigations to identify causes of component/product failures (nonconforming products from production and complaints).
  • Generate risk evaluations for nonconforming products already distributed (Health Hazard Evaluation) to assist management in determining whether to stop shipment or initiate field action.
  • Lead CAPA projects and trend data to identify opportunities for future CAPAs.
  • Support external manufacturers of semi‑finished and finished products in managing any detected nonconformities, notifying suppliers of non‑conformance related to purchased material, and evaluating corrective action consistency versus internal controls.
  • Establish product quality control inspection plans, review process validation planning, protocols, and reports.
  • Preliminary review of change impact assessment to confirm quality requirements are met.
  • Maintain Risk Management files and collaborate in investigations into the causes of V&V failures.
  • Identify opportunities for quality improvements in the production area and lead improvement plans.
  • Daily management of assigned complaint handling activities related to customer use of the device, evaluating and investigating complaints, and providing timely analysis to meet Customer Quality complaint and MDR reporting quality metrics.
  • Lead effective meetings, conduct presentations, and establish quality records to support resolution of customer complaints.
  • Develop effective relationships with internal personnel and external stakeholders to assist customers.
Qualifications
  • 1‑3 years of related experience in Class II/III medical device manufacturing or related regulatory industry.
  • Knowledge of regulatory requirements (e.g., FDA, ISO13485).
  • Experience with MDSAP and Medical Device Requirements is a plus.
  • Proficiency with quality tools such as flowcharts, statistical data analysis, and mathematical reasoning.
  • Experience with CAPA and ability to analyze and problem‑solve.
  • Ability to work within a changing environment and engage a wide variety of personnel on all levels.
  • ASQ Certified Quality Engineer or other ASQ certifications are a plus.
  • Excellent written and verbal communication and presentation skills.
  • Ability to communicate across functional lines.
Physical Demands and Work Conditions
  • Sitting 60‑80%, standing & walking 20‑40%.
  • Repetitive work on computer 80%.
  • Must be able to work in a clean room environment and tolerate chemical odors.
  • Must be able to work in a lab environment and tolerate the smell and sight of blood.
Education

Bachelor’s Degree in Technical and Scientific disciplines (Engineering, Physics, Chemistry, or Biology).

Benefits and Compensation

Salary range: $85,000–$95,000 annually + annual bonus incentive.

Travel Requirements: Occasional travel may be required.

Equal Employment Opportunity

LivaNova values equality and diversity. The company is committed to ensuring that the recruitment process is fair, transparent, and free from unlawful discrimination. Selection is based on key demands/requirements for the role rather than bias or discrimination on the basis of legally protected classifications.

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