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Contract Manager Medical Device Jobs in Colorado

Citadel Security USA

Contract Manager

Thornton, CO · On-site

$25/hr

Respond appropriately to medical emergencies, fire alarms, evacuations, and other urgent situations ... Effective de-escalation and conflict-management skills. * Ability to make sound decisions during ...

Quantix

Project Manager

Lakewood, CO · On-site

They rank as one of the top medical device / services companies in the world, providing life saving ... Contract Length: 6 months+ Client located in Lakewood, Colorado is seeking a Project Manager for a ...

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Contract Manager Medical Device information

What does a contract manager in the medical device industry do?

A Contract Manager in the medical device industry is responsible for overseeing the drafting, negotiation, and administration of contracts related to the development, manufacturing, and distribution of medical devices. They ensure that all agreements comply with regulatory requirements, company policies, and industry standards. Their role helps safeguard the company’s interests while fostering strong relationships with suppliers, customers, and regulatory agencies. Additionally, they work closely with legal, sales, and compliance teams to mitigate risks and resolve contractual issues.

What are some common challenges a contract manager faces when working with medical device agreements?

Contract Managers in the medical device industry often navigate complex regulatory requirements while ensuring contracts align with both business objectives and compliance standards. Challenges may include negotiating terms that adhere to FDA regulations, managing intellectual property clauses, and coordinating among legal, sales, and regulatory teams. Success in this role often relies on strong attention to detail and the ability to balance multiple stakeholders’ interests. Staying updated on evolving industry standards can also be demanding but is crucial for effective contract management.

What are the key skills and qualifications needed to thrive as a contract manager in the medical device industry, and why are they important?

To excel as a Contract Manager in the Medical Device industry, you need expertise in contract law, negotiation, and regulatory compliance, often supported by a bachelor’s degree in business, law, or a related field. Familiarity with contract management software (such as Icertis or SAP Ariba), e-signature platforms, and knowledge of FDA or EU MDR regulations are typically required. Strong attention to detail, communication, and problem-solving skills help build trust and ensure effective collaboration with stakeholders. These abilities are crucial for minimizing risk, maintaining compliance, and supporting the commercial success of medical device products.

What is the difference between Contract Manager Medical Device vs Regulatory Affairs Specialist?

AspectContract Manager Medical DeviceRegulatory Affairs Specialist
CredentialsTypically requires a bachelor's degree in business, law, or related field; certifications like Certified Commercial Contracts Manager (CCCM) are commonRequires a degree in life sciences, pharmacy, or engineering; certifications like RAC (Regulatory Affairs Certification) are common
Work EnvironmentWorks primarily in legal, sales, or procurement departments within medical device companiesWorks in regulatory compliance departments, often collaborating with R&D and quality assurance teams
Employer & Industry UsageUsed across medical device manufacturers, suppliers, and healthcare organizationsUsed mainly in medical device, pharmaceutical, and biotech industries

The Contract Manager Medical Device focuses on negotiating and managing contracts related to medical devices, ensuring legal and commercial compliance. In contrast, the Regulatory Affairs Specialist ensures products meet regulatory standards for approval and market entry. Both roles are essential in the medical device industry but serve different functions related to compliance and legal agreements.

What are popular job titles related to Contract Manager Medical Device jobs in Colorado?

For Contract Manager Medical Device jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Contract Manager Medical Device jobs in Colorado look for?

The top searched job categories for Contract Manager Medical Device jobs in Colorado are:

What cities in Colorado are hiring for Contract Manager Medical Device jobs?

Cities in Colorado with the most Contract Manager Medical Device job openings:

Contract Manager Medical Device jobs near you
Infographic showing various Contract Manager Medical Device job openings in Colorado as of August 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 85% In-person, and 15% Remote job distribution.

Medical Device Assembler I

Colorado Springs, CO • On-site

Nissha Medical Technologies
Medical Equipment and Supplies Manufacturing • 1 - 5K employees
Learn more about Nissha Medical Technologiesexternal

$17 - $19.50/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 15 days ago

Nissha Medical Technologies rating

7.1

Company rating: 7.1 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

Job description

Medical Device Assembler I

About Nissha Medical Technologies

Nissha Medical Technologies (NMT) is a global Contract Development and Manufacturing Organization (CDMO) where people, purpose, and technology come together to advance healthcare. Headquartered in the United States, NMT is the medical devices business unit and a wholly owned subsidiary of Nissha Co., Ltd., a publicly traded Japanese company based in Kyoto, Japan (TSE: 7915).

Across our global organization, our teams collaborate to design and manufacture innovative medical devices and solutions that make a real difference in patients' lives. We partner closely with our customers to solve complex challenges, move ideas forward, and support products from concept through commercialization. Our work spans patient monitoring, surgical and interventional solutions, precision components, and emerging technologies, all grounded in a strong culture of quality, accountability, and continuous improvement.

At Nissha Medical Technologies, we believe our success is driven by our people. We foster an environment where curiosity is encouraged, teamwork is valued, and individuals are empowered to grow their skills and careers. If you're motivated by meaningful work, collaboration, and the opportunity to help shape the future of healthcare, you'll find a place to belong at NMT.

What You Will Do

The Medical Device Assembler will be a key member of our production team responsible for prepping assemblies and sub-assemblies for small, single-use medical devices. The ideal candidate will be quality-driven, have the ability to quickly come up to speed on existing production processes and be motivated to help develop and improve these processes. 

This is a 1st  Shift position working Monday through Thursday from 6:00am to 4:30pm. 

  • Follow Employee guidelines and Quality System Regulations as defined by Nissha Medical Technologies practices, policies and Standard Operating Procedures to ensure that customer requirements and industry standards and regulations are met.

  • Demonstrate knowledge and act in accordance with NMT's Employee Guidelines and applicable quality standards as outlined in NMT's Quality Manual.

  • Thoroughly reads and follows all job sheets, production drawings and Manufacturing Assembly Instructions.

  • Performs tin dipping, wire cutting, stripping, crimping, housing, ultra-sonic welding, bonding, wire routing, and various other tasks as assigned. 

  • Operates production machines at the discretion of the supervisor. 

  • Responsible for the quality of the product produced. 

  • Works well with various internal and external engineering and other support disciplines to perform troubleshooting, data collection and to resolve assembly problems.

  • Abides by all safety and security rules set forth by the company and regulatory agencies

  • Regular attendance is required.

What You Bring

Core Qualifications

  • High School Diploma or General Education Degree (GED) 

  • Ability to apply principles outlined in Quality System Regulations (QSRs/GMPs).
  • Ability to use basic hand tools such as micrometers, calipers, etc.
  • Ability to operate electrical and mechanical equipment and interpret results.
  • Attention to detail to ensure high quality work and to detect when there are issues with tooling, materials, processes and quality.
  • Ability to work on a computer with various programs to transact product within the production system and complete online training

  • The ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. 

  • The ability to read and comprehend simple instructions such as Manufacturing Assembly Instructions, Quality Standards and Standard Operating Procedures. 

  • The ability to perform simple writing tasks such as recording log entries, lot numbers and dates.

  • Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.

Preferred Qualifications

  • Previous related industry experience in medical device production is preferred but not required.

  • Previous experience in FDA/GMP/ISO environment is preferred but not required.


Professional Traits We Value

  • Problem-solving ability
  • Works well in a collaborative team environment

Compensation & Benefits

The expected salary range for this position is $17.00 - $19.50/hour. Actual compensation will be determined based on experience, skills, qualifications, and geographic location. 

In addition, Nissha Medical Technologies offers a competitive total rewards package including medical, dental, and vision coverage, 401(k) with company match, paid time off, life and disability insurance, and professional development opportunities.

Equal Opportunity Statement

Nissha Medical Technologies is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees and applicants and do not discriminate based on any protected status under applicable law.

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