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Manager Cdmo Jobs in Colorado (NOW HIRING)

QA Product Specialist

Boulder, CO · On-site

$100K - $118K/yr

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO ... Project Management experience, although not required, is beneficial to this position. LANGUAGE ...

Senior Quality Assurance Specialist I

Longmont, CO · On-site

$81K - $112K/yr

Cambrex is a leading global contract development and manufacturing organization (CDMO) that ... Works with the site management in all areas to maintain a cGMP compliant facility in a constant ...

Lab Administrator

Boulder, CO · On-site

$26 - $32/hr

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO ... Brings waste to waste management and delivers new blue drums to the labs. Repair HPLC waste ...

New

QA Engineer

Boulder, CO · On-site

$90K - $108K/yr

CordenPharma is a leading full-service Contract Development and Manufacturing Organization (CDMO ... Ability to effectively present information to management and colleagues. MATHEMATICAL SKILLS ...

Showing results 21-40

Manager Cdmo information

What are the roles and responsibilities of a Manager CDMO?

A Manager CDMO (Contract Development and Manufacturing Organization) oversees the relationship and project management between a pharmaceutical or biotech company and external CDMO partners. Their responsibilities include coordinating project timelines, ensuring regulatory compliance, managing budgets, and facilitating communication between internal teams and the CDMO. They play a key role in ensuring that drug development and manufacturing projects meet quality standards and are delivered on time. The Manager CDMO also addresses any issues that arise during the project lifecycle and ensures alignment with company objectives.

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

To thrive as a Manager CDMO (Contract Development and Manufacturing Organization), you need a solid background in pharmaceutical or biotechnology processes, project management expertise, and a relevant science or engineering degree. Familiarity with quality management systems (QMS), regulatory compliance tools (like GMP, ISO), and project tracking software is typically required. Strong leadership, negotiation, and interpersonal communication skills help in managing cross-functional teams and client relationships. These skills and qualifications are vital for ensuring project success, regulatory adherence, and client satisfaction in a highly regulated and competitive industry.

How does a Manager CDMO typically interact with clients and internal teams to ensure project success?

A Manager CDMO (Contract Development and Manufacturing Organization) acts as a key liaison between clients and various internal departments such as R&D, quality assurance, and manufacturing. They coordinate project timelines, communicate client requirements, and address any issues that arise to keep projects on track. Effective collaboration and clear communication are essential, as managers often facilitate meetings, provide regular updates, and align cross-functional teams to meet client expectations and regulatory standards. This role requires strong organizational skills and the ability to adapt to shifting client needs.

What is the difference between Manager Cdmo vs Project Manager?

AspectManager CdmoProject Manager
CredentialsTypically requires life sciences or pharmaceutical management experience, relevant certifications (e.g., PMP, regulatory training)Requires project management certifications (e.g., PMP), often with industry-specific experience
Work EnvironmentWorks within pharmaceutical or biotech companies, overseeing clinical development or manufacturingWorks across industries, managing projects in various sectors including healthcare, IT, construction
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and contract manufacturing organizationsUsed across multiple industries, including healthcare, construction, IT, and engineering

The Manager Cdmo primarily focuses on managing contract development and manufacturing operations within the pharmaceutical industry, requiring specialized industry knowledge. In contrast, a Project Manager oversees various projects across industries, emphasizing project execution and delivery. While both roles involve leadership and coordination, the Manager Cdmo's expertise is more industry-specific, especially in regulated environments.

What are the most commonly searched types of Cdmo jobs in Colorado? The most popular types of Cdmo jobs in Colorado are:
What are popular job titles related to Manager Cdmo jobs in Colorado? For Manager Cdmo jobs in Colorado, the most frequently searched job titles are:
What cities in Colorado are hiring for Manager Cdmo jobs? Cities in Colorado with the most Manager Cdmo job openings:
Infographic showing various Manager Cdmo job openings in Colorado as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Director of Operations

Nissha Medical Technologies

Colorado Springs, CO • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


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

Director of Operations

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.

The primary responsibility of this position is to lead, direct, and support the daily operations of Nissha Medical Technologies Colorado Springs location, ensuring customer satisfaction and on-time production. The position is responsible for managing  effectiveness and profitability. This position is challenged with maintaining the vision and goals for the organization. The successful candidate will work with a high degree of autonomy, provide a high level of customer service, and teach and mentor less experienced team members with a focus on growing their ability and knowledge.

What You Will Do

  • Follow all employee guidelines and Quality Systems Regulations (QSR's) as defined by Nissha Medical Technologies practices, policies and Standard Operating Procedures (SOP's) to ensure that customer requirements and FDA (or equivalent) 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.
  • Provide motivational and organizational guidance and support to assigned areas by leading meetings, providing updates, scheduling work-related activities, and organizing daily operations to make the defined staff knowledgeable in their field and efficient in their job tasks.
  • Oversee manufacturing activities of multiple product lines operating on multiple shifts.
  • Develop and implement short- and long-term strategic plans to ensure manufacturing systems are in place to meet business objectives. 
  • Work cross-functionally with Engineering, Quality, Production and other departments as needed to ensure effective new product transitions into production. 
  • Work with Supply Chain management to develop effective production planning and inventory systems; ensure accurate tracking and accounting of materials. 
  • Work with Continuous Improvement and Engineering functions to develop effective manufacturing processes capable of meeting quality, cost and supply chain objectives.
  • Anticipate and resolves highest level issues and conflicts that could impact operations success. 
  • Provide direct day-to-day management to our team of Manufacturing Engineers and Technicians.
  • Provide indirect management to Production/Manufacturing, Maintenance and Facilities, and Logistics (Shipping, Receiving, Packaging and Warehouse) areas.
  • Hire and retain a diverse, highly qualified staff and provide ongoing performance feedback. 
  • Set goals which align to department plans and manage the execution of goals through coaching and mentoring. 
  • Maintain a safe and professional work environment. 
  • Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements 
  • Comply with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. 
  • Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
  • Abides by all safety and security rules set forth by the company and regulatory agencies
  • Regular attendance.
  • Performs other duties as assigned. 

What You Bring

Core Qualifications

  • Bachelor's degree in a relevant field.
  • A minimum of 8+ years of progressively responsible work experience in a high-volume, multi product manufacturing environment, preferably in the medical device industry.
  • Proven managerial experience.
  • Significant experience leading and implementing lean manufacturing/Six Sigma initiatives. 
  • Solid knowledge of GMP and ISO regulations.
  • Strong leadership skills, including the ability to set goals and provide positive and constructive feedback respectfully to build positive relationships and improve business results.
  • Ability to work effectively within a team in a fast-paced changing environment. 
  • Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization. 
  • Multi-tasks, prioritizes and meets deadlines in timely manner.
     

Preferred Qualifications

  • Advanced Degree in a relevant field.
     

Professional Traits We Value

  • Strong organizational, planning, and follow-up skills and ability to hold others accountable.
  • Strong analytical and problem-solving skills.
  • Ability to influence for results in a cross-functional organization.
  • Ability to provide change leadership and accelerate change.
  • Project management skills.
  • Ability to perform in fast paced environment.

Compensation & Benefits

The expected salary range for this position is $125,000 - $155,000 annually. 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.


What Nissha Medical Technologies employees say

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