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Director Of Operations Cdmo Jobs (NOW HIRING)

Director of Operations

Memphis, TN · On-site

$70K - $75K/yr

Director of Operations Reports To: Franchise Owners, Regional Executive Director of Operations Pay rate: $70,000-75,000/yearly Location: Signal of Memphis [This role may involve supporting operations ...

Director of Operations

Bronx, NY · On-site

$57K - $77K/yr

The Director of Operations works in collaboration with the Director of Social Services and clinical staff to ensure the safety of all clients. The Director of Operation also supervises all operations ...

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Director Of Operations Cdmo information

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$34K

$107.7K

$179.5K

How much do director of operations cdmo jobs pay per year?

As of Sep 11, 2026, the average yearly pay for director of operations cdmo in the United States is $107,680.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $135,500.00 per year, depending on experience, location, and employer.

What are the roles and responsibilities of a director of operations in a CDMO?

A Director of Operations at a Contract Development and Manufacturing Organization (CDMO) oversees the daily operations and strategic direction of manufacturing and development services for pharmaceutical and biotechnology clients. Their responsibilities typically include managing production processes, ensuring compliance with regulatory standards, optimizing operational efficiency, and leading cross-functional teams. They also play a key role in client relationship management, resource allocation, and continuous improvement initiatives. This role requires a strong background in operations management, quality assurance, and knowledge of Good Manufacturing Practices (GMP).

What skills and qualifications are needed to thrive as a director of operations in a CDMO?

To thrive as a Director of Operations in a CDMO (Contract Development and Manufacturing Organization), you need expertise in pharmaceutical manufacturing processes, regulatory compliance, and a degree in life sciences, engineering, or a related field. Familiarity with GMP (Good Manufacturing Practices), ERP systems, and quality management tools is typically required, along with certifications like Six Sigma or Lean Manufacturing. Strong leadership, strategic thinking, and exceptional communication skills are vital for managing cross-functional teams and client relationships. These competencies ensure operational excellence, regulatory adherence, and client satisfaction in a highly regulated and competitive industry.

What are the key challenges a director of operations faces in a CDMO environment, and how can they be addressed?

A Director of Operations in a CDMO (Contract Development and Manufacturing Organization) often navigates complex challenges such as balancing client expectations, ensuring regulatory compliance, and managing production timelines across multiple projects. The fast-paced nature of the role requires strong cross-functional collaboration with quality assurance, supply chain, and project management teams. Proactively communicating with clients and internal stakeholders, staying updated on regulatory changes, and implementing robust process optimization strategies are critical to overcoming these challenges and ensuring operational excellence.

What is the difference between Director Of Operations Cdmo vs Quality Assurance Manager?

AspectDirector Of Operations CdmoQuality Assurance Manager
CredentialsRelevant degrees in life sciences, management certificationsQuality assurance certifications, such as CQE or ISO auditor
Work EnvironmentCDMO facilities, overseeing manufacturing and operationsLaboratories, quality control departments within pharmaceutical or biotech companies
Employer & IndustryContract Development & Manufacturing Organizations in biotech/pharmaPharmaceutical and biotech companies focusing on product quality

The Director Of Operations Cdmo primarily manages overall manufacturing and operational strategies within a CDMO setting, ensuring project delivery and compliance. In contrast, a Quality Assurance Manager focuses on maintaining product quality standards, conducting audits, and ensuring regulatory compliance. While both roles require industry-specific credentials and work within biotech/pharma environments, their core responsibilities differ: one oversees operations, the other ensures quality assurance.

What are popular job titles related to Director Of Operations Cdmo jobs?

For Director Of Operations Cdmo jobs, the most frequently searched job titles are:

Infographic showing various Director Of Operations Cdmo job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, 1% Temporary, 1% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $107,680 per year, or $51.8 per hour.

Director of Operations

Colorado Springs, CO • On-site

Nissha Medical Technologies, Ltd.
Medical Equipment and Supplies Manufacturing • 1 - 5K employees

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 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

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.

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