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Full Time Cdmo Jobs (NOW HIRING)

... CDMO environment is strongly preferred. Equivalent combination of education, technical training, certifications, and relevant experience may be accepted. Employment Type: FULL_TIME

VP, Supply Chain

Tustin, CA · On-site

$226K - $283K/yr

Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative ... This role is a full-time onsite position. Days and hours of work are Monday through Friday unless ...

Process Development Scientist

Denver, CO · On-site

$110K - $150K/yr

Denver, CO (on-site) Type: Full-time Cascade Biocatalysts is building the next generation of ... The ideal candidate comes from a CDMO or industrial process chemistry group, and is now ready to ...

Director, Manufacturing

Walkersville, MD · On-site +1

$198K - $232K/yr

The full-time base annual salary for this position is expected to range between $198,900 to $232 ... Demonstrated experience leading manufacturing operations within a CDMO environment, including ...

Process Development Scientist

Denver, CO · On-site

$110K - $150K/yr

Denver, CO (on-site) Type: Full-time Cascade Biocatalysts is building the next generation of ... The ideal candidate comes from a CDMO or industrial process chemistry group, and is now ready to ...

Project Manager

Bothell, WA · On-site

$94K - $129K/yr

Preferred: * 2+ years of CDMO experience. * Experience supporting late-stage programs, including ... Bothell, WA Schedule: Full-time Compensation: $94,000 - $129,250 Who We Are AGC Biologics is a ...

Director, Manufacturing

Walkersville, MD · On-site +1

$198K - $232K/yr

The full-time base annual salary for this position is expected to range between $198,900 to $232 ... Demonstrated experience leading manufacturing operations within a CDMO environment, including ...

Marketing Manager

Morgan Hill, CA · Remote

$100K - $125K/yr

Marketing Manager Morgan Hill, CA 95037 Full-Time | Exempt | Remote Make an Impact at Tecan Are you ... Tecan's CDMO offering, through integrated marketing campaigns, thought leadership, and close ...

The full-time base annual salary for this position is expected to range between $150,000 to $200 ... Minimum of 8 years of experience in biotechnology, pharmaceutical, CDMO, or life sciences ...

The full-time base annual salary for this position is expected to range between $150,000 to $200 ... Minimum of 8 years of experience in biotechnology, pharmaceutical, CDMO, or life sciences ...

Showing results 21-40

Full Time Cdmo information

See salary details

$15K

$241.3K

$387K

How much do full time cdmo jobs pay per year?

As of Aug 20, 2026, the average yearly pay for full time cdmo in the United States is $241,295.00, according to ZipRecruiter salary data. Most workers in this role earn between $200,000.00 and $300,000.00 per year, depending on experience, location, and employer.

What is a full time CDMO?

A Full Time CDMO refers to a professional working full time at a Contract Development and Manufacturing Organization (CDMO). CDMOs provide comprehensive services to pharmaceutical and biotechnology companies, including drug development, manufacturing, and sometimes packaging. A full-time role in a CDMO may involve responsibilities in research, production, quality control, or project management, depending on the position. Employees in these organizations play a crucial role in bringing new drugs to market efficiently and according to regulatory standards.

What are the key skills and qualifications needed to thrive as a full time CDMO?

To thrive as a Full-Time CDMO, you need deep expertise in digital marketing strategy, brand development, analytics, and a relevant degree in marketing or a related field. Familiarity with tools like Google Analytics, CRM systems (e.g., Salesforce), marketing automation platforms (e.g., HubSpot), and certifications such as Google Ads or Meta Blueprint are common requirements. Leadership, creativity, strong communication, and adaptability are crucial soft skills that set top CDMOs apart. These competencies ensure the organization can effectively leverage digital channels for growth, stay ahead of trends, and drive measurable results.

What are some common challenges faced when working in a full time CDMO role?

Working full-time at a Contract Development and Manufacturing Organization (CDMO) can be highly rewarding but comes with unique challenges. One common challenge is managing multiple projects for different clients simultaneously, which requires strong organizational and communication skills. Adapting quickly to the specific requirements and timelines of various clients is essential, as priorities can shift rapidly. Additionally, ensuring compliance with strict industry regulations and quality standards while maintaining efficiency can be demanding but is crucial for success in this environment.

What is the difference between Full Time Cdmo vs Contract Cdmo?

AspectFull Time CdmoContract Cdmo
Employment TypePermanent, full-timeTemporary, project-based
Work EnvironmentIn-house, company facilitiesOn-site or remote, client sites
Certifications & CredentialsTypically requiredOften required, but may vary
Industry UsageCommon in biotech and pharma companiesCommon for specific projects or trials

Full Time Cdmo roles involve permanent employment with a company, offering stability and ongoing responsibilities. Contract Cdmo positions are project-based, providing flexibility for specific trials or phases. Both roles require relevant industry certifications, but employment type influences job security and work structure.

More about Full Time Cdmo jobs

What cities are hiring for Full Time Cdmo jobs?

Cities with the most Full Time Cdmo job openings:

What are the most commonly searched types of Cdmo jobs?

The most popular types of Cdmo jobs are:

What states have the most Full Time Cdmo jobs?

States with the most job openings for Full Time Cdmo jobs include:

Infographic showing various Full Time Cdmo job openings in the United States as of August 2026, with employment types broken down into 98% Full Time, 1% Contract, and 1% Nights. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $241,295 per year, or $116 per hour.

IT Analyst I

Cambrex

High Point, NC • On-site

Full-time

Medical, Life, Retirement

Re-posted 4 days ago


Cambrex rating

8.1

Company rating: 8.1 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

38th of 86 rated pharmaceutical


Job description

Company Information

You Matter to Cambrex.

Cambrex is a leading global contract development and manufacturing organization (CDMO) that provides drug substance development and manufacturing across the entire drug lifecycle, as well as comprehensive analytical and IND enabling services. 

With over 40 years of experience and a team of 2,000 experts servicing global clients from North America and Europe, Cambrex offers a range of specialized drug substance technologies and capabilities, including continuous flow, controlled substances, liquid-phase peptide synthesis, solid-state science, material characterization, and highly potent APIs.

Your Work Matters.

At Cambrex, we strive to build a culture where all colleagues have the opportunity to:

  • engage in work that matters to our customers and the patients they serve
  • learn new skills and enjoy new experiences in an engaging and safe environment
  • strengthen connections with coworkers and the community

We're committed to attracting and nurturing a passionate team of valued professionals in our fast-paced and growing company.  We offer a competitive benefits package that includes healthcare, life insurance, planning for retirement, and more!

Your Future Matters.

Known for our customer-focused scientific and manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career and growth opportunities across our global network of locations. Together with our customers, we aim to improve the quality of life for patients around the world. Start a career where You Matter by applying today!

Overview:

The IT Analyst I provides on-site technical support and contributes to business systems analysis in a regulated GMP/CDMO environment. This role supports end-user systems, hardware, software, and local IT operations while assisting with documentation, process improvement, and system support activities. This role is ideal for a service-oriented IT professional who enjoys hands-on problem solving, working directly with users, and supporting operations in a fast-paced manufacturing setting.

Responsibilities:
  • Provide desktop and end-user support for computers, peripherals, and applications
  • Troubleshoot and resolve hardware, software, and network-related issues
  • Monitor system performance and resolve performance concerns
  • Install, configure, and maintain IT equipment and systems
  • Support user account management including Active Directory
  • Coordinate vendors and service providers
  • Gather and document business and system requirements
  • Assist with process mapping and system documentation
  • Support system testing, validation, and implementation
  • Assist with IT projects and continuous improvement initiatives
Qualifications / Skills:
  • Strong communication and customer service skills
  • Strong analytical and problem-solving skills
  • Ability to manage multiple priorities
  • Detail-oriented with strong documentation skills
  • Ability to work in a regulated environment
  • Self-starter who can work well independently or in groups.
  • Experience with business and technical requirements analysis, elicitation, modeling, verification, and methodology development.
  • Experience in process mapping and modelling.
  • Experience collaborating with corporate IT, site functions, and third-party vendors to support local business and operational needs
  • Ability to create, maintain, and follow support documentation, work instructions, and standard procedures
  • Preferred familiarity with GxP-regulated environments, including laboratory and/or manufacturing operations

Software Development Skills:           

  • Java/JavaScript/C#/.NET/Python
  • AWS/Azure
  • PowerBI
  • Knowledge of process mapping tools
  • Working knowledge of Project Management tools (JIRA, Asana, MS Project)
  • Experience designing and developing technical documentation for regulated software applications
  • Working knowledge of .NET, APIs and Webhooks
  • Knowledge of Web development methodologies like SCRUM, and Agile.
  • Excellent communication skills, both verbal and written
  • Understanding of ITIL and Safe frameworks. ITIL certified a plus.
Education, Experience, and Licensing Requirements: (Text Only)  Associate's degree in Information Technology, Computer Information Systems, Computer Science, or related field preferred; bachelor's degree also considered. Experience providing IT support in a regulated GMP/GxP, pharmaceutical, biotech, manufacturing, or CDMO environment is strongly preferred. Equivalent combination of education, technical training, certifications, and relevant experience may be accepted.    Employment Type: FULL_TIME

What Cambrex employees say

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Benefits

Hours and flexibility

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About Cambrex

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

East Rutherford, NJ, US

Year founded

1981

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