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Full Time Cdmo Jobs (NOW HIRING)

Our leading CDMO client is eager to hire an Aseptic Downstream Process Development SME for their ... This is a full-time role directly with the client - an outstanding opportunity to join an ...

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to ... Proficiency in ERP systems and Microsoft Excel Please note that this role is a full-time onsite ...

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to ... Proficiency in ERP systems and Microsoft Excel Please note that this role is a full-time onsite ...

Warehouse Specialist

Pennington, NJ · On-site

$65K - $75K/yr

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to ... Proficiency in ERP systems and Microsoft Excel Please note that this role is a full-time onsite ...

Senior Process Engineer

Fishers, IN

$97.30K - $125.90K/yr

Additional Preferences: * CMO/CDMO experience Technical and/or lean six sigma certifications ... Employment Type: Full-Time

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Full Time Cdmo information

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$15K

$241.3K

$387K

How much do full time cdmo jobs pay per year?

As of May 29, 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 are the key skills and qualifications needed to thrive as a Full-Time CDMO (Chief Digital Marketing Officer), and why are they important?

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 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 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 May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $241,295 per year, or $116 per hour.
CDMO Product Development Technician I

CDMO Product Development Technician I

NorthStar Medical Radioisotopes, LLC

Madison, WI • On-site

Full-time

Posted 11 days ago


Job description

Overview

Join the best radiopharmaceutical company in the world!

If you're looking to make an impact while building a meaningful career in a specialized, fast-growing field, NorthStar Medical Radioisotopes is the place to do it. NorthStar Medical Radioisotopes is a growing, commercial-stage company focused on advancing patient care by providing therapeutic radioisotopes and novel radiopharmaceuticals to detect and treat cancer.

At the forefront of NorthStar's technological innovation is scientific excellence, using first-in-kind electron accelerator technology and integrated campus capabilities to drive progress in radiopharmaceutical manufacturing. Our work is driven by a meaningful mission-advancing life-saving radiopharmaceutical development and ensuring a reliable supply of critical medical isotopes for patients in need. As a rapidly growing organization operating on the cutting edge of science, we offer exceptional career growth and professional development opportunities, supported by world-class facilities and a competitive benefits package.

Position

The CDMO Product Development Technician I will provide support in NorthStar's radiologic science laboratories within the CDMO Product Development Department. Responsibilities include the ability to independently perform laboratory controls, maintenance and calibration of equipment, manifestation and disposal of radioactive material, preparation of laboratory solutions, assistance with product development/production, and general laboratory maintenance. This role will specialize in development, verification, and validation of current and/or new and existing radiopharmaceutical products/medical devices. 

Responsibilities
  • Perform routine and non-routine experiments and/or analyses following NorthStar procedures and guidelines. Ensure data is collected and documented according to good documentation practices.
  • With appropriate supervision, perform tasks as needed to support product development. This may include solution preparation, equipment checks, and documentation preparation.
  • Perform tasks as needed to support product development. This may include solution preparation, equipment checks, and documentation preparation.
  • Understand and execute the cradle-to-grave processes specific to all radioactive substances that are used in the laboratory including, but not limited, to DOT check in/check out process, waste management, and documentation/filing.
  • Maintain low-level radioactive waste inventory management including: storage, manifestation, and disposal in accordance with regulatory requirements.
  • Maintain supplies and manage inventory within the laboratory space.
Qualifications

Knowledge of ALARA principles required.  Previous experience in a nuclear pharmacy, nuclear medicine department, laboratory setting, or cGMP environment preferred.

CDMO Product Development Technician I

Associate's degree in a related science discipline or related medical field or completion of an accredited Nuclear Medicine Technology educational program required 

Please note the company cannot provide immigration-related sponsorship (including H-1B status, O-1 status, Optional Practical Training support, etc.) for this position.  Each successful applicant will be required to complete the Form I-9, Employment Eligibility Verification, demonstrating both identity and employment authorization, on or before the first day of employment.  Under federal law, only truthful information may be provided on the Form I-9.

Location

NorthStar Medical Radioisotopes is proud to call Beloit, Wisconsin home. Our headquarters and primary manufacturing facility are located in this vibrant, growing community that combines the charm of a small city with the advantages of a central Midwest location. Beloit features a lively, revitalized downtown filled with local restaurants, shops, and cultural events, and is just a short drive from major metropolitan areas including Madison, Milwaukee, Chicago, and Rockford.

Situated in the heart of the South Central Wisconsin and Northern Illinois region, Beloit offers a rare blend of urban amenities and scenic natural surroundings. Whether you're drawn to outdoor recreation, educational institutions, the arts, or historic landmarks, the area provides rich and diverse experiences for all interests. A variety of nearby communities, ranging from rural towns to suburban neighborhoods, offer flexible housing options and access to multiple school districts, making Beloit an excellent choice for individuals and families considering relocation.

NorthStar Medical Radioisotopes is an equal opportunity employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Employment Type: FULL_TIME