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Full Time Cdmo Jobs (NOW HIRING)

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

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 ...

MedPharm

Project Manager

Durham, NC · On-site

Project Manager Onsite | Durham, NC | Full-Time Position Summary - The Project Manager plays a critical role in leading and executing client programs across MedPharm's end-to-end CDMO services. This ...

GenScript/ProBio

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 ...

GenScript/ProBio

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 ...

Adecco

USA Scientist I Scientific

Waltham, MA · On-site

$57/hr

Waltham, MA Schedule: Full-Time | Onsite Pay Rate: Up to $57.00/hour Assignment Type: Contract ... Experience with technology transfer and CDMO management * Knowledge of product comparability and ...

Biosimilar Sciences PR LLC

PR · On-site

... reputed CDMO, and extensive experience interacting with global regulatory agencies. Key ... Ability and willingness to relocate to Aguadilla, Puerto Rico , and work full-time on site.

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All JobsFull Time Cdmo Jobs

Full Time Cdmo information

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$15K

$241.3K

$387K

How much do full time cdmo jobs pay per year?

As of Jun 19, 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 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.

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 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 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.
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:
What job categories do people searching Full Time Cdmo jobs look for? The top searched job categories for Full Time Cdmo jobs are:
Full Time Cdmo jobs near you
Infographic showing various Full Time Cdmo job openings in the United States as of June 2026, with employment types broken down into 64% Full Time, 35% Part Time, and 1% Temporary. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $241,295 per year, or $116 per hour.

Aseptic Process Development - CDMO

MEDVACON

IN • On-site

Full-time

Posted 19 days ago

Job description

Company Description
MEDVACON Life Sciences works with many leading pharmaceutical companies to hire consulting, contract and full-time employees to join client organizations.
Our focus is cGMP Quality and Compliance, Validation and Regulatory for pharmaceutical and biotechnology companies.
Our leading CDMO client is eager to hire an Aseptic Downstream Process Development SME for their Indianapolis site. This is a full-time role directly with the client - an outstanding opportunity to join an innovative company developing brilliant biotechnology.
A successful background will be strong in Lab, Process and Analytical development including working knowledge of cGMPs related to the production of viral therapeutics and the ability to interface successfully with multi-disciplined teams.
Job Description
Direct the development and establishment of processes in GMP.
Accountable for developing a scalable platform for viral vector production processes that minimizes the risk during Process Development to GMP scale-up.
Provide technical expertise and leadership in science & technology and requires close collaboration with internal stakeholders.
If you're interested so far - apply! A member of our talent team will contact you and share comprehensive job details.
Qualifications
Bachelors Degree
5+ years exp in a cGMP pharma/biotech setting
Solid foundation in the fundamentals of biochemical engineering, virology and cell biology
Pharmaceutical industry experience in technical support of cGMP manufacturing and/or process development, including experience with Contract Development and Manufacturing Organizations
Experience with cell culture technologies, molecular biology, and aseptic processing
Additional Information
Please attach a WORD resume to your submission
All of your information will be kept confidential according to EEO guidelines.
ON-SITE only
This is a FT role and will include a full benefits package
40-hour week
NO AGENCIES please

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