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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 ...

Avid Bioservices

Associate, Business Operations

Tustin, CA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

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

BioMADE

Shift Supervisor

Maple Grove, MN · On-site

$95K - $115K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Network Planning and Operational Structure Employment Type: Full Time Location: Maple Grove, MN ... Operating as a contract development and manufacturing organization (CDMO), this pilot plant will ...

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 ...

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 ...

MEDPHARM Corp

Project Manager

Durham, NC

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 ...

Pacelabs

Quality Manager- GMP Analytical Testing Site

Lebanon, NJ · On-site

$115K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a full-time Quality Manager Position located in Lebanon, NJ, Monday - Friday, from 8:30 a.m ... Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing ...

Pace

Quality Manager- GMP Analytical Testing Site

Lebanon, NJ · On-site

$115K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This is a full-time Quality Manager Position located in Lebanon, NJ, Monday - Friday, from 8:30 a.m ... Operating across a network of CDMO sites, GMP analytical testing laboratories, and manufacturing ...

Kalon Search

President

Manhattan, NY · On-site

$300K/yr

Lead in a true CDMO / contract manufacturing model--managing to customer specifications, timelines ... Ideally full-time onsite presence; a realistic minimum of 3 days per week onsite is expected.

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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 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:

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 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.

Aseptic Process Development - CDMO

MEDVACON

IN • On-site

Full-time

Re-posted 21 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

Apply