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Cdmo Consultant Jobs (NOW HIRING)

MEDVACON

Aseptic Process Development - CDMO

IN · On-site

... consulting, contract and full-time employees to join client organizations. Our focus is cGMP ... Our leading CDMO client is eager to hire an Aseptic Downstream Process Development SME for their ...

ProPharma Group

... consulting solutions that de-risk and accelerate our partners' most high-profile drug and device ... Previous experience managing CDMO partners would be highly preferred * Fluent in English

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How much do cdmo consultant jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for cdmo consultant in the United States is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $49.52 per hour, depending on experience, location, and employer.

What is a CDMO consultant?

A CDMO consultant is a professional who provides expert guidance to companies working with Contract Development and Manufacturing Organizations (CDMOs) in the pharmaceutical, biotechnology, or life sciences industries. They help businesses navigate the complexities of outsourcing drug development and manufacturing, ensuring regulatory compliance, efficient project management, and optimal partner selection. CDMO consultants often offer strategic advice on process optimization, technology transfer, and quality assurance. Their expertise can help companies accelerate product development timelines and reduce risks associated with outsourced manufacturing.

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

To thrive as a CDMO (Contract Development and Manufacturing Organization) Consultant, you need a solid background in pharmaceutical sciences, biotechnology, or chemistry, often supported by an advanced degree and industry experience. Familiarity with regulatory frameworks (such as FDA, EMA), quality management systems, and project management tools is typically required. Strong communication, problem-solving, and client relationship management skills set top consultants apart. These abilities are crucial for ensuring regulatory compliance, effective project delivery, and successful partnerships between clients and CDMOs.

What are some typical challenges faced by a CDMO consultant when managing client projects?

As a CDMO Consultant, you will often encounter challenges such as aligning client expectations with regulatory requirements, managing cross-functional project timelines, and ensuring effective communication between clients and internal teams. Navigating the complexities of technology transfer, process optimization, and quality compliance are also frequent hurdles. Success in this role requires strong project management skills, the ability to adapt to changing priorities, and a collaborative approach to problem-solving.

What are popular job titles related to Cdmo Consultant jobs?

For Cdmo Consultant jobs, the most frequently searched job titles are:

Infographic showing various Cdmo Consultant job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, and 5% Contract. Highlights an 79% Physical, 4% Hybrid, and 17% Remote job distribution, with an average salary of $86,430 per year, or $41.6 per hour.

Aseptic Process Development - CDMO

IN • On-site

MEDVACON
See more jobs at MEDVACONexternal

Full-time

Re-posted 15 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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