ZipRecruiter

Log In

1

Manager Cdmo Jobs (NOW HIRING)

Lantheus

Supply Chain Manager

Springfield, NJ · On-site

Lead and manage CDMO vendor relationships, including establishment of Master Service Agreements and service contracts. * Collaborate with Legal on new work orders, vendor agreements, and advice as ...

Lantheus

Supply Chain Manager

Springfield, NJ

Lead and manage CDMO vendor relationships, including establishment of Master Service Agreements and service contracts. * Collaborate with Legal on new work orders, vendor agreements, and advice as ...

Pharmaron

Finance Director, CDMO Operations

Coventry, RI · On-site

$180K - $240K/yr

Finance Director, CDMO Operations Salary Range: $180K - $240K (DOE) Location: Coventry, RI (On-site ... Manage vendor setup and change processes ensuring adherence to company controls and procedures

Pharmaron

Finance Director, CDMO Operations

Coventry, RI · On-site

$180K - $240K/yr

Finance Director, CDMO Operations Salary Range: $180K - $240K (DOE) Location: Coventry, RI (On-site ... Manage vendor setup and change processes ensuring adherence to company controls and procedures

next page

Showing results 1-20

All JobsCdmo JobsManager Cdmo Jobs

Manager Cdmo information

See salary details

$24.5K

$59.5K

$116K

How much do manager cdmo jobs pay per year?

As of Jul 10, 2026, the average yearly pay for manager cdmo in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 per year, depending on experience, location, and employer.

What are Manager CDMO roles and responsibilities?

A Manager CDMO (Contract Development and Manufacturing Organization) oversees the relationship and project management between a pharmaceutical or biotech company and external CDMO partners. Their responsibilities include coordinating project timelines, ensuring regulatory compliance, managing budgets, and facilitating communication between internal teams and the CDMO. They play a key role in ensuring that drug development and manufacturing projects meet quality standards and are delivered on time. The Manager CDMO also addresses any issues that arise during the project lifecycle and ensures alignment with company objectives.

What are the key skills and qualifications needed to thrive as a Manager CDMO, and why are they important?

To thrive as a Manager CDMO (Contract Development and Manufacturing Organization), you need a solid background in pharmaceutical or biotechnology processes, project management expertise, and a relevant science or engineering degree. Familiarity with quality management systems (QMS), regulatory compliance tools (like GMP, ISO), and project tracking software is typically required. Strong leadership, negotiation, and interpersonal communication skills help in managing cross-functional teams and client relationships. These skills and qualifications are vital for ensuring project success, regulatory adherence, and client satisfaction in a highly regulated and competitive industry.

How does a Manager CDMO typically interact with clients and internal teams to ensure project success?

A Manager CDMO (Contract Development and Manufacturing Organization) acts as a key liaison between clients and various internal departments such as R&D, quality assurance, and manufacturing. They coordinate project timelines, communicate client requirements, and address any issues that arise to keep projects on track. Effective collaboration and clear communication are essential, as managers often facilitate meetings, provide regular updates, and align cross-functional teams to meet client expectations and regulatory standards. This role requires strong organizational skills and the ability to adapt to shifting client needs.

What is the difference between Manager Cdmo vs Project Manager?

AspectManager CdmoProject Manager
CredentialsTypically requires life sciences or pharmaceutical management experience, relevant certifications (e.g., PMP, regulatory training)Requires project management certifications (e.g., PMP), often with industry-specific experience
Work EnvironmentWorks within pharmaceutical or biotech companies, overseeing clinical development or manufacturingWorks across industries, managing projects in various sectors including healthcare, IT, construction
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and contract manufacturing organizationsUsed across multiple industries, including healthcare, construction, IT, and engineering

The Manager Cdmo primarily focuses on managing contract development and manufacturing operations within the pharmaceutical industry, requiring specialized industry knowledge. In contrast, a Project Manager oversees various projects across industries, emphasizing project execution and delivery. While both roles involve leadership and coordination, the Manager Cdmo's expertise is more industry-specific, especially in regulated environments.

More about Manager Cdmo jobs
What cities are hiring for Manager Cdmo jobs? Cities with the most Manager 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 Manager Cdmo jobs? States with the most job openings for Manager Cdmo jobs include:
What job categories do people searching Manager Cdmo jobs look for? The top searched job categories for Manager Cdmo jobs are:
Manager Cdmo jobs near you
Infographic showing various Manager Cdmo job openings in the United States as of July 2026, with employment types broken down into 2% Locum Tenens, 42% Internship, 48% Full Time, 1% Contract, 1% Nights, and 6% Summer. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $59,525 per year, or $28.6 per hour.

CDMO Project Manager

The businesses of Merck KGaA, Darmstadt, Germany

Saint Louis, MO • On-site

$89K - $133K/yr

Full-time

Medical, Retirement, PTO

Posted 13 days ago

Job description

Work Your Magic with us!Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.


Your Role

We are looking for a successful, true Project Manager for our Cherokee CDMO (Custom Development Manufacturing Organization) site in St. Louis. In this position you will play a critical role in leading, planning, and executing complex projects from inception to completion. You will ensure projects - ranging from facility expansions to new product launches - are delivered on time, within scope, and on budget while managing cross-functional team dynamics. Key responsibilities include the following:

  • Own and execute complex, fast-paced projects (expansions, new products, operational excellence) from scope through to delivery
  • Partner with internal and external stakeholders, leveraging strong interpersonal skills to influence teams without direct authority
  • Proactively identify project risks, collaborate with key stakeholders to resolve critical issues, and minimize organizational impact
  • Facilitate productive meetings for diverse audiences and provide regular, proactive progress updates to clients and leadership
  • Create and maintain essential project artifacts, including charters, schedules, budgets, change controls, and risk logs
  • Mentor and coach project management personnel across the organization, capturing lessons learned for continuous improvement

Who You Are

Minimum Qualifications:

  • Bachelor's degree in engineering or life science discipline and 5+ years of Project Management experience

OR

  • High School Diploma or GED with 10+ years of Project Management experience

Preferred Qualifications:

  • PMP Certification and proficiency with Smartsheet or equivalent project management tools
  • Proven project management experience within a highly regulated GMP, Biotech, or Pharma manufacturing environment
  • Strong familiarity with FDA, EMA, and other global regulatory standards
  • Independent self-starter with a track record of driving cross-functional results in biopharmaceutical operations
  • Exceptional attention to detail with experience in meticulous document review and strict adherence to procedures
  • Strong analytical and problem-solving skills with the ability to identify risks and communicate them clearly
  • Excellent oral and written communication skills across all levels of internal and external stakeholder

Salary range for this position: $89,000 - $133,600 annually

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information clickhere.


What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Employment Type: FULL_TIME

Apply