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Manager Cdmo Jobs in Seattle, WA (NOW HIRING)

AGC Biologics

Project Manager

Bothell, WA · On-site

$94K - $129K/yr

Job Summary We are looking for a Project Manager to lead biologics programs across the full product ... Preferred: * 2+ years of CDMO experience. * Experience supporting late-stage programs, including ...

Septodont

Territory Manager - Seattle, WA

Seattle, WA · On-site

$85K/yr

... CDMO), we are proud to work every day to improve patients' health and well-being. Present in more ... The Territory Manager drives/reports all sales activities through the CRM system and works closely ...

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All JobsCdmo JobsManager Cdmo JobsManager Cdmo Jobs in Seattle, WA

Manager Cdmo information

See Seattle, WA salary details

$27.9K

$67.7K

$132K

How much do manager cdmo jobs pay per year?

As of Aug 20, 2026, the average yearly pay for manager cdmo in Seattle, WA is $67,741.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,800.00 and $78,000.00 per year, depending on experience, location, and employer.

What are the roles and responsibilities of a Manager CDMO?

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.

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 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.

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.

What are the most commonly searched types of Cdmo jobs in Seattle, WA?

The most popular types of Cdmo jobs in Seattle, WA are:

What are popular job titles related to Manager Cdmo jobs in Seattle, WA?

For Manager Cdmo jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Manager Cdmo jobs in Seattle, WA look for?

The top searched job categories for Manager Cdmo jobs in Seattle, WA are:

Manager Cdmo jobs near you

Manager, Clinical Supply Operations

Immunome, Inc.

Bothell, WA • On-site

Full-time

Posted 16 days ago

Job description

Position Overview

The Manager, Clinical Supply Operations, is responsible for meeting Immunome's supply requirements by enabling and overseeing cGMP operations performed at Contract Development and Manufacturing Organizations (CDMOs). This role centers on managing the supply of finished drug products (FDP) and may support a wide range of projects, including biologics and small molecule programs.   

Responsibilities

  • Serve as the Supplier Relationship Manager (SRM) for specified CDMOs offering clinical packaging and distribution services. Serve as the primary liaison between the CDMO and Immunome.  
  • Lead one or more Virtual Management Teams (VMTs) ensuring Immunome's deliverables stay on track, and internal alignment on priorities and key communications with the CDMO.  
  • Conduct well-organized meetings with CDMOs. Ensure CDMO progress is tracking to plan (e.g., label development, production readiness, batch operations, release activities and logistics, etc.). Proactively address delays to avoid impact on supply.  
  • Participate in Clinical Operations study team(s) to stay current on trial design, demand parameters and protocol amendments. May support the development of randomization schemes for open and blind clinical studies.  
  • Partner with Supply Chain Planning to analyze inventory levels and plan batch production. Recommend changes to labeling and packaging schedules based on study progress.  
  • Support technical reviews of master and executed batch records, specifications, investigations, and change requests as required.  
  • Work with Global Logistics and Materials Management to ensure on-time shipments and drug availability at all clinical sites.  
  • Collaborate with department management and Legal to support the development and negotiation of proposals and service agreements.  
  • Monitor and track spending against budget. Ensure CDMO invoicing is accurate and aligned with contractual terms. Ensure that unexpected cost variances are communicated quickly. 
  • Maintain comprehensive knowledge of the CDMO's systems, capabilities, capacities, requirements, and business practices.  
  • Monitor CDMO performance through Key Performance Indicators (KPIs) and drive improvements aligned with Immunome's expectations. Lead or participate in periodic Business Review Meetings.  
  • Support sourcing efforts, and the audit and qualification of new CDMOs.  
  • Support technology transfers, process improvements, process validations, and regulatory submission reviews.  
  • Support network risk assessments and the development and implementation of measures to mitigate supply risks.  

Qualifications

  • Minimum of 5 years of experience with direct responsibility overseeing outsourced cGMP clinical packaging and labeling operations withing the biotech or pharmaceutical industry, or equivalent.
  • APICS certification a plus. 
  • Position will require domestic and international travel (up to 25%) and occasional evening and/or weekend commitment.     

Knowledge and Skills

  • Strong organizational, communication, and collaboration skills.  
  • Closely familiar with cGMP clinical labeling and packaging operations. Experience with highly potent products is a plus.   
  • Experience with IRT/RTSM systems supporting inventory and supply management functionality.   
  • Close familiarity or expertise working with an enterprise level planning system (ERP) is desired.  
  • Well-versed in Quality systems, and some direct experience with cGMP deviation investigations, change controls, and corrective actions.  
  • Possess negotiation skills and be familiar with general contractual terms.   
  • Comfortable with ambiguity and uncertainty; must adapt swiftly with focus on delivering to the business needs as priorities develop/change. 

Apply