1

Project Manager Cdmo Jobs in Everett, WA (NOW HIRING)

Project Manager

Bothell, WA · On-site

$94 - $129.25/hr

This role is a Project Manager for biologics programs across the full product lifecycle ... Preferred * 2+ years of CDMO experience. * Experience supporting late-stage programs, including PPQ ...

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 ...

... may support a wide range of projects, including biologics and small molecule programs ... Ensure CDMO progress is tracking to plan (e.g., label development, production readiness, batch ...

next page

Showing results 1-20

Project Manager Cdmo information

See Everett, WA salary details

$49.2K

$106.7K

$170.7K

How much do project manager cdmo jobs pay per year?

As of Sep 5, 2026, the average yearly pay for project manager cdmo in Everett, WA is $106,667.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,800.00 and $124,800.00 per year, depending on experience, location, and employer.

What is a project manager CDMO?

A Project Manager CDMO (Contract Development and Manufacturing Organization) is responsible for overseeing pharmaceutical or biotech projects outsourced to CDMOs. They coordinate between clients and internal teams to ensure timely delivery, quality, and compliance with regulatory standards. Their role includes managing project timelines, budgets, and resources, as well as communicating progress and addressing issues that may arise during drug development and manufacturing processes.

How does a project manager at a CDMO typically coordinate between clients and internal teams throughout a project lifecycle?

A Project Manager at a Contract Development and Manufacturing Organization (CDMO) acts as the central point of contact for clients and internal teams, ensuring clear communication and alignment of project goals. They regularly facilitate meetings, track project milestones, and proactively address potential issues or changes in scope. This involves close collaboration with departments such as R&D, manufacturing, quality assurance, and regulatory affairs to meet client expectations and project timelines. Effective project managers also document progress and maintain transparent reporting to both clients and internal stakeholders.

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

To excel as a Project Manager in a CDMO, you need a strong background in project management, life sciences, and regulatory compliance, often supported by a relevant degree and PMP certification. Familiarity with project management software (like MS Project or Smartsheet), quality management systems, and industry-specific regulations such as GMP are typically required. Outstanding organizational, communication, and stakeholder management skills help you effectively coordinate cross-functional teams and client expectations. These competencies are vital for delivering complex projects on time and within budget while maintaining regulatory standards and client satisfaction.

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

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

What cities near Everett, WA are hiring for Project Manager Cdmo jobs?

Cities near Everett, WA with the most Project Manager Cdmo job openings:

Infographic showing various Project Manager Cdmo job openings in Everett, WA as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 79% Physical, 9% Hybrid, and 12% Remote job distribution, with an average salary of $106,667 per year, or $51.3 per hour.

$94 - $129.25/hr

Other

Re-posted 19 days ago


AGC Biologics rating

7.5

Company rating: 7.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

65th of 86 rated pharmaceutical


Job description

Overview

Join Us in Bringing Hope to Life. Our purpose is to bring hope to life by enabling life‑changing therapies for patients around the globe, creating a healthier and happier tomorrow. We value excellence, collaboration, and meaningful work. This role is a Project Manager for biologics programs across the full product lifecycle.

Responsibilities
  • Lead CMC development, technology transfer, and GMP manufacturing programs from project initiation through close-out.
  • Develop and maintain project plans to ensure delivery within scope, timeline, and budget.
  • Serve as the primary point of contact for clients, providing clear communication and program leadership.
  • Partner with Business Development to strengthen client relationships and support program growth.
  • Identify project risks, develop mitigation strategies, and facilitate issue resolution with functional leaders.
  • Establish contingency plans and escalate critical issues as needed.
  • Drive alignment across Process Development, Analytical, QC, QA, MSAT, Supply Chain, and Manufacturing teams.
  • Support late-stage activities including PPQ readiness, regulatory submissions, and commercialization efforts.
  • Apply technical understanding of biologics development and manufacturing to support decision-making and technology transfer activities.
  • Manage project financials and contractual commitments, including Project Change Orders.
  • Provide milestone updates and forecasting information to support financial planning and client invoicing.
Qualifications & Experience
  • Required: Bachelor’s degree in Life Sciences, Chemistry, Biotechnology, Engineering, or a related field.
  • 3–8 years of experience within biopharmaceutical, biotechnology, or CDMO environments.
  • 2–5 years of direct project management experience.
  • Strong knowledge of GMP regulations and regulated manufacturing environments.
  • Experience with project management tools such as PPM systems or Smartsheet.
Preferred
  • 2+ years of CDMO experience.
  • Experience supporting late-stage programs, including PPQ, BLA preparation, and commercialization activities.
  • Experience leading technology transfers and new product introductions.
  • Familiarity with TrackWise.
Location & Schedule

Location: Bothell, WA • Schedule: Full-time

Compensation

Compensation: $94,000 – $129,250

About AGC Biologics

AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in the United States. From our headquarters in Bothell, Washington, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. We work with our team members across Europe, the U.S., and Japan to deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cell therapies. We are a collaborative, inclusive, and equal‑opportunity organization where team members are valued for their expertise, teamwork, and ingenuity. We invite you to explore our current opportunities and join our journey.

#J-18808-Ljbffr

What AGC Biologics employees say

Pay

Hours and flexibility

Workplace

Get the full story on Breakroom