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Project Manager Cdmo Jobs in Washington, DC (NOW HIRING)

GMP Senior Project Manager

Silver Spring, MD ยท On-site

$110K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

CDMO project management experience.Capital project management experience.SmartSheet experience.Leadership experience.Physical Requirements, Workplace Hazards and Conditions, and PPE and Chemical ...

GMP Senior Project Manager

Silver Spring, MD ยท On-site

$110K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

CDMO project management experience. * Capital project management experience. * SmartSheet experience. * Leadership experience. Physical Requirements, Workplace Hazards and Conditions, and PPE and ...

GMP Project Manager

Silver Spring, MD ยท On-site

$101K - $124K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

CDMO project management experience. * Capital project management experience. * SmartSheet experience. * Leadership experience. Physical Requirements: The physical requirements, workplace hazards and ...

GMP Project Manager

Silver Spring, MD ยท On-site

$101K - $124K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

CDMO project management experience.Capital project management experience.SmartSheet experience.Leadership experience.Physical Requirements:The physical requirements, workplace hazards and conditions ...

Quality Control Data Reviewer I

Germantown, MD ยท On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... Experience with project management tools such as Smartsheet preferred. * Ability to work ...

New

Quality Control Data Reviewer I

Germantown, MD ยท On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience with project management tools such as Smartsheet preferred. * Ability to work ... Professional development and career growth opportunities within a leading global CRO/CDMO Ready to ...

New

Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services ... or CDMO environment. * Direct hands-on experience authoring and revising GxP validation documents ...

New

Quality Control Data Reviewer I

Germantown, MD ยท On-site

$68K - $75K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... Experience with project management tools such as Smartsheet preferred. * Ability to work ...

New

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Showing results 1-20

Project Manager Cdmo information

See Washington, DC salary details

$50.4K

$109.4K

$175K

How much do project manager cdmo jobs pay per year?

As of Aug 12, 2026, the average yearly pay for project manager cdmo in Washington, DC is $109,363.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,900.00 and $128,000.00 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.

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.

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 popular job titles related to Project Manager Cdmo jobs in Washington, DC? For Project Manager Cdmo jobs in Washington, DC, the most frequently searched job titles are:
What job categories do people searching Project Manager Cdmo jobs in Washington, DC look for? The top searched job categories for Project Manager Cdmo jobs in Washington, DC are:

Bilingual (English & Chinese) Project Coordinator/Manager - CDMO Service

uBriGene Biosciences International Co

Germantown, MD โ€ข On-site

$60K - $100K/yr

Full-time

Posted 20 days ago


Job description

Position Summary:
We are seeking an individual with a strong background in viral vector production and/or project management. This position reports to VP of Commercial Strategy
  • Provide project management support to CMC team members including PD, TT and GMP teams in their execution of activities including manufacturing and release of drug substance and drug product, manufacturing process improvements and validation, analytical method development, transfer and validation, and shipping studies.
  • Serve as the primary liaison between uBriGene and clients on CMC activities for the client projects.
  • Collect updates on all CMC activities in the MS Project file on a monthly basis to update % completion or new dates.
  • Schedule, conduct, and draft minutes for PD, TT and GMP team on respective client projects to ensure regular, efficient team, and stakeholder communication.
  • Facilitate robust communication within PD, TT and GMP teams to ensure all functions are aware of the schedule, changes in strategy and impacts to risks and resources.
  • Hold team members accountable for on-time completion of tasks or milestones.
  • Performs critical path analysis and supports scenario planning for CMC deliverables.
  • Provide project coordination and communication, including participation in technical calls and face-to-face meetings, development of agendas, creation of meeting minutes, tracking of action items, and scheduling of follow-up meetings.
  • Support writing, review, and schedule of CMC related regulatory documents and health authority interactions.
  • Assist in preparing presentations, updating corporate project plans, etc.
  • Other responsibilities as needed

II. Requirements
Education, Experience, and Skills
  • B.S. or MS. in engineering or biological sciences degree is required
  • > 3 years of experience in biologics manufacturing, preferably in viral vector production
  • Previous project management experience in the biologics production is preferred but not required.
  • Proven experience organizing, planning, and executing large-scale projects from vision through implementation
  • Experience using project management tools (project scheduling and resource management), such as MS Project.
  • Proven analytical, conceptual and problem solving skills are required to evaluate business problems and apply knowledge to identify appropriate solutions.
  • Exceptional team building and stakeholder relationship management skills are required, with the ability to establish rapport, persuade and effectively negotiate with senior management, key stakeholders and functions.
  • Bilingual skills in English and Chinese are preferred.

uBriGene Biosciences, Inc. is an equal employment opportunity employer and does not discriminate against any applicant on the basis of race, color, religion, sex, sexual orientation, gender expression and identity, national origin, ancestry, age, mental and physical disability, genetic information, any veteran status, military status or application for military service, or membership in any other category protected under applicable law.