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Project Manager Cdmo Jobs in Washington (NOW HIRING)

GMP Senior Project Manager

Silver Spring, MD ยท On-site

$110K - $130K/yr

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

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

Ability to lead projects or workstreams * Ability to manage and prioritize multiple tasks in a fast ... CDMO, distribution, healthcare providers, payors, and healthtech. Recruiting for this role ends on ...

Coordinate with PMO as Technology Transfer Lead on multiple CDMO projects, conducting regular project meetings and driving project execution, scheduling, monitoring of budgets, technical decision ...

MSAT mRNA/DNA Scientist

Silver Spring, MD ยท On-site

$92K - $124K/yr

Coordinate with PMO as Technology Transfer Lead on multiple CDMO projects, conducting regular project meetings and driving project execution, scheduling, monitoring of budgets, technical decision ...

... CDMO (Contract Development and Manufacturing Organization), clinical technology, or life sciences ... Strong project management skills and ability to manage multiple events and sales initiatives ...

... CDMO site. In this temporary assignment, you will partner with Corporate Learning, Site Leadership ... Demonstrated project management skills. * Understanding or familiarity with relevant FDA, EMA, ICH ...

Cost Accountant

Rockville, MD ยท Hybrid

$66K - $89K/yr

... CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging ... projects. * Detail-oriented with strong organizational skills and ability to manage multiple ...

Laboratory Assistant

Germantown, MD ยท On-site

$20 - $22/hr

... CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 ... We're proud of the impact we make and just last year, we supported 887 discovery projects , 1,100 ...

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Showing results 1-20

Project Manager Cdmo information

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 does a project manager at a pharmaceutical company do?

A project manager at a pharmaceutical company oversees the planning, execution, and completion of drug development and clinical trial projects. They coordinate teams, manage budgets, ensure regulatory compliance, and track project timelines using tools like Gantt charts and project management software. Their role ensures projects meet scientific, regulatory, and business objectives efficiently.

What are the key skills and qualifications needed to thrive as a Project Manager in a CDMO (Contract Development and Manufacturing Organization), 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 is the highest paying project manager?

The highest paying project managers are often those working in industries like technology, finance, or pharmaceuticals, with senior roles such as Program Manager or Portfolio Manager earning top salaries. Certifications like PMP and experience managing large, complex projects can also contribute to higher compensation, especially in regions with high demand for project management expertise.

Can I make 100k as a project manager?

Project managers, especially in the pharmaceutical or biotech industries, can earn $100,000 or more annually depending on experience, location, and certifications like PMP. Senior project managers or those working in high-demand sectors often have higher earning potential, with salaries influenced by project complexity and company size.

What is the highest paying job in pharmaceuticals?

In the pharmaceutical industry, senior roles such as Vice President of Research and Development or Chief Scientific Officer tend to be the highest paying positions, often earning six-figure salaries. Project Managers in CDMO companies with extensive experience and advanced certifications can also earn high compensation, especially when overseeing large-scale projects or managing multiple teams.
What are popular job titles related to Project Manager Cdmo jobs in Washington? For Project Manager Cdmo jobs in Washington, the most frequently searched job titles are:
What cities in Washington are hiring for Project Manager Cdmo jobs? Cities in Washington with the most Project Manager Cdmo job openings:
GMP Senior Project Manager

GMP Senior Project Manager

CAMRIS

Silver Spring, MD โ€ข On-site

$110K - $130K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago


Job description

Overview:

We are seeking a GMP Senior Project Manager to support the Pilot Bioproduction Facility (PBF) at the Walter Reed Army Institute of Research (WRAIR) in Silver Spring, Maryland.

PBF is a one-of-a-kind cGMP-compliant pharmaceutical manufacturing facility engaging in next-generation development for cutting-edge companies and government agencies. The professionals at PBF are engaging in trailblazing endeavors every day. Most exciting, the end products vary, so every year brings multiple opportunities for professional enrichment in original projects.

CAMRIS International, LLC, is a dynamic medical research and development firm that achieves innovative solutions to health and development challenges through high-quality, cost-effective programs and research management services. We combine our proven systems with today's most effective, evidence-based best practices. Our core practice areas include vaccine research, development, and production; microbiology and infectious disease research; biodefense; clinical research; global health security; and HIV/AIDS programs.

Our employees enjoy a collegial environment where individual contributions matter at all levels. At CAMRIS, you will notably improve the lives of people at home and abroad.

Responsibilities:

  • Solution project challenges with multi-disciplinary teams tracking and reporting metrics.
  • Manage project actuals vs. forecast and update status with program leadership.
  • Facilitate project team meetings, including scheduling, planning, and tracking.
  • Experience scheduling and executing GMP equipment design, testing and qualification.
  • Project planning and project lifecycle management from conception to completion.
  • Track qualification and operational readiness of equipment and systems, as necessary.
  • Leverage dependency matrices, diagrams, and gap assessments to define project scope.
  • Communicate and coordinate with PBF stakeholders to define scope and budget.
  • Grow and maintain relationships with WRAIR staff, customers, and vendors.
  • Organize and participate in customer and potential customer visits.
  • Manage project submittals, change control processes and project management artifacts.
  • Actively communicate customer project and facility constraints.
  • Evaluate schedule constraints, risk, and feasibility of performing CDMO projects.
  • Assist managers with subcontractor schedule development and maintenance.
  • Support shutdown planning and execution and update capacity utilization metrics.
  • Optimize and scale the Project Management function as capacity grows.
  • Perform other duties as assigned.

Qualifications:

Required

  • BS/BA in business, engineering, life sciences, or a related field and 10 years of biologics development or manufacturing industry experience, or an equivalent combination of education and credentials.
  • MS Project proficiency, including resource planning.
  • MS Excel, MS Word, MS SharePoint, and MS Teams familiarity.
  • Familiarity with implementing operational excellence.
  • Excellent written and verbal communication skills.
  • Must be currently eligible to work in the United States without visa sponsorship and have lived in the United States for three of the past five years if a non-US citizen.

Preferred

  • PMP and/or earned value training.
  • Knowledge of GMP, EU, FDA, ISPE guidance as it applies to multi-modal pharmaceutical manufacturing.
  • Biologics experience in development, manufacturing, or engineering.
  • Experience with cost analysis and finance.
  • CDMO project management experience.
  • Capital project management experience.
  • SmartSheet experience.
  • Leadership experience.

Physical Requirements, Workplace Hazards and Conditions, and PPE and Chemical Requirements:

The physical requirements, workplace hazards and conditions, and PPE and chemical requirements described here are representative of those that a candidate must meet to perform the essential functions of this job. Reasonable accommodation may be provided to enable individuals with disabilities to perform essential job functions.

Physical Demands

  • Constantly conduct sedentary work that primarily involves sitting/standing.
  • Occasionally conduct light work that includes moving objects up to 20 pounds.
  • Occasionally push or pull less than 25 pounds.
  • Occasionally reach above shoulder level.
  • Constantly use both hands.
  • Occasionally stand or walk for more than 25 minutes.
  • Occasionally kneel, squat, or stoop.
  • Constantly have clear vision (near and/or far), depth perception, peripheral vision, and/or visual acuity.

Physical Activities

  • Occasionally move about to accomplish tasks or move from one worksite to another.
  • Constantly communicate with others to exchange information.
  • Constantly assess the accuracy, neatness, and thoroughness of the work assigned.

Environmental Conditions

  • Constantly work in environments where no adverse environmental conditions are expected.

PPE and Chemical Requirements

  • Rarely wear PPE including but not limited to gloves, face shields/goggles, safety glasses, and safety shoes.
  • Rarely wear a lab coat.
  • Rarely wear a clean room uniform.
  • Rarely wear a disposable dust/surgical mask.

Please submit your resume online at www.CAMRIS.com. CAMRIS is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran status, disability status, or any other characteristic protected by any applicable federal, state, or local law.

CAMRIS offers a comprehensive benefits package, including medical, dental, and vision insurance for individuals and families, FSAs, HSA, life and AD&D insurance, short- and long-term disability, legal services, voluntary hospital indemnity, critical illness and accident insurances, EAP, pet insurance, 401(k) with employer match and Roth option, tuition and professional reimbursement, public transportation support in the DMV area, a referral bonus program, vacation with tenure-based increases, PTO, 11 paid holidays, paid bonding leave, and paid supplemental short-term disability.


Employment is contingent upon successful completion of a Public Trust-level background check, a requirement for this position under an active federal contract. The background check process may include, but is not limited to the following: (1) contacting your professional references; (2) verification of previous employment, education and credentials; (3) a criminal background check; (4) use/abuse of federally-controlled substances; and (5) a department of motor vehicle check. Candidates must be prepared to fully-complete any required background check questionnaire during initial onboarding.


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About CAMRIS

Sourced by ZipRecruiter

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

Bethesda, MD, US

Year founded

2003

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