ZipRecruiter

Log In

1

Manager Cdmo Jobs in Washington (NOW HIRING)

CAMRIS

GMP Senior Project Manager

Silver Spring, MD · 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 ...

CAMRIS

GMP Senior Project Manager

Silver Spring, MD · 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 ...

CAMRIS

GMP Project Manager

Silver Spring, MD · 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 ...

CAMRIS

GMP Project Manager

Silver Spring, MD · 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 ...

next page

Showing results 1-20

All JobsCdmo JobsManager Cdmo JobsManager Cdmo Jobs in Washington

Manager Cdmo information

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.

What are the most commonly searched types of Cdmo jobs in Washington? The most popular types of Cdmo jobs in Washington are:
What are popular job titles related to Manager Cdmo jobs in Washington? For Manager Cdmo jobs in Washington, the most frequently searched job titles are:
What job categories do people searching Manager Cdmo jobs in Washington look for? The top searched job categories for Manager Cdmo jobs in Washington are:
What cities in Washington are hiring for Manager Cdmo jobs? Cities in Washington with the most Manager Cdmo job openings:
Manager Cdmo jobs near you

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

uBriGene Biosciences International Co

Germantown, MD • On-site

$60K - $100K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

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.

Apply