Project Manager with Cell Therapy or Pharma Background

  • Montek System
  • Seattle, Washington
  • Full Time
Project Manager with Cell Therapy or Pharma Background

Top Skills:

- Experience in the Biotech/Cell Therapy industry Preferred / Familiarity with end-to-end CMC drug development with an understanding of critical milestones and typical bottlenecks preferred.

- PMP Experience Preferred

- Experience with tools: Smartsheets, Tableau, and MS Projects

- Strong organizational skills, ability to multi-task and work in a dynamic, fast paced environment.

The Project Manager is closely partnered with the GMS&T Leader to enable effective execution of strategy and plans. The scope of responsibilities of the Project Manager fall into 4 general categories which flex across all drug modalities, disease areas and stages of development.

1. Cross-functional Project Management to ensure integrated execution of LCM strategy and communication

2. Project Timeline Management and timeline scenario planning

3. Assist with Gaps Analysis and Risks Management

4. Ensure connectivity with key partners on critical actions, timelines etc

Primary Responsibilities:

In partnership with GMS&T Team Leader, manage multiple commercial LCM program assignments (actual number determined by level of project complexity and candidate experience) and drive execution of integrated program strategy

Develop detailed project plan that is aligned with the overall strategy. Work collaboratively with the CTO team leaders and cross functional teams to track all project milestones

Facilitate pertinent scenario planning to address changing business/clinic needs. Gather stakeholder input, evaluate, collate, manage and communicate implications and adjustments to the overall plan

Manage all meeting logistics including the creation of clear, concise minutes

Partner with the GM&ST Leader to facilitate the management and communication of program risks and mitigation strategies

Leverage portfolio and program management tools to track program execution, milestones, risks, and long range planning to ensure appropriate communication to team members and management. Examples include MS Project Server, ePlan, PSI CMC database, OnePager Pro, DOI Tool, Right First Time Scorecard, Operational Risk Management

Coordinate and ensure appropriate allocation of DS and API materials for non-clinical use

Experience / Qualifications:

Bachelor's degree in engineering or relevant scientific discipline with at least 5 years of relevant experience / Masters degree with a minimum of 2-6 years of relevant experience

Highly motivated self-starter that works well both in teams as well as independently

Strong project management, business process management, and optimization skills

Familiarity with end-to-end CMC drug development with an understanding of critical milestones and typical bottlenecks preferred

Strong organizational skills, ability to multi-task and work in a dynamic, fast paced environment.

Demonstrated ability to accomplish results and meet deadlines and commitments

Strong interpersonal and communications skills, both oral a written

Demonstrated proficiency in MS Project, PowerPoint, Excel and Word

Demonstrated ability to build relationships, influence, negotiate, and drive organizational engagement

Experience developing and/or managing program management tools to forecast budgets, timelines and resources preferred

PMP Preferred

Employers have access to artificial intelligence language tools (AI) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

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Dice Id:

91093412

Position Id:

8692527
Job ID: 484868542
Originally Posted on: 7/11/2025

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