Validation - Project Manager

Job Description: Location: SeattleDexter WA*Hybrid
Top Skills:
Experience in the Biotech/Cell Therapy industry Preferred
PMP Experience Preferred
Experience with Smartsheets Tableau and MS Projects
Strong organizational skills ability to multitask 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. Crossfunctional 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 nonclinical use

Experience / Qualifications:
Bachelors degree in engineering or relevant scientific discipline with at least 5 years of relevant experience / Masters degree with a minimum of 26 years of relevant experience
Highly motivated selfstarter that works well both in teams as well as independently
Strong project management business process management and optimization skills
Familiarity with endtoend CMC drug development with an understanding of critical milestones and typical bottlenecks preferred
Strong organizational skills ability to multitask 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
Additional Sills: