Assoc Dir, CMC Project and Portfolio Management

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Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

The Associate Director will be a key member of the Project Management Office within Biologics CMC located in West Chester, PA.  We are seeking a highly experienced project manager to build and develop the project team and has the ability to collaborate with, and influence internal/external stakeholders, and play a major role in the overall success of the organization.

 

 

Responsibilities include managing:

Projects, tech transfer, goods inventory, risk assessment and mitigation (FMEA), international markets deployment, operational and CapEx budgets, and development of a project management toolbox (Gantt charts, RACI charts, risk analysis and mitigation, budgets, detailed schedules and timelines). 

 

Other duties:

⦁    Lead projects from requirements definition through deployment, identifying schedules, scopes, budget estimations, and project implementation plans, including risk mitigation.

⦁    Analyze project progress and, when necessary, adapt scope, timelines, and costs to ensure that project team adheres to project requirements

 

What you will bring to the role:

• Demonstrated experience in the development and deployment of a project management toolbox
• Expert working knowledge of project management fundamentals
• The ability to read, interpret, and follow SOP's, and other procedures
• Strong understanding of cGMPs as applicable to biologic operations
• Excellent oral and written communication skills
• Strong organization and problem-solving skills
• Experience in developing project management tools

 

Qualifications

 

⦁    15+ years of project management or relevant experience within the cGMP biopharmaceutical industry

⦁    A Bachelor's degree in a life science-related field.

 

 

Preferred Qualifications:

⦁    20+ years of project management or relevant experience within the cGMP biopharmaceutical industry

⦁    PMP certification

Function

Sub Function

Reports To

In process of validation

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