Bausch Health

  • Director, Project Management - GI

    Location US-NJ-Bridgewater
    Job ID
    11869
    Category
    R&D
    Pos. Type
    Full Time
  • Overview

    Reporting to the Executive Director, Pharmaceutical Project Management, the Director of Project Manager will use the global PCPF (development process), allied systems & tools, to plan and manage/coordinate resources and activities related to new product development for Gastrointestinal pharmaceuticals. 

     

    This position resides in the Bridgewater, NJ office.

    Responsibilities

    • Champion and lead projects for GI pharmaceutical development and product improvement projects.
    • With team develops overall project plan and resource requirements.
    • May work under a Program Head in the identification, management and resolution of issues
    • May lead one or more sub-teams of a program, including specific indications
    • Contributes to the overall strategy, feasibility and supports the preparation of plans and presentations
    • Management of projects in compliance with defined process and procedures.
    • Management of project team members from the various other functional areas assigned to a specific program (includes team meetings, communications to teams and meeting minutes etc.).
    • Review and monitor program/project activities against definition, schedule and costs.
    • Prepare amended budget forecasts as required.
    • Deliver products to agreed timelines and budgets.
    • Communicate effectively with RD&E management and staff regarding the status of all activities.
    • Inform management in a timely manner of any problems which may result in a delay in project schedules so that appropriate action may be taken.
    • Publish monthly/quarterly project report summaries as required including product presentations to development committee and senior management.

    Qualifications

    • Bachelors/Masters degree in science required with 10 to 15 + years of GI related Project Management development experience.
    •  10 – 15 years in GI, Quality, Regulatory or Microbiology experience with specific experience in managing complex, highly technical R&D / Drug Development related activities also considered.
    • Prior training in project management.  PMI certification a plus.
    • Proven, hands-on, results-oriented manager with demonstrated leadership skills across functional lines and a participatory style of working effectively in a dynamic, team-oriented environment.
    • Ability to communicate and interact at all levels from senior management to staff level.
    • Ability to translate customer requirements into measurable design goals/input.
    • Competency in Microsoft Project, Word, PowerPoint & Excel.
    • Excellent verbal, written and electronic communication skills.
    • Therapeutic area experience in gastroenterology a requirement.
    • Proficiency in a foreign language (German, French) a plus.
    • Ability to travel, 7 – 10% overnight travel, domestic and international.

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