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Engineering Project Manager

  • Gdańsk, pomorskie
  • Kierownik
  • 03.10.2018

    Pracodawca ma prawo zakończyć rekrutację we wcześniejszym terminie.

    if you want to work

    in one of the
    most modern biotechnology
    centres in Europe
     
    in place where
    profesionals
    from all over
    the world work
    on the highest-quality equipoment
     
    in the production
    of biotechnological
    drugs, which dive
    access to effective
    therapy to more
    patients
     
    in a company that will
    dive you stable
    employment competetive
    remuneration attracive
    benefits and the
    opportunity to participate
    in training at home
    and abroad
     
    Currently we’re looking for
    1
    Engineering Project Manager

    Join “start-up” Biologics division with strong international and local team at site!

     

     
    We are waiting just for you!


     
     

    What will you do?

    • Manage and communicate project definition, milestones, schedules, and project statuses
    • Evaluate and approve changes that substantially impact scope, budget or schedule of the project
    • Report and present status and schedule of the project to senior management
    • Define tasks and required resources
    • Assign and manage project team
    • Allocate project resources
    • Track deliverables
    • Lead meetings and document action items and their progress
    • Coordinate technical discussions with Engineering team
    • Collaborate with all teams of Polpharma Biologic.

    What do we offer?

    • Employment contract  with opportunity to help shape the success of a leading private pharmaceutical company
    • Competitive salary, performance-related bonus and attractive fringe benefits
    • Relocation package
    • Joining “start-up” Biologics division with strong international and local team at site.
     

    What do we expect?

    • 3-5 years of experience in a similar position, i.e. experience in Engineering Project Management within pharmaceutical industry
    • Knowledge of cGMP and FDA requirements
    • Strong track record of on-time project delivery and managing entire project life-cycle
    • Higher technical education
    • Knowledge of MS Office, especially Microsoft Project
    • Fluent English (written and spoken)
    • Excellent work organization and result orientation; ability to plan, schedule and monitor complex technical projects, their implementation within set time and given budget
    • Ability to report potential problems related to project and interested parties
    • Full awareness of financial status and degree of implementation regarding schedule of allocated projects
    • Ability to identify and reduce risk (Risk Management in the project)
    • Excellent communication and responsiveness skills.