OBS! Ansökningsperioden för denna annonsen har
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Arbetsbeskrivning
Do you want to lead and drive projects from start to finish? Do you have substantial experience in the Pharma/OTC Industry and are ready for a new challenge? Then, the role of Project Manager LCM with our client in Helsingborg could be the next step in your career. Seize the opportunity to be a key player in an exciting project and apply today!
Location: Helsingborg
Start: January 2024
Assignment Duration: 12 months
Additional Information: Consulting assignment where you will be employed by Jefferson Wells and work with our client.
Job Description:
In the role of Project Manager LCM, you are expected to lead and execute essential project stages such as project definition, due diligence, and gap analysis. Additionally, your responsibility includes creating a detailed project plan that guides the entire project.
You will be in charge of effectively managing cross-functional teams through each phase of the project, ensuring smooth coordination of all activities, and contributing to the project's progress.
Tasks and Responsibilities:
* Qualify new raw material sites.
* Monitor and balance risks and opportunities.
* Prepare budgets and track costs using necessary tools.
* Communicate effectively with senior management.
* Lead processes and governance for the smooth evaluation and approval of projects within EMEA.
The Ideal Candidate:
In the role of Project Manager LCM, having substantial experience in the Pharma/OTC Industry is crucial, forming a solid foundation for successfully leading and driving the project. Additionally, you need to be business-oriented and possess knowledge of project-related finances for effective and sustainable project planning.
You should also have the ability to manage team dynamics, especially within virtual teams, and strong planning and organizational skills.
Qualifications:
* Master's/bachelor's degree in supply chain, project management, business administration, or pharmaceutical sciences.
* Minimum 8 years of experience in the Pharma/OTC Industry.
* PMP certification in project management.
* Experience in Validation, Regulatory, or Quality Assurance is considered advantageous.
* Fluent in English, both oral and written.
* Proficient in MS Project, with good PowerPoint and Excel skills.
Application:
Warmly welcome your application by registering your CV. Selection is ongoing, so don't hesitate to submit your application. We do not accept applications via email.