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Project Manager - Medical Devices, cGMP

Eingestellt von Sentinel IT LLP

Gesuchte Skills: Support, Client

Projektbeschreibung

Project Manager - Medical Devices, cGMP - RELEVANT EXPERIENCE ONLY PLEASE

IMPORTANT

Please note that although this is a Project Manager position, specific experience in the Pharmaceutical experience is essential. Specific experience with Medical Devices is highly desirable.

Superb, global Pharma client require a Project Manager with prior Pharma experience for a long-term contract supporting the PMO with multiple project streams.

Description:

Essential Duties & Responsibilities

* Provides analytical support to the Project Management Office under minimal supervision.
* Proactively participates in processes and makes recommendations for system refinements within the Project Management Office.
* Support Planning Sessions as documentation lead and/or work stream lead.
* Participates in the evaluation and feasibility process for potential projects.
* Provides clear direction on project requirements to meet expectations of external customers and business stakeholders.
* Interacts through program and/or project updates and reviews with all levels of management.
* Drives implementation of projects by establishing strategy, schedules, budgets, and financial analysis.
* Drives use of Project Management Methodology throughout projects.
* Approves team deliverables for project completion.

Risk Management:

* Leads team in risk management approaches and systems.
* Responsible for making decisions regarding the appropriate risk when there is substantial project or program impact.
Administration:
* Ensures appropriate linkages of this information to the project prioritization and/or portfolio process.
* Maximizes business results through continuous improvement in organization's ability to execute projects and programs from initiation to completion and production scale-up.
* Owning Box site, tracking and execution of scope and financial deliverables and associated reporting. Finance Management
* Eliminates or minimizes barriers to progress.
* Anticipates potential conflict situations, identifies and acts on proactive solutions.
* May perform other duties as assigned.

Communication:

* Weekly and monthly SharePoint updates of Initiative and Milestone Status
* Participation, including presenting updates/escalated items and fielding questions, in the program meeting
* Escalation of issues, risks, and changes via communication mechanisms
* Utilizing and enhancing standard reporting and communication tools to ensure appropriate and timely communication and reporting from multiple projects.
* Meeting participation/facilitation
* Knowledge of cGMP manufacturing.
* Knowledge of Quality Systems
* Good interpersonal skills and be able to work effectively and efficiently in a team environment.
* Must have ability to lead cross-functional teams.
* Must display eagerness to learn and continuously improve.

Education and/or Experience:

* 4 to 7 years project management experience and with a track record of multi-site, global or enterprise-wide programs, preferably in the medical products industry

Please apply now for more details!

Projektdetails

  • Einsatzort:

    Brussel, Belgien

  • Projektbeginn:

    asap

  • Projektdauer:

    Keine Angabe

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Sentinel IT LLP