Job Description :
6+ years of relevant experience and a BA or BS or a MS or MBA; and/or 8-10+ years of relevant experience working association with Quality in Pharmaceutical, Biotechnology, or Medical Device Industry; and/or 4+ years of experience working with project teams and/or in cross-functional project management activities.

Provide project management support Services for Client’s Quality Organization in Foster, City, CA that will include the following:

Work with the Gilead Quality Organization on Operational Excellence initiatives/projects.

Manage Organizational and/or Functional Quality Plan initiative to ensure continuous progress towards achieving goals and objectives through the completion of defined activities.

Manage team meeting scheduling, monitoring completion of action items, mitigation of identified risks and communication of roadblocks.

Manage coordination of collaboration between cross-functional resources for completion of selected Clinical Lot Release activities.

Ensure compliance with Regulatory Guidance documents and cGMP requirements.

Manage and communicate overall project status updated to the Project Management Office and Quality Leadership.

Coordinate and support client-wide forums chaired by Quality Leadership.

Build timelines, work breakdown structures, following up with staff on the completion of their tasks,

Use PowerPoint, MS Project, or Excel to create concise presentations for Leadership on status of project,

Act as voice of senior management for guidance of projects and initiatives at the direction of client.
             

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