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Us_Project Manager I #: 23-02626
Company | HireTalent - Diversity Staffing & Recruiting Firm |
Address | South San Francisco, CA, United States |
Employment type | CONTRACTOR |
Salary | |
Category | IT Services and IT Consulting,Financial Services,Accounting |
Expires | 2023-06-01 |
Posted at | 1 year ago |
Job Duration: 6 Months on W2
Job Summary
The Process Validation Project Manager (PV PM) role will provide support to Technical Development Teams (TDTs) on Process Validation (PV) including project and portfolio analyses and communication of key insights to inform decision-making. He/She/They will work closely with PV stakeholders to plan, maintain, and manage all PV deliverables. The role will be in the Pharma Technical Development Project and Portfolio Management PTDM).
Job Responsibilities
- Support the TDTs and ensure on-time Market Applications (MAs) by developing and maintaining PV project schedules and dashboards to track progress.
- Apply drug/CMC process development knowledge and project management expertise to manage PV deliverables for multiple projects through MA filing and Pre Licensure Inspection (PLI).
- Provide expertise and guidance to TDTs on PV at project level including continuous improvement of business processes and tools analyses and communication of key portfolio insights to inform decision-making.
- Act as a valuable member of the overall project team system (e.g. shares best practices and lessons learned).
- Lead regular meetings with PV leads to ensure PV studies are on track and keep all relevant stakeholders including the Technical Development Leader (TDL) updated on PV project status, key risks and issues.
- BS/BA degree in scientific field
- 2+ years drug development project management and process validation experience is preferred
- 2+ years in the pharmaceutical/biotech industry
- Experience and knowledge with Smartsheet, Tableau, and other reporting and tracking tools
- Ability to manage cross-functional teams and development projects and to apply project management skills, methodologies and tools
- Knowledge and experience with end-to end CMC process development; relevant process validation, regulatory, quality and cGMP expertise is preferred
- Strong collaborative and relationship-building skills; demonstrated ability to effectively partner and influence internal and external stakeholders
- Excellent verbal and written communication skills; must be able to effectively communicate/articulate strategy and deliverables to team members and senior management
- Knowledge of the drug development process
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