Senior Project Manager - Engineering & Automation

Regeneron Pharmaceuticals

3d•$141,400 - $231,000•Onsite

About The Position

The Senior Project Manager—Engineering & Automation will apply technical skills and resources to deliver impact quickly, without compromising quality, and manage stakeholder expectations to ensure technological development & implementation projects that bring value aligned with cGMP procedural requirements and strategic goals of Regeneron’s Industrial Operation and Product Supply organization. You will efficiently allocate resources and monitor progress by tracking key performance indicators against specific business processes. Capitalize on technical background and knowledge of project management principles to deliver strategic value through oversight of complex, interdependent cGMP technology and equipment implementations. Ensure key technical resources are in place to achieve project deliverables, optimizing them with iterative, feedback-driven processes. Lead teams, streamlining stakeholder communication, and resolving conflicts with approaches tailored to improve speed-to-value. Ensure SDLC processes and implementations are applied to desired project outcomes. Develop automated dashboards to report project performance, tracked by timely, strategic goal-oriented key performance indicator assessment. Minimize project complexity through risk identification and mitigation tactics, efficiently allocating resources, and monitoring progress by tracking key performance indicators. Use data analytics and supportive AI to forecast business impact and streamline decision-making.

Requirements

BS/BA in Science/Engineering or a related technical field
10+ years of relevant experience in an Engineering, Automation, or Information Technology setting
Direct experience in a pharmaceutical or biopharmaceutical manufacturing facility
High level of proficiency in project management within a portfolio management framework
Experience with computerized system procurement, design, installation, and support in a cGMP industrial setting
Strong knowledge and experience of Change Management in a GxP environment
Detailed understanding of bioprocessing equipment design and GxP software quality system principles, with a focus on data integrity
Broad business acumen and understanding of how to apply system development lifecycle concepts to computerized assets implemented globally for qualified use in a GxP environment
Advanced portfolio/program/project management experience
Ability to develop & publish schedules, dashboards, reports, and other project documents using project planning tools such as MS Project, Azure DevOps, Jira, etc.
Excellent communication (verbal and written), analytical and problem-solving skills, demonstrating creative and independent reasoning to navigate scope, time, and cost constraints, assuring quality deliverables.

Nice To Haves

Knowledge and experience with the design, development, configuration, and implementation of computerized equipment and systems for cGMP use is preferred.

Responsibilities

Deliver strategic value through oversight of complex, interdependent cGMP technology and equipment implementations.
Ensure key technical resources are in place to achieve project deliverables, optimizing them with iterative, feedback-driven processes.
Lead teams, streamlining stakeholder communication, and resolving conflicts with approaches tailored to improve speed-to-value.
Ensure SDLC processes and implementations are applied to desired project outcomes.
Develop automated dashboards to report project performance, tracked by timely, strategic goal-oriented key performance indicator assessment.
Minimize project complexity through risk identification and mitigation tactics, efficiently allocating resources, and monitoring progress by tracking key performance indicators.
Use data analytics and supportive AI to forecast business impact and streamline decision-making.