Senior Project Manager - Engineering & Automation

Regeneron; City of Troy (NY); On-site; USD 141,400 - 231,000; Full time

Job summary

Regeneron is seeking a Senior Project Manager—Engineering & Automation to lead complex cGMP technology implementations within our Industrial Operation and Product Supply team in Troy, NY. You will apply project management principles to deliver value quickly, coordinate resources, and manage stakeholder expectations while upholding quality and compliance.

Responsibilities include developing automated dashboards to report project performance, guiding SDLC for computerized assets, mitigating

Qualifications

• BS/BA in Science/Engineering or related technical field.
• 10+ years of experience in Engineering, Automation, or Information Technology.
• Direct experience in pharmaceutical/biopharmaceutical manufacturing with cGMP.
• Strong knowledge of Change Management in a GxP environment.

Responsibilities

• Oversee complex, interdependent cGMP technology implementations.
• Develop automated dashboards to report project performance using KPIs.
• Lead teams, align stakeholders, and resolve conflicts to improve speed-to-value.
• Ensure SDLC processes are applied to computerized assets and deliverables.

Skills

Project management

Leadership

Data analytics

Communication

GxP knowledge

Change management

Portfolio management

Education

BS/BA in Science or Engineering

Tools

MS Project

Azure DevOps

Jira

Job description

Senior Project Manager – Engineering & Automation

We are looking for an experienced Project Manager to join our growing team. 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.

When & Where

• Monday‑Friday 8:00 am‑4:30 pm
• Troy, NY

Discover Your Role

• 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, streamline stakeholder communication, and resolve 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.

This Role Requires

• BS/BA in Science/Engineering or a related technical field along with 10+ years of relevant experience in an Engineering, Automation, or Information Technology setting.
• Direct experience in a pharmaceutical or biopharmaceutical manufacturing facility, with a high level of proficiency in project management within a portfolio management framework, as well as 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.
• Knowledge and experience with the design, development, configuration, and implementation of computerized equipment and systems for cGMP use is preferred.

Salary Range (Annual)

$141,400.00 – $231,000.00

Benefits

• Annual bonuses or other incentive plans
• Equity awards
• Pension or retirement benefits
• 401(k) company match
• Health and wellness programs
• Fitness centers
• Insurance benefits (medical, dental, vision, life, disability)
• Paid time off
• Family support benefits

Equal Opportunity Employer

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.