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Sr. Director - Engineering (Automation, Process, Maintenance)

Scorpion Therapeutics, Virginia, MN, United States


Role Summary Sr. Director - Engineering (Automation, Process, Maintenance) at Lilly's Goochland County, Virginia manufacturing site. Lead the site’s process-facing engineering functions—including process engineering, automation, and maintenance—to ensure startup readiness and long-term manufacturing goals. Provide administrative and technical leadership for engineering operations as a member of the Site Lead Team shaping strategic direction and capability.

Responsibilities Pre-Startup & Startup Phase

Organizational Development: Collaborate with the Site Lead Team to build a capable, inclusive, and resilient organization focused on safety, quality, and operational excellence.

Functional Strategy: Define priorities and roadmap for process engineering, automation, and maintenance. Develop systems and processes by leveraging internal expertise and external best practices.

Safety Leadership: Actively contribute to the site HSE Lead Team to ensure safety is embedded throughout project delivery and startup.

Project Support: Act as end user for process equipment—providing input on design, commissioning, and startup plans to align with both project and long-term site goals.

Team Structure: Design and evolve the engineering organization to ensure the right resources and leadership are in place for GMP manufacturing.

System Readiness: Ensure qualified and safe states for equipment, processes, utilities, and facilities are established and maintained.

Corporate Alignment: Build strong technical relationships with corporate teams and champion strategic initiatives at the site level.

Post-Startup Phase

Ongoing Strategy Execution: Continue refining and executing the engineering roadmap, aligning functional goals with site priorities.

Compliance & Standards: Ensure adherence to corporate policies and standards across environmental, safety, and quality domains.

External Benchmarking: Maintain an outward focus to identify and apply best practices from across the industry and internal network.

Asset Management: Partner with Facilities Engineering to manage site investments—planning, prioritizing, and executing capital projects aligned with site objectives.

Operational Integrity: Ensure equipment remains in a qualified and safe state, and that maintenance is performed and documented to the highest standards.

Governance & Controls: Establish and maintain robust control systems to manage compliance and elevate issues appropriately.

Leadership Development: Cultivate future technical and managerial leaders for the site and potential global roles.

Qualifications

Required:

10+ years of experience in a leadership role managing teams within the pharmaceutical industry

Preferred:

Experience in API and aseptic manufacturing, including implementation of a Process Safety Management program.

Preferred:

Strong understanding of cGMPs and their application to manufacturing operations.

Preferred:

Proven ability to build effective relationships across all organizational levels—from site leadership to frontline teams.

Preferred:

Demonstrated success in leading projects from initiation to completion, meeting timelines, budgets, and performance standards.

Preferred:

Track record of developing and managing high-performing, engaged teams with a focus on safety, quality, and strong team culture.

Education

Bachelor's degree in an engineering discipline

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