Leads scouting, vetting, and commercialization of frontier energy technologies to power AI infrastructure. Drives incubation from concept to scalable deployment, including technoeconomic modeling, partnerships, pilots, and cross-functional execution with high agency in ambiguous environments.
Salary not listed
On-siteOther
About the role
What You'll Be Working On
Building and maintaining a Crusoe-specific market map of energy technologies, market structures, and regulatory pathways that can unlock speed and advantage
Sourcing and conducting due diligence of opportunities aligned to Crusoe’s power and infrastructure roadmap, including shadowing strategic finance partners’ deal pipeline meetings
Converting frontier insights into actionable bets with clear diligence plans, decision memos, pilot project designs, and scale pathways
Incubating technologies and partnerships from concept to deployable projects
Partnering with Crusoe’s commercial, operational and legal teams to structure and negotiate agreements that create long-term strategic advantages for Crusoe
Driving cross-functional projects across engineering, business development, finance, legal, data center execution, and public affairs
Creating energy technology-focused partnerships with academic institutions, government labs or similar research institutions
Publishing high-signal thought leadership pieces that reinforce Crusoe’s positioning as a market leader
What You'll Bring to the Team
Position Crusoe at the forefront of energy-first AI infrastructure development
Define and continuously refine Crusoe’s energy innovation and commercialization thesis tied to the company’s compute roadmap and siting strategies
Translate strategy into execution by establishing clear priorities, decision criteria, and “kill/scale” gates
Produce board- and exec-ready materials that drive decision velocity
Map the frontier of energy technologies and develop campus-level technoeconomic models incorporating future technologies
Maintain an active view across generation, storage, fuels, grid-edge solutions, interconnection enablers, and enabling software
Evaluate options with execution realism: technological feasibility, supply chain, permitting, safety, operability, reliability, cost, timeline, and bankability
Build a living “Frontier Map” and keep it operationally relevant to Crusoe’s near-term and medium-term project pipeline
Develop campus-level technoeconomic models to stress-test future generation designs across technologies, electrical architecture, and build-out timing. The model will translate design choices into $/kW-month, delivered $/MWh, uptime risk, and time-to-energize
Incubate and de-risk new technologies into deployable pathways
Stand up a repeatable incubation motion: source → diligence → partner → pilot → scale or terminate
Design pilots tied to real sites and real constraints, with measurable outcomes and clear ownership
Build partner ecosystems across developers, OEMs, EPCs, utilities, ISOs/RTOs, financiers, and key suppliers
Recommend build vs. buy vs. partner vs. invest with clear rationale and quantified tradeoffs
Drive deal flow for Crusoe’s Corporate Development team
Source early-stage opportunities aligned to Crusoe’s roadmap and competitive advantage
Join Crusoe’s strategic finance partners’ (VCs, etc.) to vet their deal pipelines for possible fit with Crusoe
Lead diligence across technical, market, regulatory, and commercial dimensions
Produce investment memos and recommendations; support term negotiation alongside legal and the investment committee
Director of Regulatory Affairs and Quality Assurance
EightsleepSan Francisco, CA
Lead risk management, regulatory submissions (FDA 510(k), De Novo), and quality systems (ISO 13485/14971) for medical device sleep technology. Requires 8+ years in medical device QA/RA, successful FDA clearances, and cross-functional leadership with R&D and Clinical teams.
Salary not listed
On-site8+ YOEOther
Director of Medical Operations
EightsleepSan Francisco, CA
Lead medical operations for sleep fitness medical devices at Eight Sleep. Implement manufacturing controls, oversee design verification/validation testing, FDA clearances, and risk management while collaborating with R&D, QA/RA, and clinical teams. Requires 8+ years medical device operations experience and successful FDA track record.
Salary not listed
On-site8+ YOEOther
Director, Investor Relations
AnthropicSan Francisco, CA
Build and lead Anthropic's investor relations program as primary contact for the investment community. Synthesize financial, strategic, and AI developments into clear narratives; advise leadership on investor sentiment while building financial models and relationships.
425k – 600k/yr
Hybrid8+ YOEOther
Director, AI & Business Automation
IllumioSunnyvale, CA
Lead enterprise-wide AI transformation as direct report to the CIO. Define AI strategy, architect Agentic AI and hyper-automation workflows, establish governance, drive business process modernization across functions, and deliver measurable ROI.
227k – 272k/yr
On-site15+ YOEOther
Associate Director, GMP Quality
Formation BioBoston, MA +1
The Associate Director, GMP Quality Assurance ensures compliance for Formation Bio's biologics portfolio by reviewing GMP documents, conducting batch releases, leading investigations, auditing CDMOs, and supporting regulatory inspections. Requires 10+ years GMP QA experience in large-molecule manufacturing, bachelor's in a scientific field, and hands-on quality leadership in a dynamic environment.