• Integrate capacity modeling capabilities into our software platform. • Act as an internal subject matter expert and implement ideal modeling assumptions. • Work with external partners to ensure high-quality data. • Provide expertise in responses to user questions and methodology discussions during the sales process. • Generate ideas to improve the product to better fit customer needs. • Work on economic modeling projects related to transmission congestion analysis, LMP basis risk, energy curtailment risk, LMP price forecasting, and economic benefit studies. • Collaborate with software developers to integrate models into our cloud ecosystem. • Assist in technical sales calls with potential new clients. • Conduct analysis to verify and improve outputs from external consultants. • Manage client engagements and ongoing relationships, presenting study results to key stakeholders.

• Evaluate and quantify the performance of operating projects in Terra-Gen portfolio. • Build and utilize tools to assess and report on plant performance. • Interface with Operations, Asset Management, Finance, and Development teams. • Develop and implement tools/models to evaluate, monitor, and report on performance KPI’s across the Terra-Gen portfolio. • Oversee the resolution process to correct performance engineering issues. • Support Terra-Gen O&M teams, providing actionable items and gathering feedback from the field. • Work closely with TG development and engineering teams.

• Serve as a clinical and technical subject matter expert within Quality Assurance and provides advanced clinical expertise to assess device performance concerns, determine regulatory reportability, identify root causes, and support risk management activities. • Play a key role in ensuring regulatory compliance, identifying safety signals, and supporting product quality and patient safety. • Collaborate cross-functionally with Quality, Regulatory Affairs, R&D, Manufacturing, and Clinical teams to evaluate complaints, interpret clinical and device data, and ensure accurate, compliant complaint handling in accordance with FDA, EU MDR, and other global regulatory requirements. • Partner closely with Field Clinical and Technical teams to ensure timely reporting of device-related issues and collection of complete, high-quality information to support thorough complaint investigation and evaluation. • Act as senior clinical and technical SME for complaint investigations involving implantable medical devices including assessment of device performance and patient outcomes. • Support Quality Leadership in identifying emerging product performance trends, reliability concerns, and potential risk signals through complaint trending and data analysis. • Perform global regulatory reportability assessments in accordance with applicable regulations, including FDA Medical Device Reporting (21 CFR 803), EU MDR Vigilance Reporting, TGA, PMDA, MHRA, and other international regulatory requirements. • Provide clinical and technical input to support regulatory submissions, responses to Competent Authority inquiries, and vigilance reporting activities. • Participate in cross-functional reviews of complaint trends, product performance, reliability, and patient safety. • Support internal audits, external audits, and regulatory inspections related to complaint handling, vigilance reporting, and post-market surveillance activities. • Drive continuous improvement of post-market surveillance (PMS) and complaint handling processes.

• Support complex equipment projects ensuring completion accurately and on-time • Manage project Profit and Loss (P&L) and customer satisfaction • Work with branch administrations to manage backlog execution, schedule, and forecast execution • Coordinate factory equipment order process to ensure compliance with contract documents • Ensure project documentation is compliant with contract requirements