
10,000+ employees
💼 Consulting
📦 Logistics
🏭 Manufacturing
Consulting • Logistics • Manufacturing
GE Vernova is a leader in the energy sector with over 130 years of experience, dedicated to electrifying the world while decarbonizing it. The company offers a broad portfolio of energy solutions including gas, hydro, nuclear, and wind power technologies, aimed at providing reliable, affordable, and sustainable energy. With a strong focus on innovation, GE Vernova plays a significant role in reducing the carbon footprint of global power systems and supports the transition to net-zero emissions by 2030.
🔥 46 minutes ago
Improve your chances of getting an interview by checking your resume score before you apply.

10,000+ employees
💼 Consulting
📦 Logistics
🏭 Manufacturing
Consulting • Logistics • Manufacturing
GE Vernova is a leader in the energy sector with over 130 years of experience, dedicated to electrifying the world while decarbonizing it. The company offers a broad portfolio of energy solutions including gas, hydro, nuclear, and wind power technologies, aimed at providing reliable, affordable, and sustainable energy. With a strong focus on innovation, GE Vernova plays a significant role in reducing the carbon footprint of global power systems and supports the transition to net-zero emissions by 2030.
• Assess potential suppliers, conduct on-site audits, and execute supplier quality surveillance programs for new reactor projects • Define quality requirements and provide technical guidance to ensure adherence to engineering specifications • Oversee the disposition of non-conforming products • Partner with suppliers to implement defect-reduction strategies • Utilize corrective action processes to prevent future errors • Author and review technical quality documents, plans, and procedures • Maintain rigorous supplier quality performance records • Act as a technical liaison between purchasing, engineering, and suppliers • Ensure project requirements are met • Travel to supplier and customer sites for evaluations as required, up to 50%
• Associate’s degree from an accredited institution • Alternatively, a High School Diploma or GED with a minimum of 8 years of relevant professional experience • Minimum of 4 years in engineering, manufacturing, manufacturing support, or nuclear quality assurance • Proven understanding of quality control principles, methodologies, and quality assurance systems • Working knowledge of manufacturing processes and industrial standards • Proficiency in data analysis, performance tracking, and technical reporting to monitor supplier quality metrics • Exceptional verbal and written communication skills in English • Ability to manage competing priorities and multiple projects simultaneously • Ability and willingness to travel to supplier and customer sites as required, up to 50% • Access to U.S. export-controlled information requires authorization from the U.S. Government, if applicable • Must be legally authorized to work in the United States • Successful completion of a drug screen, as applicable • Desired: Bachelor’s degree in a Science or Engineering discipline • Desired: Active or prior certification as a Quality Lead Auditor • Desired: Minimum of 2 years of dedicated experience in a nuclear quality role • Desired: Understanding of 10CFR50 Appendix B, NQA-1, CSA N299, CSA N285, and ISO-9001 • Desired: Expertise in ASME Section IX and Section XI • Desired: Experience in NDE processes and complex welding troubleshooting • Desired: Proficiency in analog/digital control systems, pneumatic instrumentation, PLC programming, SCADA configuration, and safety lifecycle for high-integrity software-based systems • Desired: Familiarity with IEEE, IEC, IPC, NEMA, and ANSI standards • Desired: Experience performing rigorous inspections • Desired: Broad knowledge of the nuclear landscape • Desired: Proven Nuclear Safety Culture leadership • Desired: Exceptional ability to engage and influence senior leadership at supplier and regulatory organizations • Desired: Strong interpersonal skills and customer-focused, high-performance team orientation • Desired: Self-motivated, analytical problem-solving skills, and ability to thrive in changing environments • Desired: Willingness and ability to travel up to 50%
• Competitive compensation • Discretionary annual bonus • Medical, dental, vision, and prescription drug coverage • Health Coach from GE Vernova, a 24/7 nurse-based resource • Employee Assistance Program with 24/7 confidential assessment, counseling and referral services • GE Vernova Retirement Savings Plan • Tax-advantaged 401(k) savings opportunity with company matching contributions • Company retirement contributions • Access to Fidelity resources and financial planning consultants • Tuition assistance • Adoption assistance • Paid parental leave • Disability benefits • Life insurance • 12 paid holidays • Permissive time off • Professional development • Relocation assistance not provided
Apply Now🔥 4 hours ago
Medical complaint specialist reviewing escalated records and MQ tickets for Siemens Healthineers’ medical technology business. Supporting compliance, reporting, training, and process improvement.
🇺🇸 United States – Remote
💵 $65.2k - $89.7k / year
💰 $1.5M Grant on 2021-05
⏰ Full Time
🟡 Mid-level
🟠 Senior
🔥 8 hours ago
Quality Business Specialist leading insurance quality assurance, compliance, and corrective actions for Globe Life’s Family Heritage Division. Monitoring KPIs, investigating misconduct, and reporting to senior leadership.
🇺🇸 United States – Remote
💰 $250M Post-IPO Debt - Globe Life on 2024-08
⏰ Full Time
🟡 Mid-level
🟠 Senior
🕒 3 days ago
Quality Improvement Specialist managing HEDIS projects, data reporting, audits, and process improvements. Supporting Centene’s healthcare quality initiatives for members and providers.
🕒 3 days ago
Health care quality specialist improving Medicaid and CHIP outcomes for CVS Health. Supporting NCQA accreditation, performance improvement projects, data analysis, and quality committees.
🇺🇸 United States – Remote
💵 $43.9k - $85.1k / year
💰 Pre Seed Round on 2022-03
⏰ Full Time
🟡 Mid-level
🟠 Senior
🕒 6 days ago
Validation Specialist leading ETQ Reliance and QMS validation for CGI’s life sciences consulting clients. Ensuring FDA, GxP, and 21 CFR Part 11 compliance.