• Partner directly with client stakeholders to understand technical requirements and align them to business objectives • Plan and lead implementation engagements — deploying solution components and configuring the product to meet each client's specific environment • Collaborate across internal teams and client organizations to ensure smooth rollout and successful integration of BigID solutions • Deliver technical training tailored to the audience, from hands-on admins to executive stakeholders • Identify root causes of deployment issues and drive them to resolution • Work closely with Engineering and Product Management to document field issues, enhancement requests, and opportunities to improve the implementation process

• Functional administration and maintenance of our 12c Oracle Identity Management application including Oracle Access Manager (OAM), Oracle Internet Directory (OID), and Oracle Identity Governance (OIG) • Provide support to and participate in IAM continuous monitoring activities including monitoring new and removed identities, access and permissions changes, privilege escalation, bot activity, and other related activities • Support user access provisioning, authentication, and access management processes • Actively participate in troubleshooting sessions for OIG/OAM in Prod and Non-Prod • Develop and maintain system documentation, including standard operating procedures (SOPs) and configuration guides • Coordinate and collaborate with technical subject matter experts (SMEs) to ensure technical and operational security controls are operating as expected

Role Description TerraPower is seeking a highly motivated Nuclear Licensing Engineer to be a part of the Natrium® Licensing team. This position reports to a Licensing Director and provides licensing support to Natrium advanced reactor projects, develops licensing documents, and supports regulatory audits and engagements. Work will be in close consultation with Engineering staff and will ensure Licensing documents are created in accordance with TerraPower licensing strategy and guidance. Support for engagements with the US Nuclear Regulatory Commission (NRC) includes: - Pre-application meetings - Preparing and reviewing permit and license applications - Preparing and reviewing topical reports - Responding to NRC audit questions and requests for additional information Qualifications - Bachelor’s degree in engineering from an accredited, four-year university or equivalent experience - Capability and willingness to adhere to strict quality assurance standards - Demonstrated, applicable experience in nuclear licensing, or comparable field - Ability to analyze and interpret U.S. NRC regulations and guidance - Experience with U.S. NRC construction permit and operating license application preparation and/or reviews - Project management experience, including developing and maintaining schedules; meeting deadlines; formulating budgets; and leading teams - Understanding of nuclear reactor design and operation - Self-Starter with ability to manage deadlines - Proficient in MS Office Suite (Word, PowerPoint, Outlook, Excel) and Adobe Professional - Strong communication skills - The successful candidate will possess a high degree of trust and integrity, communicate openly and display respect and a desire to foster teamwork Requirements - Motor Abilities: Sitting for extended periods, bending/stooping, grasping/gripping, fine motor control (hands) - Physical exertion and/or requirements: Minimal, with ability to safely lift up to 25 pounds - Repetitive work: Prolonged - Special Senses: Visual and audio focused work - Work Conditions: Stairs, typing/keyboard, standard and/or sitting working environment of >8 hours/day - Travel required: 0-10% Benefits - Competitive Compensation - Salary, eligible to participate in discretionary short-term incentive payments - Comprehensive Medical and Wellness Benefits - Medical - Vision - Dental - Life and Disability - Gender Affirmation Benefits - Parental Leave - 401k Plan - Generous Paid Time Off (PTO): 21 days of annually accrued PTO - Generous Holiday Schedule: 10 paid holidays - Relocation Assistance - Professional and Educational Support Opportunities

Role Description Syner-G is seeking a highly experienced Staff Process Engineer / MSAT Technology Transfer Lead with 10–15+ years of biologics manufacturing experience to provide technical and program leadership for a portfolio of monoclonal antibody (mAb) drug substance technology transfers. This role will be responsible for managing approximately 10 concurrent technology transfer programs, driving cross-functional execution from process transfer through GMP manufacturing and PPQ, while ensuring technical readiness, risk mitigation, and milestone achievement. The successful candidate will serve as a strategic partner to MSAT leadership, establishing governance, portfolio reporting, resource planning, and escalation processes that improve execution visibility and accountability. Leveraging deep expertise in mammalian cell culture, downstream purification, process validation, and commercial manufacturing, the Staff Process Engineer will support transfer strategies, validation planning, process risk assessments, and commercialization activities. The ideal candidate will combine strong program leadership capabilities with hands-on process development and manufacturing science experience to support technical troubleshooting and execution as needed. Qualifications - BS or MS in Chemical Engineering, Biochemical Engineering, Bioprocess Engineering, Biotechnology, or a related technical discipline preferred. - 10–15+ years of experience in MSAT, process engineering, process development, technology transfer, or biologics manufacturing within biotechnology or pharmaceutical organizations. - Demonstrated experience managing multiple concurrent technology transfer programs for biologic products, preferably monoclonal antibodies. - Extensive expertise in upstream and downstream biologics manufacturing processes, including mammalian cell culture, chromatography, viral clearance operations, filtration, and UF/DF. - Hands-on experience supporting process development, manufacturing investigations, scale-up, process characterization, and technology transfer activities. - Strong knowledge of GMP manufacturing, process validation, PPQ execution, lifecycle validation, and regulatory expectations for commercial biologics manufacturing. - Proven leadership of cross-functional technical teams and complex manufacturing or commercialization programs. - Experience developing portfolio governance, resource planning, risk management, and program reporting frameworks is highly desirable. - Prior MSAT leadership or technical program management experience supporting commercial biologics products preferred. Requirements - Deep understanding of mAb drug substance manufacturing processes and technology transfer methodologies. - Strong knowledge of process validation, PPQ strategy development, process characterization, CPP/CQA assessment, and risk management principles. - Experience with manufacturing scale-up, process monitoring, statistical analysis, and process performance evaluation. - Ability to assess technical readiness, identify process risks, and develop mitigation strategies across multiple programs. - Strong project and portfolio management capabilities, including management of schedules, resources, budgets, and competing priorities. - Excellent communication, stakeholder management, leadership, and influencing skills. - Ability to operate effectively in fast-paced, highly matrixed environments supporting multiple simultaneous programs. Benefits - Market competitive base salary and annual incentive plan. - Robust benefit offerings. - Ongoing recognition and career development opportunities. - Generous flexible paid time off program. - Company-paid holidays. - Flexible working hours and fully remote work options for most positions. - Office locations in Greater Boston; San Diego, CA; Boulder, CO; and India for those who prefer a physical work location. Company Description A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact.