About Us DLH delivers improved health and national security readiness solutions for federal programs through science research and development, systems engineering and integration, and digital transformation. Our experts in public health, performance evaluation, and health operations solve the complex problems faced by civilian and military customers alike by leveraging advanced tools – including digital transformation, artificial intelligence, data analytics, cloud enablement, modeling, and simulation, and more. With over 2,400 employees dedicated to the idea that “Your Mission is Our Passion,” DLH brings a unique combination of government sector experience, proven methodology, and unwavering commitment to innovation to improve the lives of millions. Overview The Director, Quality Management Organization (QMO), provides visionary strategic, operational, and technical leadership to ensure the highest standards of quality and regulatory compliance across a diverse research enterprise. This critical role commands a broad span of control, overseeing quality and regulatory systems for an active public health and scientific research organization encompassing complex, multi-site clinical trials, clinical, observational, and epidemiological research. The Director manages all aspects of quality management, process optimization, regulatory alignment, professional writing, proposal development, business development activities, and continuous improvement to support organizational goals, compliance obligations, and research excellence. Responsibilities - Provide enterprise-wide leadership and oversight for multi-disciplinary quality and regulatory teams supporting clinical trials, epidemiological research, BSL-2 laboratory biospecimen processing, and survey-based projects. - Direct the development, implementation, and continual improvement of the Quality Management Plan (QMP) and related Standard Operating Procedures (SOPs), ensuring integration of risk-based quality management practices and robust internal controls across all research activities. - Ensure strict compliance and alignment with all applicable federal (FDA, NIH, CDC), international (ICH GCP, GLP, ISO), regulatory, contractual, biosafety (including BSL-2), human subject protection (HHS/OHRP, IRB), and privacy (HIPAA) requirements. - Oversee the implementation and enforcement of biosafety management systems and maintain the integrity and inspection readiness of all regulatory and quality documentation, including electronic systems and Trial Master Files. - Develop and execute comprehensive audit and inspection programs, manage CAPA processes, and directly engage with sponsors, regulatory agencies, and external assessors, leading remediation and continuous improvement efforts. - Recruit, mentor, and professionally develop quality assurance, quality improvement, and regulatory staff to sustain high-performing, cross-functional teams suited for high-complexity research environments. - Serve as the organization’s principal subject matter expert and liaison on quality and regulatory affairs, engaging with regulatory bodies, sponsors, clients, IRBs, accrediting agencies, and internal leadership. - Lead and contribute to professional writing, technical proposal development, statements of work, and responses to RFPs/RFIs, supporting business development activities and showcasing organizational quality and regulatory capabilities. Qualifications - Bachelor's or Master’s degree in biomedical science, public health, laboratory science, clinical research, quality/regulatory discipline, or a related field. - At least 12 years of experience with a Master's degree OR 14 years of experience with a Bachelor's degree of progressive quality and regulatory management experience in clinical, biomedical, or laboratory research organizations, including 6 years in a leadership or director-level role. - Demonstrated expertise in quality assurance and regulatory oversight of multi-site clinical trials, with advanced knowledge of federal, international, and sponsor regulations (e.g., FDA, 21 CFR, ICH GCP, GLP, BSL-2, CLIA, ISO, OHRP, HIPAA, IRB/ethics). - Proven record of successful audit/inspection readiness and compliance, including substantial experience planning for, managing, and hosting sponsor, client, and regulatory audits, as well as developing and managing QMPs and SOPs in complex research environments. - Strong professional, scientific, and technical writing skills, including the development of quality and regulatory content for proposals, RFPs, and business development. - Exceptional leadership, analytical, and cross-functional collaboration skills; proficiency with electronic quality, document, and biospecimen/data management systems; and outstanding communication with regulatory authorities, sponsors, and multidisciplinary research teams. - Preferred - Doctoral degree (PhD, PharmD, MD) in a relevant scientific, biomedical, or regulatory field. - Preferred - Certification such as RAC (Regulatory Affairs Certification), ASQ CQE/CQA, or equivalent. - Preferred - Experience with accreditation processes (e.g., CAP, CLIA) and international research standards. - Preferred - Demonstrated knowledge of FDA regulatory process and landscape, including familiarity with key regulatory pathways (e.g., IND, NDA, BLA, 510(k), PMA) and documentation requirements - Preferred - Experience interpreting and applying current FDA regulations, guidance documents, and best practices throughout the product development lifecycle is highly desirable Basic Compensation: $140,000 - $160,000 yearly salary The salary range listed reflects what we reasonably expect to pay for this role at the time of posting. The final offer may vary based on skills, experience, geographic location, market conditions, and internal equity. Additional compensation may include performance incentives and program-specific awards. We do not use salary history to determine compensation, in line with applicable law. Benefits DLH Corp offers our employees an excellent benefits package, including Personal Time Off (PTO), medical, dental, vision, supplemental life with AD&D, short and long-term disability, flexible spending accounts, parental leave, legal services, and more. We want our employees to save for their future; therefore, we offer a 401(k) Retirement Plan, which includes a matching component. DLH is dedicated to your career development, providing training to help drive success, with access to our best-in-class e-learning suite for formal and informal learning, professional and technical certification preparation, and education assistance at accredited institutions. #LI-REMOTE EEO DLH Corporation is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment. DLH will provide reasonable accommodation to individuals with disabilities and disabled Veterans who need assistance to apply.

Selene Holdings is a multiple-lines business financial services firm with a mortgage servicing company, a loan diligence company, a title company, an insurance brokerage, and a real estate owned company. We have office locations in Dallas, TX, Jacksonville, FL, and Salt Lake City, UT. Founded in 2007 to address needs in the mortgage industry, Selene strives to provide amazing client and borrower experiences. A positive attitude coupled with proven creative thinking and actions are all attributes we seek in every one of our employees. If you want to make a difference, then Selene is the place for you! Position Overview We are seeking a detail oriented and technically skilled QA Test Builder and Technical Analyst to join our Mortgage Servicing team, with a primary focus on process design and test development within the ACES Quality Management System. The ideal candidate will play a key role in designing, building, and executing comprehensive quality assurance test cases while delivering technical analysis to support mortgage servicing operations. This position requires a strong blend of quality assurance expertise, mortgage servicing experience, and advanced technical proficiency with the ACES platform. Key Responsibilities - Serve as the Quality Assurance department’s primary ACES Quality Management System SME, leading test design, configuration guidance, data mapping and integrity validation, reporting structure, and best practice QA methodologies to ensure optimal platform performance, compliance, and operational excellence. - Collaborate with business stakeholders, IT teams, and ACES administrators to gather requirements, clarify test objectives, troubleshoot issues, and support end-to-end testing initiatives. - Analyze business requirements and translate them into effective test plans and solutions to ensure ACES system integrity and regulatory compliance. - Develop, document, and execute comprehensive QA test cases, scripts, and checklists within the ACES platform for mortgage servicing processes. - Identify, document, and track defects, process gaps, and system inconsistencies within ACES and across mortgage servicing workflows. - Perform root cause analysis on defects and recommend solutions that enhance process efficiency and system performance. - Prepare detailed reporting on test execution, defect trends, and system performance for leadership review. - Ensure compliance with investor, regulatory, and servicing requirements in all test scenarios, documentation, and validation activities. - Coordinate and support User Acceptance Testing (UAT) with business partners and endusers, ensuring readiness and accuracy. - Maintain and continuously update QA documentation, technical workflows, and test assets as system changes occur. - Map, validate, and reconcile data between mortgage servicing systems and the ACES platform to ensure accuracy, consistency, and audit readiness. - Design and maintain data mapping documentation, integration workflows, and migration procedures to support system alignment and operational accuracy. - Develop, generate, and distribute periodic and adhoc QA reports using ACES and other reporting tools, delivering insights on quality trends, testing results, and performance metrics. - Partner with stakeholders to define reporting needs and deliver actionable analytics that support compliance, operations, and continuous improvement. - Support system upgrades, configuration changes, and new module implementations by providing QA expertise and technical analysis. Qualifications - Bachelor’s degree in Computer Science, Information Technology, Business Administration, or a related field (or equivalent experience). - 5+ years of experience in quality assurance/quality control/compliance/risk testing, technical analysis, or business analysis within the mortgage servicing or financial services industry. - Hands-on experience with the ACES Quality Management System or similar QA platforms is highly preferred. - Strong understanding of mortgage servicing operations, including compliance and regulatory requirements. - Proficiency with SQL, including writing queries, working with relational databases, and interpreting data sets. - Excellent analytical, problem solving, and troubleshooting skills, with the ability to evaluate issues and recommend effective solutions. - Strong written and verbal communication skills, capable of translating complex technical concepts for nontechnical audiences. - Ability to work both independently and collaboratively in a fast paced, deadline driven environment. - High attention to detail with a commitment to delivering accurate, high quality work. - Experience with data mapping, systems integration, and data migration between mortgage servicing systems and QA platforms. - Background in designing and generating QA and operational reports, including proficiency with ACES reporting tools or similar systems. Preferred Skills - Previous experience with ACES system configuration, workflow design, or automation tools. - Knowledge of mortgage loan servicing systems and investor guidelines (Fannie Mae, Freddie Mac, FHA, VA, etc.). - Strong knowledge of data mapping techniques and common reporting frameworks in mortgage servicing. Why Selene? Benefits Selene Finance LP is committed to the total wellbeing of its employees and therefore offers one of the best benefits packages available in the industry today, which includes: - Paid Time Off (PTO) - Medical, Dental &Vision - Employee Assistance Program - Flexible Spending Account - Health Savings Account - Paid Holidays - Company paid Life Insurance - Matching 401(k) Plan The job requirements listed above are representative of the knowledge, skills, and/or abilities required. This job description is not an inclusive list of all duties and responsibilities of this position. Incumbents will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. Selene reserves the right to amend and change responsibilities to meet business and organizational needs. Privacy Policy - Selene (seleneadvantage.com)

• Analyze, design, implement, troubleshoot, and maintain commercial, and cloud-native security solutions across public cloud environments • Create and maintain automated workflows and integrations to support cloud security controls and the automation platform, primarily using Python • Identify and define security system requirements for public cloud environments • Continuously analyze security systems and drive improvements, with a focus on automation and resilience • Develop, document, and maintain configuration and security standards, technical documentation, and standard operating procedures (SOPs) • Tune, filter, and customize security systems with Information Security Analysts to reduce noise and improve detection quality • Serve as a subject matter expert for public cloud security and security automation • Consult with team members and other groups to solve basic to moderately complex cloud-focused security challenges • Partner with teams outside of Security (e.g., application, infrastructure, DevOps/Platform) to design secure, automated cloud architectures and guardrail • Lead and contribute to medium to large security and automation projects • Build project plans based on requirements analysis and stakeholder input • Communicate project status, risks, and metrics to leadership • Support audit, compliance, and regulatory activities, including but not limited to PCI DSS, SOX, and evolving privacy laws • Provide evidence, explanations, and remediation input for controls related to public cloud security and associated automation • Participate in incident response activities by reviewing and analyzing security events and incidents • Use automation (e.g., Python-based tooling and workflows) to enhance speed and consistency of response

Who we are! Elementl Power Inc. is an advanced nuclear project developer and independent power producer, building scalable pathways for clean resilient energy. We break the stalemate in advanced nuclear deployment by delivering turnkey development, financing, and ownership solutions -- empowering customers to access nuclear power without the burden of operating assets. The Opportunity We’re excited to add a Quality Assurance Manager to our growing team at Elementl. Reporting to the SVP, Licensing & Regulatory Affairs, this role leads the development and execution of our Nuclear Quality Assurance (NQA) program across a portfolio of nuclear power plant (NPP) projects. You’ll serve as Elementl’s Quality Assurance subject matter expert, shaping how quality is implemented in practice across engineering, procurement, fabrication, and construction. This role sits at the center of project execution; working closely with the Chief Development Officer, project leadership, and functional teams to ensure quality is embedded from early site work through commissioning. We’re looking for a seasoned nuclear quality professional who understands what it takes to operationalize a compliant, effective QA program in a complex, multi-party environment. You bring deep familiarity with 10 CFR Part 50 Appendix B and NQA-1, and you know how to translate requirements into practical systems, oversight, and behaviors that hold up under regulatory scrutiny.