• Provide regulatory subject matter expertise and act as an internal consultant on assigned work. • Manage large multi-disciplinary regulatory projects. • Analyze workflows and understand policies, procedures, and constraints of the clinical or business operations related to regulatory requirements. • Conduct in-depth investigations and documentation of operational & report specifications. • Analyze new application releases to determine regulatory build and reporting needs. • Act as a mentor to new and less experienced application analysts. • Track, read and analyze new rulemaking and annual updates to existing regulations. • Maintain Epic certifications.

XO Health believes healthcare is fixable. Become part of the community changing the face of the industry. XO Health is the first health plan designed by and for self-insured employers that delivers a more unified health experience for everyone – from those who receive care, to those who deliver it, to those who pay for it. We are growing a multi-disciplinary team of diverse and digitally empowered employees ready to rebuild trust in healthcare through comprehensive and unified transformation. Risk Solutions Actuarial Associate About the Role XO Health is redefining how risk is structured, priced, and managed across self-funded employer health plans and provider partnerships. We’re looking for a quantitatively minded, self-starting early-career actuary to join our Risk Solutions team. This individual will help build and scale the risk backbone of our products, with direct visibility into executive strategy, product development, and risk operations. In this role, you’ll work across teams to develop pricing models, monitor financial performance, evaluate partner and provider risk, and support strategies that bring clarity, transparency, and predictability to health plan costs. This role will have a front-row seat for our innovative alternative payment model platform, and its impact across our stakeholders What You'll Do Support and develop the actuarial modeling behind XO’s risk-sharing and value-aligned models , including provider performance pricing and evaluation, employer pricing, and financial insight into risk-based contracts. Manage XO Health’s stop-loss and reinsurance strategy , including product design for small and mid-market employers, provider risk strategies, pricing input, partner management, and performance tracking, across both employers and Providers. Support RFPs and maintain relationships with MGUs, captives, and carriers to help external partners evaluate and price XO’s unique model. Advance XO’s differentiated high-cost claim strategy, leveraging our unique position across both employers and providers to manage risk more proactively and equitably. This includes developing analytics and interventions that span clinical, financial, and contractual levers. Support reporting and communications on financial performance, risk solutions, pricing strategy, and model assumptions for both internal and external stakeholders, including executive team and advisory and corporate boards Own end-to-end execution of cross-functional initiatives, working with teams across analytics, finance, commercial, clinical, and provider strategy to build scalable, tech-enabled pricing and risk capabilities. What You Bring

Do you thrive where technology, compliance, and product development converge? Do you see regulatory expertise as a way to fuel innovation, not slow it down? Do you enjoy collaborating with product managers and engineers to design solutions that are both secure and user-friendly? AOT Technologies is looking for a Compliance Analyst . Join our team to help integrate regulatory requirements into our products and processes as we scale across North America and Europe. About AOT We're on a mission to help enterprises and governments bring their ideas to life. As a boutique consulting firm, we partner with enterprises, startups, and governments to solve complex, mission-critical challenges. Our expertise spans business process management, automation and AI, cloud, and application development. Our teams are collaborative, our leadership is transparent, and our work is impactful. Alongside our consulting practice, we’re product builders: our flagship platform, formsflow.ai , is a low-code solution that simplifies complex form creation, approvals, and workflow automation, helping organizations move faster without sacrificing quality or compliance. Under the SLED360 umbrella, we deliver products and services tailored to the unique needs of state and local governments and the education sector, from modern case management to digital services. Our product offerings reflect our entrepreneurial spirit and firsthand experience solving real-world problems with scalable, human-centered technology. As we expand into new markets and scale our solutions, there’s never been a better time to join AOT. Role & Responsibilities As Compliance Analyst, you’ll ensure that compliance is not just an afterthought, but a core part of how we design, build, and scale. You’ll bring structure, foresight, and creativity to embed compliance into our SaaS solutions. Your work will directly impact client trust and regulatory readiness in a fast-moving SaaS environment. You will: Partner with product managers and engineers to ensure compliance is built in to products, workflows, and infrastructure Translate complex regulatory requirements into product-friendly guidance Monitor compliance with Canadian, U.S., and European standards, including HIPAA, SOC2, ISO, and GDPR Lead and support audit processes, coordinating with internal stakeholders and external auditors Proactively influence organizational compliance Conduct risk assessments and draft reports with prioritized remediation plans Analyze and align AOT’s systems with data protection protocols (encryption, messaging, storage) Please note that this role is regularly required to collaborate across multiple time zones – e.g., IST, CET (about 8 hours per week). Who You Are You bring curiosity, structure, and a calm under pressure that helps others feel confident in complex regulatory landscapes. You’re experienced enough to own audits, and versatile enough to learn new frameworks on the fly. You have the mindset of a builder and see compliance as a product feature and a competitive advantage. Bachelor’s degree in business administration, software engineering, or related disciplines 3–5 years in compliance, risk management, or audit in SaaS or highly regulated industries Familiarity with HIPAA, SOC2, ISO standards, and GDPR/Canadian privacy regulations Skilled with tools like Excel, Power BI, Jira, and compliance tracking platforms Knowledge of HL7, FHIR, and encryption protocols for data at rest and in transit Comfortable operating across North American and global regulatory environment Nice to Have Understanding of SaaS, software development, and product management practices Direct experience in software development or product management Must be located in and legally authorized to work in the United States. What We Offer $60K–$80K USD base salary Remote-first work environment Flexible schedules and generous paid time off Competitive health, dental, and wellness benefits from Day 1 Employer-sponsored deferred profit-sharing plan Career development support, including mentoring, training, and professional development budget A collaborative, mission-driven culture where your work matters Living AOT's Values Our values guide how we work, collaborate, and grow as a team. Every role at AOT is expected to embody and promote these values: Innovation: We pursue true innovation by solving problems and meeting unarticulated needs. Integrity: We hold ourselves to high ethical standards and never compromise. Ownership: We are all responsible for our shared long-term success. Agility: We stay ready to adapt to change and deliver results. Collaboration: We believe collaboration and knowledge-sharing fuel innovation and success. Empowerment: We support our people so they can bring the best of themselves to work every day. Apply Now Apply today – we’re hiring now and excited to meet you. We strongly encourage candidates of all backgrounds, experiences, and identities to apply, even if they don't meet 100% of the listed criteria. We are seeking candidates with diverse career experiences for this position. If you're passionate about impacting the tech industry and eager to contribute your expertise, we invite you to apply! Closing Date: February 24, 2026 at 12:00 AM PST

Company Overview: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases. Position Overview: Beam is seeking a highly skilled Specialist I/II to join our growing Digital Quality & Data Integrity team and play a pivotal role in shaping the future of digital compliance. Unlike traditional QA roles, this position focuses on advanced computerized systems quality assurance and data integrity across local embedded computerized systems and global platforms—including SaaS, IaaS, and PaaS—critical to our digital transformation. As a trusted Subject Matter Expert, you will partner with Manufacturing, Quality Control, Validation (CQV and CSV), IT, and Automation teams to ensure seamless qualification, validation, and automation activities that meet GxP and regulatory standards. This is your opportunity to influence enterprise-wide digital strategies, drive innovation, and make a measurable impact on patient safety and product quality. Responsibilities: Oversee risk-based Computerized System Validation (CSV)/Computerized Software Assurance (CSA) activities across Manufacturing, QC, IT, Automation and Global Platforms, ensuring 21 CFR Part 11/Annex 11 and Beam’s internal policies and procedures. Support review and approval of validation lifecycle documents including but not limited to SIA, URS/SRS, CS, FDS, IQ, OQ, PQ, RTM and VSR, for embedded computerized systems and global platforms. Support authoring of CSV lifecycle and test documents, risk assessments and gap assessments as required. Collaborate with IT system owners, business systems owners, validation and product quality to deploy robust data integrity controls across systems and processes. Participate in Change Management activities to ensure controlled evaluation, qualification, and deployment of changes. Serve as SME and/or Quality approver on QMS records including change controls, continuous improvements, CAPAs, deviations and supplier qualification associated with computerized systems and data integrity. Review and ensure validation compliance for infrastructure systems such as DeltaV, MES, OSI PI, BAS, Clinical and Cloud systems. Act as data integrity SME by ensuring the enforcement of ALCOA+ principles and identifying critical data risks across manufacturing processes, QC methods, and computerized systems. Actively participate in the development of data integrity gap assessment program and assessment tools and eventual gap remediation activities by supporting identification of short term and long term mitigation strategies. Contribute to improvements in CSV/CSA and data integrity policies and procedures, user/functional group SME training and guidance. Support periodic review activities - periodic reviews of computerized systems, user access reviews, audit trail reviews, periodic validation reviews and periodic procedure reviews and updates to maintain compliance. Qualifications: Bachelor’s degree in Engineering, Computer Science, Life Sciences, or a related field with 10+ years of relevant experience; or Master’s degree in the same fields with 8+ years of relevant experience. Experience working in Quality Assurance, Validation, or IT Quality Assurance roles within the biotechnology or pharmaceutical industry. Experience working with systems like DeltaV, OSI PI, BAS, Kneat, Veeva, MES or comparable automation and data systems. Familiarity working with manufacturing platforms such as Rotea, Sepax, LOVO, Cue, Prodigy, MaxCyte, Skid Controllers and platform integrations with DeltaV is preferred. Experience with analytical instruments such as Spectramax, Zetasizer, MACSQuant, SoloVPE, BacT with MYLA software, and other laboratory instruments. Experience with supplier management program for computerized system suppliers. Strong operational knowledge of risk-based tools, ALCOA+ principles, FDA and MHRA data integrity guidance, and 21 CFR Part 11/Annex 11 regulations is preferred. Prior experience working as a QA reviewer for embedded computerized systems – manufacturing equipment(s) and analytical instruments. Proven ability to implement cross-functional remediation plans aligned with the regulatory expectations for CSV/CSA and data governance. Excellent written and verbal communication skills; ability to collaborate across functions. Ability to work independently, manage prioritize competing priorities, and maintain compliance under tight timelines. Ability to lead and implement changes in QA capacity in a fast-paced and diverse environment. This position will require to be on-site at Beam’s RTP location. The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data. Beam Pay Range $105,000 — $145,000 USD