RN QUALITY SPECIALIST Role Summary Provides remote, patient-centered case management support and education to assigned patients. The role focuses on relationship building, care coordination, and navigation of insurance and pharmacy protocols to support medication access, adherence, and disease-state education. Essential Functions - Adhere to all program-specific contractual agreements, company policies, quality standards, and compliance requirements. - Build and maintain therapeutic relationships with assigned patients throughout the duration of the program. - Deliver patient-centric education regarding treatments, disease states, and prescribed products. - Manage a designated caseload including scheduled outreach, adherence monitoring, and accurate documentation in program databases. - Coordinate interactions between patients and internal or external clinical partners as appropriate. - Customize interactions based on individual patient needs, health literacy, and program requirements. - Participate in program-specific customer meetings, training sessions, and orientations. - Demonstrate clinical competency and system proficiency as validated through required assessments. - Support special projects and additional duties aligned to contract performance and business needs. Schedule - Hours: 11:00 a.m. – 8:00 p.m. Eastern Time Required Qualifications - Active, unrestricted Registered Nurse (RN) license in primary state of residence; compact license required. - Minimum of two (2) years of RN clinical experience. - Demonstrated proficiency with Microsoft Office applications and basic database navigation. - Strong verbal and written communication skills. - Ability to manage multiple priorities, meet deadlines, and work independently in a remote environment. Preferred Qualifications - Bachelor of Science in Nursing (BSN) or active enrollment in a BSN program. - Case management or care coordination experience. - Knowledge of pharmacy operations, pharmaceuticals, life sciences, or healthcare business environments. Core Competencies - Patient-focused and quality-driven approach to care. - Collaboration and teamwork across multidisciplinary partners. - Accountability, ownership, and results orientation. - Professional judgment and adherence to ethical standards. If you will be working at home occasionally or permanently, the internet connection must be obtained through a cable broadband or fiber optic internet service provider with speeds of at least 10Mbps download/5Mbps upload. For this position, we anticipate offering an hourly rate of 33 - 56 USD / hourly, depending on relevant factors, including experience and geographic location. This role is also anticipated to be eligible to participate in an annual bonus plan. At The Cigna Group, you’ll enjoy a comprehensive range of benefits, with a focus on supporting your whole health. Starting on day one of your employment, you’ll be offered several health-related benefits including medical, vision, dental, and well-being and behavioral health programs. We also offer 401(k), company paid life insurance, tuition reimbursement, a minimum of 18 days of paid time off per year and paid holidays. For more details on our employee benefits programs, click here. About Evernorth Health Services Evernorth Health Services, a division of The Cigna Group, creates pharmacy, care and benefit solutions to improve health and increase vitality. We relentlessly innovate to make the prediction, prevention and treatment of illness and disease more accessible to millions of people. Join us in driving growth and improving lives. Qualified applicants will be considered without regard to race, color, age, disability, sex, childbirth (including pregnancy) or related medical conditions including but not limited to lactation, sexual orientation, gender identity or expression, veteran or military status, religion, national origin, ancestry, marital or familial status, genetic information, status with regard to public assistance, citizenship status or any other characteristic protected by applicable equal employment opportunity laws. If you require reasonable accommodation in completing the online application process, please email: SeeYourself@cigna.com for support. Do not email SeeYourself@cigna.com for an update on your application or to provide your resume as you will not receive a response. The Cigna Group has a tobacco-free policy and reserves the right not to hire tobacco/nicotine users in states where that is legally permissible. Candidates in such states who use tobacco/nicotine will not be considered for employment unless they enter a qualifying smoking cessation program prior to the start of their employment. These states include: Alabama, Alaska, Arizona, Arkansas, Delaware, Florida, Georgia, Hawaii, Idaho, Iowa, Kansas, Maryland, Massachusetts, Michigan, Nebraska, Ohio, Pennsylvania, Texas, Utah, Vermont, and Washington State. Qualified applicants with criminal histories will be considered for employment in a manner consistent with all federal, state and local ordinances.

Syndax Pharmaceuticals is looking for a Contractor, Senior GMP Quality Assurance At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. The Role: Reporting to the Senior Director, Commercial Quality, Contractor, Senior GMP Quality Assurance will be responsible for lot review/release activities for drug substances, drug products, and finished goods by Contract Manufacturing Organizations (CMOs). Throughout the process, ensure Syndax, its affiliates and/or contractors associated with the manufacture, packaging, labeling, testing, storage and distribution of products used for commercial distribution comply with cGMPs and standards established by company as well as regulations of applicable authorities. Key Responsibilities: - Support commercial batch review and release activities for drug substance, drug product, and /or finished goods for all phases of development including review and approval of Master Batch Records along with executed batch records. - Leads and maintains effective relationships with Contract manufacturing and testing Organizations. - Provide support for Process Validation and Technical transfer activities with existing and new vendors. as needed. - Provide support to cross functional teams in GMP compliance interpretation, consultation, training, and recommendations. - Collaborates cross-functionally other functions, such as CMC, Regulatory, Development QA, as needed to ensure alignment and best practices. - Effectively interact with external contract manufacturers and testing laboratories as well as work as part of an internal multidisciplinary team to support manufacturing and testing of materials supporting Syndax development programs - Manage and address associated investigations, CAPAs, change controls, OOS, etc. - Support investigations into quality issues with focus on product impact and patient safety; facilitate identification of root cause and development of appropriate corrective and preventive actions; track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities, as appropriate. - Identify and mitigate GMP activities and process improvement initiatives as requested by management. - Work closely with the Quality Assurance team to ensure alignment and compliance with Syndax Quality Systems. - Support Commercial Quality activities like APQR, Mock Recall, etc. - Self-motivating and independent. - Work independently with guidance from managers and senior staff. - Must be able to articulate complex issues clearly verbally and written. - Author, review, and/or approval of documents including deviations, SOPs, and protocols. Desired Experience/Education and Personal Attributes: - BS degree in scientific field required, advanced degree preferred. - Minimum of 10 years of experience in the pharmaceutical industry, within the QA/GMP environment. - Small molecule experience required (drug substance/API, drug product, packaging and labeling) and QC/analytical. - Must have experience working in cross-functional teams including CMC, analytical, supply chain, and regulatory affairs, medical affairs, and commercial. - Experience working with external vendors and suppliers including drug substance/API, drug product, analytical, and/or secondary packaging and labeling. - Experience using QMS (including electronic systems), including documents and SOPs, change controls, deviations, product complaints, and annual product reviews. Familiarity with Veeva is a strong plus. - Extensive understanding and application of 21 CFR 210/211 and Part 11, ICH GMP, and other applicable global regulations. - Experience preparing for and participating in GMP regulatory inspections. - Strong technical writing skills; ability to write clear quality position statements, and procedures. - Excellent communication skills. - Self-motivating, proactive and independent. Location: Remote About Syndax: Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include a menin inhibitor for R/R acute leukemia and a monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com/ or follow the Company on X and LinkedIn. Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law. #LI-REMOTE

• Perform Active Directory penetration testing to identify privilege escalation paths, insecure configurations, and potential lateral movement opportunities. • Conduct internal and external network penetration tests to identify vulnerabilities and weaknesses within the enterprise infrastructure. • Perform web application penetration testing, including authentication testing, input validation, session management, and business logic testing. • Identify and analyze security misconfigurations across systems, services, and network infrastructure. • Conduct security audits and configuration reviews to identify gaps against security best practices and industry standards. • Perform risk assessments by evaluating vulnerabilities, misconfigurations, and their potential business impact. • Document security findings, misconfigurations, and vulnerabilities with clear risk ratings and remediation guidance. • Participate in purple team engagements by simulating attacker techniques and helping SOC teams improve detection and response capabilities. • Support threat simulation exercises based on real-world attack techniques and frameworks such as MITRE ATT&CK. • Work closely with SOC and defensive teams to improve alerting, monitoring, and threat detection use cases. • Assist in validating remediation efforts by performing retesting and verification of fixes. • Prepare technical and executive-level reports summarizing findings, risks, and recommended mitigation strategies.

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description We’re looking for a Lead QA Engineer to join our team 🚀 - Support and improve QA, TLC, and SDLC processes, taking responsibility for the growth and productivity of QA team members - Continuously develop and expand the QA team’s expertise and capabilities - Organize and maintain test documentation - Be responsible for communication with the product and developer team - Collaborate with other teams and departments to ensure the product meets business expectations Qualifications - 3+ years of testing experience in a Lead QA position and 4+ years of QA experience before the Lead position - Deep knowledge of testing theory, understanding of web technologies - Ability to focus on multiple tasks simultaneously - Strong problem-solving, people management, and negotiation skills - Proactive mindset - Attentive to the details - Understanding of web technologies (HTTP, HTML, CSS, JavaScript, JSON) - Ability to work with databases (SQL) - Rich experience working with log analysis tools (e.g., Kibana, Grafana) - Rich experience testing REST APIs (e.g., Swagger, Postman) - Advanced user of Chrome DevTools and equivalent browser tools to reproduce complex issues, collect and analyze diagnostic artifacts (console, network, HAR), and perform accurate root cause analysis - Strong knowledge of software quality assurance methodologies Requirements - Automation experience (we are using Playwright\TypeScript) - Experience in the iGaming/Betting domain - Jira advanced user - AI(LLM) enthusiast - GLI certification experience Benefits - Work-life balance — even in challenging times - Choose where and how to work — from home, the office, or anywhere in the world - Flexible schedule — we value your life rhythm - Gifts, giveaways, training, team buildings, and corporate events — you’ll never be bored with us! - Internal training, mentoring, access to courses - Career growth without bureaucracy - Annual paid leave: 20 working days + 5 additional days off - Paid sick leave: 15 days per year - Professional support: access to psychologist consultations (compensation package may be extended) - Online development: regular webinars, workshops, and trainings on both professional and general topics Company Description Turbo Stars is a multi-product IT company delivering fast, high-quality, and cutting-edge B2B solutions for the iGaming industry.