Role Description We are looking for a detail-oriented and adaptable Senior Analyst to join our team. The ideal candidate thrives in a dynamic environment, embraces change, and takes ownership of their work. This role requires strong analytical and problem-solving skills, as well as the ability to interpret complex data and present insights to senior leadership. The Sr. Analyst of Commercial Excellence will report to the Manager of Commercial Excellence. They will be responsible for: - Analyzing and presenting data - Optimizing processes - Supporting executive reporting They should be comfortable working independently while also contributing to a team environment, sharing insights, and collaborating with peers and cross-functional teams to support business objectives. Strong organizational skills, a proactive mindset, and an ownership mentality will be key to success. Qualifications - Strong analytical and problem-solving skills - Ability to interpret complex data - Experience in presenting insights to senior leadership - Detail-oriented and adaptable Requirements - Comfortable working independently - Ability to collaborate with peers and cross-functional teams - Strong organizational skills - Proactive mindset - Ownership mentality Benefits - Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours - Best-in-class well-being programs - Annual, no-cost health assessment program Blueprint for Wellness® - healthyMINDS mental health program - Vacation and Health/Flex Time - 6 Holidays plus 1 "MyDay" off - FinFit financial coaching and services - 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service - Employee stock purchase plan - Life and disability insurance, plus buy-up option - Flexible Spending Accounts - Annual incentive plans - Matching gifts program - Education assistance through MyQuest for Education - Career advancement opportunities - And so much more! Company Description Quest Diagnostics honors our service members and encourages veterans to apply. While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume. Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.

Role Description Liberty Solutions has a client in need of a CDI Coding Analyst. This resource will serve as a CDI coder on the client's internal team, supporting clinical documentation integrity efforts and ensuring accurate, complete, and compliant documentation that reflects patient severity, risk, and quality of care. The initial contract is 3-6 months and then will convert to a permanent FTE role. Resources must have active CCS and CCDS credentials from AHIMA or AAPC and cannot be located in California, New York, Colorado, or Washington. Qualifications - 4+ years of experience serving as a CDI coder - Strong knowledge of DRG payor methodologies, including MS-DRG and APR-DRG - Proficiency with ICD-10-CM and ICD-10-PCS coding guidelines and conventions - Working knowledge of PSIs, HACs, HCCs, and Medicare IPPS - Demonstrated experience writing compliant coding queries - Experience bridging CDI and coding functions, including DRG reconciliation - Prior experience working with Cerner clients required - Clinical background preferred (RN, LPN, or other clinical licensure) Requirements - Candidates must hold the following active credentials from AHIMA or AAPC (CCS and CCDS); multiple certifications are strongly preferred - Certification Requirements: - CCS (Certified Coding Specialist) - CCDS (Certified Clinical Documentation Specialist) - Candidates with the following certifications (in addition to the above) would be a big plus: - RHIA (Registered Health Information Administrator) - RHIT (Registered Health Information Technician) - CIC (Certified Inpatient Coder) - CDIP (Certified Documentation Integrity Practitioner) - CCDS-O (Certified Clinical Documentation Specialist – Outpatient) - All credentials must be current and in good standing. Candidates with a stacked CDI and coding credential profile (e.g., CCS + CCDS) will be prioritized. Company Description Liberty Solutions, Inc. has been a leader in the Healthcare IT industry for over a decade, providing innovative solutions that help our clients thrive. Our commitment to excellence and customer satisfaction has earned us a loyal clientele, and our employees enjoy a collaborative and supportive work environment. This is a remote position.

As a global leader in cybersecurity, CrowdStrike protects the people, processes and technologies that drive modern organizations. Since 2011, our mission hasn’t changed — we’re here to stop breaches, and we’ve redefined modern security with the world’s most advanced AI-native platform. Our customers span all industries, and they count on CrowdStrike to keep their businesses running, their communities safe and their lives moving forward. We’re also a mission-driven company. We cultivate a culture that gives every CrowdStriker both the flexibility and autonomy to own their careers. We’re always looking to add talented CrowdStrikers to the team who have limitless passion, a relentless focus on innovation and a fanatical commitment to our customers, our community and each other. Ready to join a mission that matters? The future of cybersecurity starts with you. About the Role: CrowdStrike is looking for highly motivated, self-driven, technical analysts dedicated to making a difference in global security by protecting organizations against the most advanced attackers in the world. Our CrowdStrike virtual security operations center offers opportunities to expand your skill set through a wide variety of experiences, detecting and responding to incidents as they occur in real-time for our customers. - Do you find yourself interested in putting your hands-on technical skills to the test in detecting, containing, and remediating incidents? - Are you self-motivated and looking for an opportunity to rapidly accelerate your skills? - Do you crave new and innovative work that actually matters to your customer? - Do you have an Incident Response or Information Security background that you’re not fully utilizing? - Are you capable of leading teams and interacting well with customers? - Do you love working around like-minded, smart people who you can learn from and mentor on a daily basis? What You'll Do: - Conduct monitoring and perform in-depth analysis of security alerts. - Exercise incident handling processes across Windows, Mac, and Linux platforms. - Perform malware analysis. - Perform remote remediation of malware or malicious activity. - Develop and improve processes for incident detection, triage, and the execution of countermeasures - Produce high-quality written and verbal communications, recommendations, and findings to customer management. - Demonstrate industry thought leadership through blog posts, CrowdCasts, and other public speaking events. - Manage internal programs or teams. - Serve as the technical escalation point and mentor for lower-level analysts. - Provide oversight and quality assurance for issues worked by lower-level analysts. - Assist in the advancement of security processes and procedures. What You'll Need: Successful candidates will have experience in one or more of the following areas: - Incident Handling: experience conducting or managing incident response for organizations, investigating targeted threats such as the Advanced Persistent Threat, Organized Crime, and Hactivists. - Computer Forensic Analysis: a background using a variety of forensic analysis tools in incident response investigations to determine the extent and scope of compromise. - Systems Administration: an understanding of system internals is required to understand how to implement and execute countermeasures and remediation. - Network Forensic Analysis: knowledge of network protocols, network analysis tools, and ability to perform analysis of associated network logs. - Malware Analysis: ability to perform static and dynamic malware analysis to understand the nature of malware - Incident Remediation: strong understanding of targeted attacks and able to create customized tactical and strategic remediation plans for compromised organizations. - Network Operations and Architecture/Engineering: strong understanding of secure network architecture and strong background in performing network operations. - Programming/Scripting: experience coding in Powershell, C, C#, VB, Python, Perl, Ruby on Rails, and.NET. Education: BA or BS / MA or MS degree in Computer Science, Computer Engineering, Math, Information Security, Information Assurance, Information Security Management, Intelligence Studies, Cybersecurity, Cybersecurity Policy, or a related field. Bonus Points: - 4-6 years of relevant incident handling experience - At least one relevant security certification - Strong verbal and communication skills - Strong problem solving skills - Strong experience with Mac OS, Windows, and Unix operating systems. - Ability to handle high pressure situations in a productive and professional manner. - Strong time management skills with the ability to multi-task #LI-EV1 #LI-Remote #LI-JP1 Benefits of Working at CrowdStrike: - Market leader in compensation and equity awards - Comprehensive physical and mental wellness programs - Competitive vacation and holidays for recharge - Paid parental and adoption leaves - Professional development opportunities for all employees regardless of level or role - Employee Networks, geographic neighborhood groups, and volunteer opportunities to build connections - Vibrant office culture with world class amenities - Great Place to Work Certified™ across the globe CrowdStrike is proud to be an equal opportunity employer. We are committed to fostering a culture of belonging where everyone is valued for who they are and empowered to succeed. We support veterans and individuals with disabilities through our affirmative action program. CrowdStrike is committed to providing equal employment opportunity for all employees and applicants for employment. The Company does not discriminate in employment opportunities or practices on the basis of race, color, creed, ethnicity, religion, sex (including pregnancy or pregnancy-related medical conditions), sexual orientation, gender identity, marital or family status, veteran status, age, national origin, ancestry, physical disability (including HIV and AIDS), mental disability, medical condition, genetic information, membership or activity in a local human rights commission, status with regard to public assistance, or any other characteristic protected by law. We base all employment decisions--including recruitment, selection, training, compensation, benefits, discipline, promotions, transfers, lay-offs, return from lay-off, terminations and social/recreational programs--on valid job requirements. If you need assistance accessing or reviewing the information on this website or need help submitting an application for employment or requesting an accommodation, please contact us at recruiting@crowdstrike.com for further assistance.

Role Description The Senior Quality Assurance Analyst (Regulatory Affairs) is responsible for driving quality and compliance excellence across Intelerad’s Software as a Medical Device (SaMD) portfolio. This role combines deep knowledge of medical device quality systems with hands-on execution of core QA/RA processes, including CAPA, audit readiness, supplier oversight, and regulatory support. As a senior individual contributor within the Regulatory Affairs & Quality organization, this role partners cross-functionally to ensure quality and regulatory requirements are embedded throughout the product lifecycle and that Intelerad maintains a state of continuous compliance. Key Responsibilities - Quality System Execution & Continuous Improvement - Lead and manage Corrective and Preventive Actions (CAPAs), including investigations, root cause analysis, effectiveness checks, and documentation. - Drive improvements to the Quality Management System (QMS) in alignment with ISO 13485, FDA 21 CFR Part 820, and applicable global regulations. - Author, review, and maintain quality system documentation, including SOPs, work instructions, and forms. - Track, trend, and analyze quality metrics to identify systemic issues and improvement opportunities. - Collaborate with development teams in an Agile environment to integrate quality practices throughout the software development lifecycle. - Participate in continuous learning opportunities including training and conferences to stay current with QA methodologies, emerging technologies, and industry best practices. - Audit & Inspection Readiness - Lead and support internal audits to ensure ongoing compliance with regulatory and internal requirements. - Support external audits and inspections (e.g., FDA, Notified Bodies, Health Canada). - Coordinate timely responses to audit findings and ensure effective remediation and closure. - Supplier & Vendor Quality Management - Lead supplier qualification, evaluation, and monitoring activities. - Ensure supplier compliance with quality agreements and regulatory expectations. - Support supplier audits and ongoing performance assessments. - Regulatory Support - Support preparation and maintenance of regulatory submissions and registrations for global markets. - Participate in regulatory impact assessments, change control, and product lifecycle activities. - Collaborate with Regulatory Affairs leadership to support global compliance strategies. - Cross-Functional Collaboration - Partner with R&D, Product, Clinical, and Operations teams to integrate quality and regulatory requirements into development and operational processes. - Provide guidance on risk management (ISO 14971) and design control expectations. - Support complaint handling, post-market surveillance, and vigilance activities. Qualifications - Bachelor’s degree in a scientific, engineering, or healthcare-related field, or equivalent industry experience. - 4+ years of experience in Quality Assurance and/or Regulatory Affairs within the medical device industry. - Demonstrated experience working within a certified Quality Management System (ISO 13485). - Strong working knowledge of: - FDA 21 CFR Part 820 / QSR (and QMSR readiness). - ISO 13485. - ISO 14971 risk management principles. - Proven experience managing CAPA, audits, and supplier quality processes. Requirements - Strong analytical and problem-solving skills. - Ability to lead quality initiatives and influence cross-functional stakeholders. - Excellent written and verbal communication skills. - Strong organizational skills with the ability to manage multiple priorities. - Ability to work independently in a regulated, fast-paced environment. Benefits - Experience with electronic QMS platforms (e.g., Greenlight Guru or similar). - Prior experience supporting regulatory inspections. - Familiarity with global regulatory frameworks (EU MDR, UKCA, Health Canada, TGA, etc.). - Quality certifications (e.g., ASQ CQE, CQA). - Experience with Software as a Medical Device (SaMD) or healthcare software a major bonus.