• Own, advance, and champion Blink's enterprise Compliance Program, including the code of conduct, conflicts-of-interest, gifting, and whistleblower/reporting frameworks. • Lead the established compliance operating cadence (including weekly compliance reviews and the compliance committee), maintaining clear action items, accountability, and follow-through. • Provide periodic reports to the Deputy General Counsel and General Counsel on the nature, progress, and status of the program and emerging risks. • Own the HIPAA compliance program — policies, procedures, authorizations, revocation processes, and recordkeeping — keeping it current and continuing to strengthen it as the business and regulations evolve. • Maintain and enhance the practical guardrails and job aids that help Data, Engineering, and IT teams handle PHI correctly (e.g., approved-vs-not-approved platforms for PHI, data-governance guidance, BAA tracking with vendors). • Monitor and operationalize evolving privacy and consumer-protection requirements, including HIPAA, FTC, and state privacy laws. • Investigate and document potential compliance and privacy concerns, including HIPAA incidents and unauthorized-disclosure events, and partner with stakeholders to develop and execute remediation, coaching, and corrective-action plans. • Manage intake and response for medical-records and legal-process requests in coordination with Legal Operations. • Cooperate with internal and external auditors and reviewers, and lead Blink's responses to security and compliance audits and certifications (e.g., SOC 2, HITRUST) and to client/partner audits of Blink. • Support responses to regulator and state Attorney General inquiries in partnership with Legal. • Manage consumer and patient complaints, patient requests to access or delete information and other privacy-rights requests, and state Attorney General consumer-protection complaints, escalating to Legal where matters become formal enforcement. • Administer Blink’s exclusion and sanctions screening program (OIG/SAM/OFAC), including supporting screening-tool implementation and the investigation of potential screening hits, in partnership with the People team. • Partner with Pharmacy Operations and Clinical teams on quality and error-handling processes (e.g., fulfillment-error review, clinical templates and calibration) and support adverse-event reporting and pharmacovigilance policy. • Support compliance for patient-assistance and manufacturer-sponsored programs, including enrollment/unenrollment processes. • Oversee compliance education and training for all Blink employees, including developing training content and curricula. • Collaborate cross-functionally to determine, document, and implement policies and standard operating procedures that support a culture of compliance. • Support special projects and broader Legal team initiatives as the team and company grow.

• Own and maintain Worth’s compliance and governance programs across AML/BSA, KYB/KYC, OFAC/sanctions, FCRA, privacy, and applicable financial services regulations • Lead and mature the company’s GRC function, including risk assessments, policy governance, control management, audit readiness, and compliance documentation • Support and manage external audits, certifications, and regulatory initiatives including SOC 2, PCI DSS, GDPR/privacy-related obligations, customer due diligence reviews, and emerging AI governance or assurance frameworks as the company and regulatory landscape evolve • Serve as a compliance advisor to Product and Engineering teams to ensure regulatory and governance requirements are embedded into platform capabilities and workflows • Develop and maintain Worth’s AI governance framework, including oversight of AI usage, model governance, data handling, automated decisioning considerations, and emerging AI regulatory requirements • Monitor regulatory developments and translate evolving requirements into actionable operational and product guidance • Act as a primary point of contact for enterprise customers, auditors, and partners on compliance, governance, and regulatory matters • Oversee third-party compliance and risk management processes for vendors, data providers, and technology partners • Lead compliance-related incident response activities, including regulatory inquiries, customer escalations, and coordination on privacy or security events • Own and mature Worth’s third-party risk management program, including compliance oversight, due diligence, ongoing monitoring, and risk assessments for vendors, data providers, technology partners, and other third parties supporting regulated operations • Build compliance awareness and training programs across the organization and help foster a strong culture of governance and accountability

• Oversee the day-to-day operations of the enterprise compliance audit and monitoring program. • Manage risk-based audit programs focused on coding, billing, documentation integrity, and regulatory compliance. • Monitor high-risk billing and operational areas. • Develop audit methodologies, sampling protocols, and documentation standards. • Identify and assess enterprise compliance risks related to federal and state healthcare regulations. • Collaborate with Coding Compliance Educators and CDOCs to develop targeted education initiatives. • Supervise and mentor compliance audit personnel and operational compliance staff as assigned.

Role Description The Quality Compliance Manager (Part-Time) is responsible for maintaining and continuously improving the German Quality Management System (QMS), ensuring compliance with German and EU pharmaceutical regulations. The role oversees quality processes, inspections, audits, training, supplier qualification, CAPA management, and quality oversight of external partners to ensure the organization remains inspection-ready and fully compliant with GxP requirements. Key Responsibilities - Maintain and continuously improve the local Quality Management System (QMS). - Manage quality documentation, including SOPs, forms, records, and periodic reviews. - Coordinate employee training, qualification programs, and compliance records. - Lead supplier, customer, and service provider qualification activities. - Plan, conduct, and follow up on internal audits and quality assessments. - Manage deviations, quality events, CAPAs, and process improvement initiatives. - Oversee quality-related interfaces with manufacturers, external service providers, and batch release partners. - Prepare for, coordinate, and support regulatory authority inspections while ensuring ongoing inspection readiness. Qualifications - Degree in Pharmacy, Life Sciences, or a related scientific discipline. - Minimum 5-7 years of experience in pharmaceutical or healthcare quality management systems. - Experience as a Responsible Person for Wholesale Distribution under German Medicines Act (AMG §52a). - Strong knowledge of GxP requirements, German pharmaceutical regulations, and EU compliance standards. - Manage multiple quality activities, and effectively interact with internal and external stakeholders. Employment Type - Part-Time | Remote (Germany-based)