Role Description Now we are scaling globally and we are looking for a Compliance Analyst who feels comfortable working in a challenging and dynamic environment, has strong attention to detail and the ability to see the bigger picture. - Review user transaction documents and provide support with compliance issues. - Conduct analysis and manage alerts generated by monitoring systems. - Assist with compliance due diligence, including KYC (Know Your Customer) and AML (Anti-Money Laundering) tasks. - Act as a primary point of contact for users regarding compliance-related materials and issues. - Assist in researching and responding to comments and inquiries from foreign regulators. - Provide feedback on ways to improve operational and technological aspects of compliance operations. - Use your English communication skills for both verbal and written interactions. - Demonstrate accountability, ethics, and integrity in all aspects of your role. Qualifications - Advanced student or graduate in Law, Accounting, Business Administration, Economics, or a related field. - Minimum of 2 years of experience in related roles. - Proficiency in written and spoken English. - Strong communication skills. - Excellent analytical and problem-solving abilities. Requirements - Understanding of AML/CFT (Counter Financing of Terrorism) and sanctions risks. - Experience with U.S. compliance regulations. - Experience with regulatory and compliance matters in international markets (e.g., Asia, Africa, Europe). Benefits - Contractor modality with global compensation. - PTO & holidays. - Office lunch. - Culture & hubs: a young, high-performance team based in San Francisco, Buenos Aires, Bogotá, or remote. - High impact & exponential growth: full autonomy to lead; your limits are defined by your ambition.

• Be exposed to the broad scope of global Regulatory Affairs and specifically CMC Regulatory Affairs and the role’s contribution to drug development and patients’ access to medicines. • Learn about the role of global Health Authorities in the drug development process. • Gain hands-on experience in preparing regulatory documents for submission to global health authorities. • Acquire knowledge about the differences in regulatory requirements across regions. • Experience CMC technical product development and manufacturing functions in relation to regulatory affairs. • Responsible for maintaining accurate CMC information in the BeOne Regulatory Information Management system. • Data remediation. • Create and maintain CMC Submission Content. • Upload HA Correspondence/HA Questions/Commitments. • Maintain internal Regulatory CMC trackers. • Contribute to Reg CMC process improvements. • Support the drafting of CTD CMC sections to ensure on-time and high-quality global applications for direct submission to Health Authorities as needed. • Provide support to Reg CMC team or hiring manager with Regulatory submissions and other tasks as needed.

• Evaluating Government Program (Medicare and Medicaid) regulations and contracts • Managing direct reports and providing oversight of operational compliance • Developing policies, conducting monitoring, managing risk • Acting as a liaison with regulatory agencies to prevent legal penalties • Identifying risks and developing remediation strategies • Working with Corporate Compliance and business personnel • Providing compliance consultation and guidance to business owners

Role Description As a Staff Global Regulatory Affairs, you will ensure that Beckman Coulter products, processes, and documentation adhere to global premarket regulations for registration lifecycle management, global labeling requirements, and marketing material review and approval procedures. This position reports to the Director of Global Compliance and Regulatory Affairs and is part of the Global Regulatory Affairs Department and will be fully remote. In this role, you will have the opportunity to: - Develop, implement and execute global regulatory strategies to ensure worldwide compliance through standardized processes and procedures and support internal and external audits and regulatory inspections. - Manage, maintain and optimize tools and workflows used to manage the product regulatory lifecycle. - Develop and manage BEC global regulatory product labeling requirements and procedures. - Manage the regulatory requirements for the content of marketing, advertising, promotional, and sales product training and scientific material (MAPSS) and ensure global registration activities align with applicable regulatory requirements. - Build strong partnerships with Business Unit Regulatory Affairs and Commercial Regulatory Affairs teams, sharing best practices and driving cross-functional initiatives. Qualifications - Bachelor’s degree in applicable fields (such as biological sciences, biomedical engineering, or chemistry) with 9+ years of related work experience OR Master's degree in applicable field with 7+ years of related work experience OR Doctoral degree in applicable field with 4+ years of related work experience. - Critically review global regulations and evaluate applicability and impact to BEC products and processes. - Develop clear written assessments and stakeholder-ready presentations to communicate regulatory requirements and recommendations. - Microsoft tool proficiency. Requirements - Ability to periodically travel to the US (minimum once a year). - Prior experience with in-vitro diagnostic devices or other regulated industries. - Leads effectively in matrixed and cross-cultural environments, driving timely decisions, issue resolution, and resource agility while setting high expectations and modeling accountability and integrity. - Communicates complex and sensitive information clearly across diverse audiences; builds consensus, demonstrates strong writing and documentation skills, and uses sound judgment to influence and lead through change. Benefits - Comprehensive package of benefits including paid time off, medical/dental/vision insurance, and 401(k) to eligible employees. - Annual salary range for this role is $140,000 - 170,000. - This job is also eligible for bonus/incentive pay.