• Serve as the primary point of contact for customs inquiries from internal teams, brokers, and authorities • Perform Harmonized Tariff classification and manage preferential origin determination • Monitor regulatory changes and conduct regular audits for compliance • Review supply chain changes and new product launches for risk evaluations and duty savings • Build strong relationships with external partners and deliver training to internal stakeholders

Veterinary Hospital Compliance Manager (remote) Company: Associated Veterinary Partners Position Overview: The Veterinary Hospital Compliance Manager is responsible for developing, implementing, and maintaining compliance programs across all hospitals to ensure adherence to federal, state, and local regulations. This role focuses on regulatory areas including OSHA, DEA/controlled substances, radiation safety, scope of practice, professional licensing, and day care/boarding compliance. The Compliance Manager partners closely with hospital leadership, operations, and medical teams to mitigate risk, close compliance gaps, and standardize processes across the organization. This role requires approximately 50% travel to hospitals to conduct audits, support training, and ensure consistent execution of compliance standards. Key Responsibilities:  Regulatory Compliance Oversight  - Lead compliance efforts across OSHA, DEA (controlled substances), radiation safety, scope of practice, day care/boarding, and state/local regulatory requirements  - Ensure all hospitals maintain current licenses, permits, and registrations  - Monitor regulatory changes and proactively update policies, SOPs, and workflows  Controlled Substance (DEA) Compliance  - Oversee controlled substance policies, storage, logging, and auditing processes  - Conduct routine and random audits  - Investigate discrepancies and implement corrective actions  OSHA & Workplace Safety  - Maintain OSHA-compliant programs  - Track required safety training  - Lead incident reporting and prevention  Radiation Safety  - Ensure compliance with radiation safety standards  - Partner with vendors and regulatory bodies  Licensing, Credentialing & Scope of Practice  - Track all licenses and renewals  - Monitor scope-of-practice requirements  - Ensure workflows remain compliant  Day Care & Boarding Compliance  - Maintain knowledge of state/local regulations  - Ensure compliance with staffing, vaccination, sanitation, and safety standards  - Develop SOPs and conduct audits  Auditing, Field Enablement & Risk Management  - Conduct audits across hospitals  - Develop OSHA, DEA, and boarding checklists  - Train ROMs to conduct audits  - Establish audit cadence and track resolution  Training & Education  - Deliver compliance training  - Create SOPs and toolkits  Cross-Functional Collaboration  - Partner with Operations, Medical Leadership, and HR  - Support M&A integrations  Skills & Competencies: - Strong attention to detail  - Ability to translate regulations into operations  - Strong auditing and coaching skills  - Effective communicator  - Ability to work independently  Success Metrics: - 100% licensing compliance  - No scope-of-practice or boarding compliance gaps  - Consistent ROM audit execution  - New hire training compliance

• Provide expert guidance to Product, Risk, and Operations teams on new product launches, payment flows, and process changes to ensure total alignment with Card Network rules, internal policies, and regulatory standards. • Review and assess new payment products, features, partnerships, and geographic expansions to identify regulatory, financial crime, licensing, and card network compliance implications, and escalate key considerations and recommendations. • Identify, assess, and monitor compliance risks, control gaps, and emerging issues impacting payments activities; document findings and escalate material issues in accordance with established governance and issue escalation protocols. • Draft, maintain, and update payments-related policies, procedures, and standards. • Monitor regulatory developments, card network updates, enforcement actions, and industry trends; communicate relevant changes to impacted stakeholders. • Support third-party due diligence reviews and ongoing monitoring. • Develop, manage and implement effective and ongoing compliance training and educational programs for employees to increase awareness and knowledge of compliance policies and enhance business understanding of related laws and regulatory requirements. • Review alerts and unusual activity related to payments; prepare SAR narratives and supporting investigative documentation for review and submission by the BSA Officer. • Conduct transactions and product risk analysis to identify suspicious activity patterns, emerging typologies, and control weaknesses. • Perform risk assessments and targeted reviews of payments processes to identify vulnerabilities and recommend mitigation actions. • Provide subject matter expertise and day-to-day compliance guidance to business partners to promote consistent understanding of payments compliance requirements. • Monitor regulatory developments and coordinate communication and training to relevant business units. • Perform gap assessments against regulatory expectations, card network rules, Nacha requirements, and industry best practices. • Support compliance monitoring, quality assurance reviews, and remediation of identified issues. • Support ACH, card network, and banking partner audits by preparing documentation, responding to requests, and tracking remediation activities. • Prepare compliance reporting and metrics related to payments compliance activities, including monitoring results, issue remediation status, and regulatory developments.

Title: Sr Reg Affairs Spec Location: Remote Mexico Full time Remote Join Us as a Senior Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years. As part of our global team, you’ll have the opportunity to serve as a senior contact in providing innovative solutions, including regulatory expertise. As a Senior Regulatory Affairs Specialist, you'll interact with clients to provide strategic regulatory intelligence and guidance supporting product development from preclinical stages through registration and product optimization. You will provide strategic, expedient, and efficient preparation of client deliverables that meet current local, regional, and ICH regulatory and technical requirements. Additionally, you will act as a liaison with internal and external clients in the provision and marketing of these services. What You’ll Do: • Prepares and reviews regulatory submissions. • Provides regulatory strategy and/or technical advice to internal and external clients, and acts as a liaison in executing strategies. • Leads the development and implementation of project-specific processes for sponsors. • Collaborates extensively with other departments, regulatory consultants, and regulatory authorities. • Assists in identifying and recognizing out of scope activities in a contract in a timely manner and liaises with other departments to follow through on all aspects of contract modifications. • Provides training and guidance to junior team members as appropriate. • Participates in project launch meetings, review meetings and project team meetings. • Supports business development activities, including project budgeting/forecasting. Education and Experience Requirements: • Bachelor's degree or equivalent and relevant formal academic / vocational qualification • Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 5+ years). In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. Knowledge, Skills and Abilities: • Strong English language (written and oral) communication skills as well as local language where applicable • Solid attention to detail and quality as well as strong editorial/proofreading skills • Strong interpersonal skills to work effectively in a team environment and act as a liaison with other departments • Solid computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies • Solid organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects • Solid negotiation skills • Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables • Solid understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization, licensing, lifecycle management; good knowledge of ICH and other • global regulatory guidelines; basic understanding of a regulatory speciality areas, such as preclinical, clinical, CMC, publishing, etc. • Solid understanding of medical terminology, statistical concepts, and guidelines • Strong analytical, investigative and problem-solving skills • Working knowledge of budgeting and forecasting