Regulatory Affairs Manager
hace 3 semanas
Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 19 markets. We always aim to leverage cutting‑edge technology, providing the best experience to our millions of customers who trust us for their entertainment. Our diverse team of more than 2,700 Kaizeners spans 40+ nationalities across 3 continents. We are proud to be among the Best Workplaces in Europe and certified Great Place to Work at our offices. Ready to press play on potential? Role Overview The Regulatory Affairs Manager will oversee Kaizen Gaming’s regulatory compliance and public affairs strategy, ensuring full adherence to gaming regulations while actively shaping policy at local and international levels. The role serves as the company’s representative to regulators and industry stakeholders, driving compliance and proactively engaging in legislative discussions to protect and promote Kaizen’s interests. Responsibilities Develop and implement Kaizen’s regulatory and public affairs strategy, ensuring compliance with gaming laws while engaging in policy discussions that impact the industry. Represent Kaizen in regulatory and government affairs, fostering transparent relationships with regulators and policymakers and attending industry forums. Monitor regulatory changes, contribute to policy discussions through position papers and consultation responses, and engage in lobbying efforts to support fair and sustainable regulatory frameworks. Develop regulatory messaging aligned with Kaizen’s business goals and oversee Kaizen’s participation in trade associations, contributing to collective regulatory responses and policy recommendations. Qualifications & Experience A minimum of 5+ years in regulatory affairs, public affairs, or compliance, including at least 3 years in a senior role within the gaming or regulated industry. Proven experience in government relations and policy influence across multiple jurisdictions. Deep understanding of gaming regulations and compliance requirements with expertise in political advocacy and stakeholder management. Ability to communicate complex regulatory concepts to diverse audiences, including government officials. Proven ability to lead and mentor teams, build cross‑functional partnerships, and foster a compliance‑driven culture. Exceptional writing, presentation, and negotiation skills, with the ability to draft regulatory responses and influence decision‑makers. Personal Attributes Integrity, discretion, and resilience in handling regulatory challenges. A proactive, adaptable, and strategic thinker with a hands‑on approach to problem‑solving. Perks Hybrid way of working A buddy will support you with your onboarding Competitive pay and bonus scheme Private health insurance for you and your family Monthly meal allowance Commuting allowance Developmental 360° feedback framework Unlimited access to Udemy & continuous training Recruitment Privacy Notice Regarding the data you share with us, you may find and read our recruitment privacy notice here. Equal Opportunity We are an equal opportunity employer committed to fostering a diverse and inclusive workplace. We welcome applications from individuals of all backgrounds, regardless of race, gender, religion, sexual orientation, or age. Seniority level Not Applicable Employment type Full‑time Job function Advertising Services, Media Production, and Online Audio and Video Media Location Buenos Aires, Buenos Aires Province, Argentina #J-18808-Ljbffr
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Hybrid Regulatory Affairs Specialist – Argentina
hace 4 semanas
Municipio de Rincón de los Sauces, Argentina Medtronic A tiempo completoA leading global healthcare technology company is seeking a Regulatory Affairs Specialist in Argentina to manage regulatory submissions, ensure compliance, and liaise with regulatory agencies. The role requires a Bachelor's degree and a minimum of 2 years of experience in the medical devices or pharmaceutical industry. The candidate must be fluent in English...
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Regulatory Affairs Specialist
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Quality & Regulatory Affairs Manager
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Cañada de Gómez, Santa Fe, Argentina Fullscript A tiempo completoAbout FullscriptFounded in ****,Fullscriptstarted by solving one problem: helping practitioners access and prescribe the products they trust to deliver integrative care.What began as a simple solution has evolved into ahealth intelligence platformthat powers every part of care.Today,125,000 practitionersrely on Fullscript for clinical insights, lab...
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LATAM Regulatory Counsel
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