Regulatory Affairs Manager

hace 2 semanas


Municipio de Esquel, Argentina Kaizen Gaming A tiempo completo

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



  • Municipio de Cañada de Gómez, Argentina Fullscript A tiempo completo

    A health tech company in Argentina is seeking a Quality & Regulatory Affairs Manager to ensure compliance with FDA and Health Canada regulations. The role includes managing licensing and documentation, supporting audits, and maintaining product quality across a dynamic environment. Candidates should have 5+ years of experience in regulatory affairs and a...


  • Municipio de Cañada de Gómez, Argentina Fullscript A tiempo completo

    A health tech company in Argentina is seeking a Quality & Regulatory Affairs Manager to ensure compliance with FDA and Health Canada regulations. The role includes managing licensing and documentation, supporting audits, and maintaining product quality across a dynamic environment. Candidates should have 5+ years of experience in regulatory affairs and a...


  • San Miguel de Tucumán, Argentina Fullscript A tiempo completo

    Quality & Regulatory Affairs Manager Join to apply for the Quality & Regulatory Affairs Manager role at Fullscript. About Fullscript Founded in 2013, Fullscript started 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 a health intelligence...


  • Municipio de Avellaneda, Argentina Johnson & Johnson Innovative Medicine A tiempo completo

    Experienced Regulatory Affairs Specialist Join us as an Experienced Regulatory Affairs Specialist based in Buenos Aires, Argentina or Santiago, Chile. You will be responsible for end‑to‑end regulatory lifecycle management of labeling updates across Argentina, Chile, Uruguay, Paraguay, and Bolivia. Purpose Execute the complete labeling lifecycle...


  • Municipio de Neuquén, Argentina Fullscript A tiempo completo

    About Fullscript Founded in ****, Fullscript started 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 a health intelligence platform that powers every part of care. Today, 125,000 practitioners rely on Fullscript for clinical insights, lab...


  • Municipio de Cañada de Gómez, Argentina Fullscript A tiempo completo

    About Fullscript Founded in 2011, Fullscript started 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 a health intelligence platform that powers every part of care. Today, 125,000 practitioners rely on Fullscript for clinical insights, lab...


  • Municipio de Esquel, Argentina Syneos Health A tiempo completo

    Regulatory Labeling Manager (NA and LATAM Only) Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to...

  • Remote Regulatory

    hace 1 semana


    Municipio de Neuquén, Argentina Fullscript A tiempo completo

    A health intelligence platform provider is seeking a Quality & Regulatory Affairs Manager to ensure compliance with dietary supplement regulations. The role involves collaboration across teams, managing regulatory documentation, and maintaining compliance standards. The ideal candidate will have over 5 years of experience in regulatory affairs, knowledge of...

  • Remote Regulatory

    hace 2 semanas


    Municipio de Neuquén, Argentina Fullscript A tiempo completo

    A health intelligence platform provider is seeking a Quality & Regulatory Affairs Manager to ensure compliance with dietary supplement regulations. The role involves collaboration across teams, managing regulatory documentation, and maintaining compliance standards. The ideal candidate will have over 5 years of experience in regulatory affairs, knowledge of...

  • Remote Regulatory

    hace 1 semana


    Municipio de Resistencia, Argentina Fullscript A tiempo completo

    A health intelligence company in Resistencia, Argentina, is looking for a Quality & Regulatory Affairs Manager to ensure compliance with dietary supplement regulations. The candidate should have over 5 years of experience in regulatory affairs, a Bachelor’s degree in a related field, and excellent communication skills. This is a hands-on role requiring...