regulatory specialist

A global medical technology company is seeking a Complaint Intake Specialist in Mexico City. This role involves documenting customer-reported product complaints, ensuring regulatory compliance, and supporting the sales team in communications. The ideal candidate has a background in science or engineering and experience in the medical device industry, along...

Omya is seeking a Regulatory Affairs professional to support product registrations and ensure documentation complies with customer and regulatory requirements across markets.The role involves coordinating with innovation teams in Latin America, preparing submissions, and maintaining data integrity in regulatory databases, while ensuring timely and accurate...

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable biosimilar and generic medicines. As we move forward on this new and ambitious path, unique opportunities will arise, both professionally and personally. Join us—the future is in our hands!Major accountabilities:Regulatory Affairs...

About Nubank Nubank was founded in 2013 to free people from a bureaucratic, slow and inefficient financial system. Since then, through innovative technology and outstanding customer service, the company has been redefining people's relationships with money across Latin America. With operations in Brazil, Mexico, and Colombia, Nubank is today one of the...

About NubankNubank was founded in 2013 to free people from a bureaucratic, slow and inefficient financial system. Since then, through innovative technology and outstanding customer service, the company has been redefining people's relationships with money across Latin America. With operations in Brazil, Mexico, and Colombia, Nubank is today one of the...

Job Description SummaryEnsure the timely regulatory maintenance of the assigned portfolio through effective planning and management of regulatory submissions, proactively identifying and mitigating regulatory risks to support the successful approval of submissions and ensure product continuity in the market without regulatory-related disruptions.Job...

Fortrea is seeking a Regulatory Start-up Specialist to act as the local expert for site activation and regulatory submissions. You will collect essential documents, prepare country applications, and liaise with EC/IRB/Regulatory Authorities to meet timelines and sponsor requirements.The role requires 2+ years in clinical research with strong ICH/RA/IRB...

ESSENTIAL FUNCTIONS PERFORMED Collaborates with key stakeholders to ensure alignment of regulatory goals and objectives with the strategic priorities of the business. Develops and maintains strong strategic partnerships with project team members, including Marketing, R&D, Operations, Clinical Affairs and Quality Assurance. Ensures all regulatory activities...

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable biosimilar and generic medicines. As we move forward on this new and ambitious path, unique opportunities will arise, both professionally and personally. Join us—the future is in our hands!Major accountabilities:Regulatory Affairs...

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Fresenius Medical Care, a global leader in kidney care, invites an Regulatory Affairs Expert to join the Reynosa plant in Mexico. You will manage regulatory documentation, support global registrations, ensure compliance, and lead regulatory aspects of product and process changes across the lifecycle.You will collaborate with cross-functional teams to...

Location: Jalisco: Tlajomulco de Zúñiga Post Date: 9/9/2026 Category: Quality Systems Close Date: Employment Type: Regular Summary Regulatory Affairs Specialist performs reviews and audits of certification related documentation, ensuring compliance to all quality management standards, governmental rules, regulations and requirements for the contract...

Summary Regulatory Affairs Specialist performs reviews and audits of certification related documentation, ensuring compliance to all quality management standards, governmental rules, regulations and requirements for the contract manufacturing of products. Fosters divisional teamwork within a continuous improvement environment. Provides regulatory and quality...

Location: Jalisco: Tlajomulco de Zúñiga Post Date: 9/9/2026 Category: Quality Systems Close Date: Employment Type: Regular Summary Regulatory Affairs Specialist performs reviews and audits of certification related documentation, ensuring compliance to all quality management standards, governmental rules, regulations and requirements for the contract...

Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable biosimilar and generic medicines. As we move forward on this new and ambitious path, unique opportunities will arise, both professionally and personally. Join us—the future is in our hands! Major Accountabilities • Regulatory...

Summary Regulatory Affairs Specialist performs reviews and audits of certification related documentation, ensuring compliance to all quality management standards, governmental rules, regulations and requirements for the contract manufacturing of products. Fosters divisional teamwork within a continuous improvement environment. Provides regulatory and quality...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across...

Fortrea is seeking a Regulatory Start-up Specialist to act as the local expert for site activation and regulatory submissions. You will collect essential documents, prepare country applications, and liaise with EC/IRB/Regulatory Authorities to meet timelines and sponsor requirements.The role requires 2+ years in clinical research with strong ICH/RA/IRB...

¿Quieres ser parte del #TeamEvertec? Aquí te contaremos cómo puedes hacerlo👇 🔸Sé parte de un ambiente donde puedas contribuir con tu creatividad, conocimientos y habilidades. Somos la #TecnologíadeloPosible, juntos podemos impulsar la innovación y ser líderes en la industria tecnológica, mientras creamos experiencias excepcionales para...

Alcon MX busca iniciar una trayectoria profesional en Regulatory Operations, dentro de su función de Calidad y Régimen Regulatorio. La persona seleccionada apoyará objetivos de proyecto manejando presentaciones regulatorias, manteniendo bases de datos y asegurando el cumplimiento de normativas externas e internas, con especial atención a dossiers,...