1,224 vagas para regulatory affairs manager em todo o país.

Senior Regulatory Affairs & Labeling Manager (m/f) Referencia: JN -102026-7128013 Adicionado em 19.10.2026 Sobre os nossos clientes Our client is a global healthcare company committed to improving access to high-quality medicines and healthcare solutions worldwide. Focused on improving patients' lives, the company delivers ...

... English. Job Offer - Exposure to international stakeholders and strategic projects. - Collaborative and innovative working environment. Apply to discuss this Regulatory Information Management (Rim) - Associate Manager role in more detail O que procuramos Regulatory Information Management; RIM; Regulatory Affairs; Assuntos ...

... atrativas - Políticas work-life balance - Desenvolvimento contínuo - Ambiente de trabalho dinâmico e colaborativo #LI-CN1 Required skills: Business Opportunities, Communication, Decision Making, Documentations, External Relations, Institutional Relations, Internal Processes, Regulatory Coordination, Regulatory Engagement []

... Partner closely with Regulatory Affairs, Medical Affairs, Quality, Supply Chain, Launch Management and Legal teams to ensure seamless end-to-end execution from regulatory approval through artwork implementation and market release. - Drive continuous improvement initiatives, maintain awareness of emerging regulatory requirements, ...

... Partner closely with Regulatory Affairs, Medical Affairs, Quality, Supply Chain, Launch Management and Legal teams to ensure seamless end-to-end execution from regulatory approval through artwork implementation and market release. - Drive continuous improvement initiatives, maintain awareness of emerging regulatory requirements, ...

... development, quality control, and delivery, in conjunction with product and technical teams - Lead requirements gathering sessions with client business, IT, Regulatory Affairs, and Quality stakeholders to define and document business needs - Create detailed specifications and solution designs, documenting current and future ...

IQVIA seeks a Regulatory Affairs Specialist to support clinical development projects across Europe, with focus on EU Clinical Trials Regulation submissions. The role involves independent management of regulatory activities, protocol review, and cross-functional collaboration for drug development programs including small ...

We are looking for a Regulatory Affairs professional to join our IQVIA Biotech Regulatory Affairs team, supporting clinical research projects across Europe. In this role, you will provide regulatory expertise and hands-on support throughout clinical development, with a particular focus on EU Clinical Trials Regulation (EU ...

O nosso cliente atua como consultora para a indústria farmacêutica. No âmbito da sua estratégia de crescimento, pretende reforçar a sua estrutura no Estoril com um(a) Regulatory Affairs Associate. []

Reporting to the Clinical Research Country Lead, an exciting opportunity has arisen for a Clinical Operations Manager . This position is responsible for ensuring the performance, compliance, and execution of assigned clinical trial protocols within the country, in accordance with ICH-GCP guidelines, local regulatory requirements, ...

... suitability and quality risks. - Ensures timely submission of application/documents to EC/IRB at start up and for the duration of the study. Works together with Regulatory Affairs to ensure timely delivery of application/documents for submissions to Regulatory Authority for the duration of the study, and in line with local regulations. ...

... January 2027 - Duration: 12 months - Work mode: full time, hybrid (3 days onsite) About the job As a Medical Affairs Trainee , you will support the Medical Affairs team in Portugal in bridging scientific evidence and clinical practice. You will gain hands-on experience in medical affairs, medical communication, evidence ...

... with In International Operations, colleagues work across markets to serve people around the world and help improve health at scale. You will join Medical & Regulatory in Portugal. Your closest partners will be Medical Affairs, Regulatory Affairs, Safety, Quality, Marketing, Sales and Communication/Corporate Affairs, alongside ...

... skills and a commitment to code quality and knowledge sharing. Nice to Have - Previous experience in investment banking or financial markets . - Exposure to regulatory reporting or regulatory IT systems. - Experience with automated testing and continuous integration practices. - Knowledge of financial data integration and ...

... quality reviews, regulatory controls, and root cause analysis for reporting breaches. - Collaborate with internal stakeholders, IT teams, and international regulatory reporting teams to resolve issues and implement improvements. - Produce KPIs, management reports, and regulatory reporting metrics while maintaining procedures ...

... worldwide operations. Apply to discuss the Regulatory Information Management (Rim) Specialist role in more detail. O que procuramos Veeva RIM; RIM Systems; Regulatory Systems; Data Governance; Data Quality; eCTD; Electronic Submissions; Regulatory Affairs; Regulatory Information Management (RIM); Regulatory Operations Contacto ...

... Collaborative and multicultural working environment. Apply to discuss the Senior Regulatory Operations Specialist - Electronic Submissions role. O que procuramos Regulatory Operations; Regulatory Publishing; eCTD Publishing; Veeva Vault; Regulatory Affairs Contacto da Michael Page Clique aqui para responder a este anúncio. []

... products and services in compliance with applicable regulatory frameworks; - Coordinate responses to regulatory inquiries, audits, and consultations; - Track regulatory developments across the EU and provide strategic advice on their business impact; - Engage with regulatory authorities and contribute to responses to public ...

... all applications and next steps. Our partner is looking for a Web3 Licensing and Regulatory Compliance Specialist based in Portugal. The Web3 Licensing and Regulatory Compliance Specialist will support digital-asset businesses in navigating complex regulatory frameworks and obtaining the authorizations required to operate. ...

... This role will be based in Lisbon. This is a hybrid role that has a requirement of working at least three days a week in the office. Marsh’s Cyber Risk and Regulatory Compliance team helps clients identify, assess and manage cyber and technology-related risks that can disrupt business operations, including ransomware, data ...