Emprego regulatory affairs Lisboa

What will you do? - Maintenance of the Quality Management System (QMS) and application of the Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) for medicinal gases and Medical Devices; - QMS, GMP, GDP and Medical Devices training to all personnel involved in medicinal product and medical devices activities; - Cooperate in any decision to quarantine or dispose of...

O Laboratório Edol, empresa do Grupo Faes Farma, pretende reforçar a sua equipa de Assuntos Regulamentares com um Técnico de Assuntos Regulamentares – Mercado Nacional & Exportação (Regulatory Affairs Specialist) , para as suas instalações de Carnaxide. Esta vaga será para substituição de uma licença de maternidade. Principais funções/responsabilidades da posição: - Preparação, submissão e...

Tecnimede Group is a Portuguese multinational company, with more than 40 years of history in the life cycle of the drug product for human use - development, production, promotion and marketing - with the mission to improve and preserve the human life and the human health. Exporting to more than 100 countries worldwide, it is present in 6 countries (Portugal, Spain, Italy, Marocco, Columbia and...

Environmental Resources Management (ERM) is seeking an experienced Plant Protection Regulatory Affairs professional to join us as a Project Manager in Southern Europe. This is a great opportunity to join a global consultancy with a strong track record of advising clients in the chemical sector, with a focus on agrochemicals, biocides and REACH, to help them navigate the complexities of the EU...

Location: Lisbon, Portugal (Hybrid options available) About UpHill At UpHill, we’re on a mission to revolutionize healthcare. By developing best-practice clinical pathways and care orchestration software, we help healthcare providers and life sciences companies across Europe streamline their processes, eliminate inefficiencies, and increase care coordination, which results in improve outcomes...

Shape the future of science with AstraZeneca! We are a global, science-led, patient-focused biopharmaceutical company transforming ideas into life-changing medicines. In Portugal, our purpose is to advance clinical practice and reduce the burden of chronic diseases and cancer by facilitating patient access to innovation—raising awareness, supporting early identification of symptoms, and helping...

The Analyst in Regulatory Affairs will support the monitoring, analysis, interpretation, and implementation of policy and regulatory developments affecting the energy sector. This position involves preparing analytical materials and presentations, providing regulatory insights to guide strategic decisions, and ensuring alignment with evolving EU and national regulatory frameworks. Key...

Renewables regulatory affairs, market and settlement position page is loaded## Renewables regulatory affairs, market and settlement positionlocations: Portugal, Lisboaposted on: Publicado hoytime left to apply: Fecha final: 31 de enero de 2026 (Quedan más de 30 días para realizar la solicitud)job requisition id: R-24468OBJETIVO:Com presença em todas as etapas do projeto (estratégia,...

Join to apply for the Regulatory Affairs Trainee role at GSK Join to apply for the Regulatory Affairs Trainee role at GSK Get AI-powered advice on this job and more exclusive features. Site Name: Lisbon Posted Date: Jun 30 2025 A GSK é uma companhia farmacêutica global, impulsionada pela ciência, com um propósito especial: ajudar as pessoas a fazerem mais, sentirem-se melhor e viverem mais...

Pama Reis Consulting está a reforçar a sua equipa de Regulatory Affairs. Procuramos um(a) Farmacêutico(a) Júnior para integrar a nossa equipa de Regulatory Affairs e desenvolver uma carreira numa área estratégica, exigente e em constante evolução. O que procuramos - Mestrado Integrado em Ciências Farmacêuticas - Interesse pela área de Regulatory Affairs - Boa capacidade de comunicação e inglês...

Regulatory Affairs Study Start Up Specialist II (RASSU) Join to apply for the Regulatory Affairs Study Start‑Up Specialist II (RASSU) role at CTI Clinical Trial and Consulting Services. Responsibilities - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements...

A global leader in business technology is seeking a Regulatory Associate to join their team in Portugal. The role involves analyzing regulatory compliance in e-invoicing, creating relevant content, and collaborating with stakeholders for market integration. Ideal candidates will have 1-3 years of relevant experience and a degree in Business, Law, or Economics, along with excellent communication...

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and...

Location: Porto Salvo Start date: 1st March 2026 Duration: 1 Year Work Model: Hybrid – 3 days per week in the office (Monday or Friday mandatory, Wednesday recommended) About the job As a Regulatory Affairs Trainee, you will support the team in preparing submissions, managing regulatory documents, and maintaining databases. You will collaborate with colleagues across functions, gaining hands-on...

A leading healthcare technology company in Lisbon is seeking a Regulatory Affairs Specialist to develop and manage the regulatory and quality framework. You will ensure compliance with essential regulations like EU MDR and ISO 13485. The ideal candidate will have over 3 years of experience in a medical device setting and must be comfortable collaborating with engineering and product teams. This...

What will you do? - Maintenance of the Quality Management System (QMS) and application of the Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) for medicinal gases and Medical Devices; - QMS, GMP, GDP and Medical Devices training to all personnel involved in medicinal product and medical devices activities; - Cooperate in any decision to quarantine or dispose of...

Tecnimede Group is a Portuguese multinational company, with more than 40 years of history in the life cycle of the drug product for human use - development, production, promotion and marketing - with the mission to improve and preserve the human life and the human health. Exporting to more than 100 countries worldwide, it is present in 6 countries (Portugal, Spain, Italy, Marocco, Columbia and...

O Laboratório Edol, empresa do Grupo Faes Farma, pretende reforçar a sua equipa de Assuntos Regulamentares com um Técnico de Assuntos Regulamentares – Mercado Nacional & Exportação (Regulatory Affairs Specialist) , para as suas instalações de Carnaxide. Esta vaga será para substituição de uma licença de maternidade. Principais funções/responsabilidades da posição: - Preparação, submissão e gestão...

A leading biopharmaceutical company in Portugal is seeking a Medical Information & Regulatory Affairs Specialist. This role involves developing balanced medical information for healthcare professionals and managing inquiries. Candidates must hold a PhD or Master's and have at least 2 years of experience in the pharmaceutical industry. The position demands excellent communication skills in English...

A leading renewable energy firm in Lisbon is seeking an Analyst in Regulatory Affairs to support monitoring and analysis of energy-related legislation. Responsibilities include preparing reports, engaging with stakeholders, and ensuring alignment with regulations. The ideal candidate has a bachelor's degree, 2-3 years of experience in regulatory affairs, and proficiency in Microsoft tools. The...