Emprego regulatory affairs

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...

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...

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...

A leading pharmaceutical company is seeking an Administrative Assistant to support their Regulatory Affairs Department in Portugal. The successful candidate should have strong organizational skills, experience in handling regulatory documentation, and the ability to manage multiple tasks effectively. Responsibilities include submitting variations on the NCA portal, organizing files, and...

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...

A leading global pharmaceutical company in Porto Salvo is seeking an Administrative Assistant to support the Regulatory Affairs Department. The role involves managing documentation, supporting regulatory submissions, and providing logistical support to the team. Ideal candidates will have strong organizational skills, fluency in English, and previous administrative experience in a regulatory or...

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...

A global pharmaceutical company in Porto Salvo seeks an Administrative Assistant for its Regulatory Affairs Department. The role involves providing essential administrative support, managing documentation and submissions, and maintaining regulatory files. Suitable candidates will have prior administrative experience, excellent organizational skills, and the ability to manage multiple priorities...

Apply now » Administrative Assistant - Regulatory Affairs Date: Jan 13, 2026 Location: Porto Salvo, Portugal, 2740-245 Company: Teva Pharmaceuticals Job Id: 65854 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse...

Administrative Assistant - Regulatory Affairs Date: Jan 13, 2026 Location: Porto Salvo, Portugal, 2740-245 Job Id: 65854 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities 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...

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 biopharma company is seeking a Regulatory Affairs Trainee in Lisbon to support regulatory processes. You will prepare submissions, manage regulatory documents, and collaborate across functions to gain hands-on experience in the pharmaceutical sector. The ideal candidate will be a current student or recent graduate in Pharmaceutical Sciences, fluent in Portuguese and have a good command...

A leading pharmaceutical company in Porto is seeking an Administrative Assistant to support its Regulatory Affairs Department. The role involves managing regulatory files, providing administrative support, and ensuring compliance with regulatory requirements. The ideal candidate will have prior experience in a regulatory or compliance environment, strong organizational skills, and the ability to...

Administrative Assistant - Regulatory Affairs Date: Jan 13, 2026 Location: Porto Salvo, Portugal, 2740-245 Job Id: 65854 Who we are Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and...