PV and Regulatory Affairs Expert

About UsAt PrimeVigilance, we pride ourselves on achieving global organic growth year after year. Our dedicated staff across Europe, North America, and Asia covers services within Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance.Job RoleThe Specialist, Regulatory and PV Network will be responsible for providing strategic...

About the Role:We are seeking an experienced Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will play a critical role in maintaining company continued compliance with European regional and national chemicals legislation.The successful candidate will have a strong understanding of chemical legislation...

.Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 17 markets.We always aim to leverage cutting-edge technology, providing the best experience to our millions of customers who trust us for their entertainment.We are a diverse team of more than 2.700 Kaizeners, from 40+ nationalities spreading across...

.We are Kaizen GamingKaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 17 markets.We always aim to leverage cutting-edge technology, providing the best experience to our millions of customers who trust us for their entertainment.We are a diverse team of more than 2,700 Kaizeners, from 40+...

Company DescriptionPrimeVigilance (part of Ergomed Group) is a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America, and Asia covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs, and...

Kaizen Gaming, the team powering Betano, is one of the biggest GameTech companies in the world, operating in 17 markets.We always aim to leverage cutting-edge technology, providing the best experience to our millions of customers who trust us for their entertainment.We are a diverse team of more than 2.700 Kaizeners, from 40+ nationalities spreading across 3...

Company OverviewRandstad II - Prestação de Serviços, Limitada is a chemical group with activities in several markets worldwide. Our company aims to strengthen its Regulatory Affairs Department.Job DescriptionThe team responsible for preparing and submitting biocide and medical device registration dossiers meeting requirements according to BPR and MDR...

Social network you want to login/join with:Regulatory Affairs Associate (M/F) - Lisboa, LisbonClient: Kelly ServicesLocation: Lisbon, PortugalJob Category: OtherEU work permit required: YesJob Reference: e6ad7d0634d1Job Views: 21Posted: 09.02.2025Expiry Date: 26.03.2025Job Description:As a Regulatory Affairs officer, your responsibilities will include:1....

As a Regulatory Affairs officer, your primary responsibility will be to update and maintain technical documentation for medicinal products in accordance with applicable regulatory requirements.Key Responsibilities:Update and maintain technical documentation for medicinal products;Collaborate with cross-functional teams to gather necessary documentation and...

About Amgen SAAmgen is a leading biotechnology company that employs innovative science to serve patients. We are shaping the future of healthcare by pioneering novel therapeutic approaches.We foster innovation, excellence, and inspiration within our organization. Our Lisbon office is home to a diverse community of talented individuals from various...

Our client is a chemical group, with activities in several markets worldwide, that want to strengthen their Regulatory Affairs Department. This team is responsible for preparing and submitting biocide and medical device registration dossiers meeting requirements according to BPR and MDR.responsabilidades chaveAs a member of the registration team having the...

Our client is a chemical group, with activities in several markets worldwide, that want to strengthen their Regulatory Affairs Department. This team is responsible for preparing and submitting biocide and medical device registration dossiers meeting requirements according to BPR and MDR.Responsabilidades Chave1. As a member of the registration team having...

About the CompanyIQVIA LLC is a leading global provider of clinical research services, commercial insights, and healthcare intelligence. We create connections that accelerate the development and commercialization of innovative medical treatments.Job SummaryThis is an exciting opportunity to join our team as a Pharmaceutical Compliance Expert. The successful...

.Press continue to see content specific to your location.United StatesRegulatory Affairs SpecialistLisboaEUR 30,000 - 40,000Be among the first applicants.TodayDescriptionKenvue is currently recruiting for a Regulatory Affairs Specialist.Start date: As soon as possible.Who We Are:At Kenvue, we realize the extraordinary power of everyday care.Built on over a...

The Regulatory Affairs Specialist will play a critical role in ensuring that our DORA project complies with all relevant regulations and laws. This individual will be responsible for interpreting and applying security requirements, assessing cybersecurity risks, and providing recommendations to management.Responsibilities:Regulatory Research: Conduct...

Job Description:The Regulatory Affairs Specialist will be responsible for maintaining company continued compliance with European regional and national chemicals legislation. This involves preparing and submitting registration dossiers in the framework of the Biocidal Products Regulation, supporting both national authorizations (pre-BPR) as well as obtaining...

Join Our TeamWe are seeking a highly motivated Regional Regulatory Affairs Senior Associate to join our team at Amgen Inc. (IR). As a key member of our regulatory affairs group, you will be responsible for providing European regional regulatory leadership and expertise for the development, registration, and lifecycle management of all Amgen molecules.About...

Job DescriptionYour role will involve participation in the preparation and revision of informative texts for healthcare professionals and patients in the EU and non-EU markets. You will manage the creation and maintenance of CCDS/CCSI/RSI, collaborate with relevant departments, and ensure communication to internal and external stakeholders regarding new and...

Our client is a chemical group, with activities in several markets worldwide, that want to strengthen their Regulatory Affairs Department. This team is responsible for preparing and submitting biocide and medical device registration dossiers meeting requirements according to BPR and MDR. Responsabilidades Chave As a member of the registration team having...

Company OverviewTN Portugal is a leading provider of innovative solutions in the field of regulatory affairs for medicinal products.Job DescriptionAs a Regulatory Affairs Associate at TN Portugal, you will play a key role in ensuring compliance with regulatory requirements for medicinal products.You will be responsible for updating and maintaining technical...