Medical Affairs Director with Regulatory Expertise

Job OverviewThis is a senior-level position for a medical device assessor with expertise in regulatory affairs, seeking to join our team at Buscojobs Portugal.

Transformative Opportunity in Regulatory AffairsThis is a pivotal role at Thermo Fisher Scientific, an inclusive employer and a member of the LGBTQ+ business community. We're seeking an experienced Senior Manager to lead our Regulatory Affairs team in Europe.About the JobAs a Senior Manager of Regulatory Affairs, you will be responsible for ensuring...

Company Overview: Thermo Fisher Scientific is an inclusive employer and a member of myGwork, the largest global platform for the LGBTQ+ business community. As a leading life sciences company, we strive to make a positive impact on a global scale.Estimated Salary Range: $120,000 - $180,000 per annum, depending on experience.Job Description: We are seeking a...

Job OverviewWe are seeking a Regulatory Affairs Specialist to join our team at AbbVie. The successful candidate will be responsible for ensuring the maintenance of Marketing Authorisations and Medical Devices registrations.Key Responsibilities:Maintain Marketing Authorisations and Medical Devices registrations through variations and other regulatory...

Job OverviewWe are seeking a highly skilled Global Medical Affairs Director to join our team at Organon.

The Country Medical Director role at Organon is a key position that oversees the local medical organization. The incumbent reports into the Regional Medical Directors/Heads and is responsible for Field Medical and Medical Services teams. Responsibilities:Medical Strategy: Developing local Organon Medical strategy with a focus on supporting global Medical...

Role OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at AbbVie. This role will be responsible for maintaining Marketing Authorisations and Medical Devices registrations, ensuring compliance with local legislation and corporate requirements.About the JobThis position is focused on providing regulatory support for the...

About the RoleThe Senior Medical Director will serve as the primary country-level contact for local medical organizations, reporting directly to Regional Medical Directors/Heads. This role oversees Field Medical and Medical Services teams, ensuring seamless execution of medical strategies.ResponsibilitiesOversight of all aspects of local Medical Affairs,...

Job SummaryThe Country Medical Director plays a pivotal role in local and global medical strategy development, serving as the primary country-level contact for the local medical organization. As a key member of the Regional Medical Directors/Heads team, this position oversees Field Medical and Medical Services teams, ensuring seamless support for Company...

Job SummaryWe are seeking a highly experienced Senior Medical Strategy Director to join our team at Biom?Rieux Bv. This is an exciting opportunity to lead medical strategy and operations for the country, working closely with global teams to drive business growth.About the RoleThe Senior Medical Strategy Director will be responsible for developing and...

About Haleon PortugalHaleon, a new world-leading consumer health company, is seeking an experienced Regulatory Affairs Officer for its R&D department. As a key member of the team, you will play a crucial role in ensuring compliance with relevant laws and regulations.Key Responsibilities:Dossier Preparation and Submission: Prepare and submit dossiers to the...

**Country Medical Director Position at Biom?Rieux Bv**Biom?Rieux Bv is seeking a Country Medical Director to serve as the primary country-level contact for the local medical organization. This role reports into the Regional Medical Directors/Heads and oversees Field Medical and Medical Services teams.Key Responsibilities:Country Medical team focusing on...

About the RoleWe are currently recruiting for a Regulatory Affairs Specialist to join our team in Sintra, Portugal. This is an exciting opportunity to work with a leading pharmaceutical company and contribute to the launch of new products.Key Responsibilities:Handling post-approval activities related to Abbreviated New Drug Applications (ANDAs), Marketing...

About the RoleWe are seeking a highly experienced Lead Medical Devices Specialist - Regulatory Affairs to join our team at SGS. This is an excellent opportunity for a skilled professional to take their career to the next level and make a significant impact in the field of certification.

Job OverviewThe Country Medical Director plays a pivotal role in our global healthcare organization, serving as the primary country-level contact for local medical organizations. Reporting directly to Regional Medical Directors/Heads, this key position oversees Field Medical and Medical Services teams.Responsibilities:Oversight of all aspects of local...

About the RoleElanco, a global leader in animal health, is seeking a highly skilled Regulatory Affairs Professional to join our team. This role will play a critical part in fostering a molecule from concept through development and approval.The ideal candidate will have a deep understanding of pharmaceutical development processes, regulatory strategies, and...

Adalvo, a dynamic and fast-paced company based in Portugal, seeks an exceptional Regulatory Affairs Lifecycle Process Specialist to join its team. Job SummaryThe successful candidate will be responsible for ensuring compliance with applicable laws, regulations, and guidelines to facilitate the approval of all post-approval activities of products.About the...

Job Description:A challenging opportunity has arisen for a highly skilled Regulatory Medical Writer Lead to join Prime Vigilance Ltd, a leading global company specializing in pharmacovigilance services.Job Summary:The successful candidate will be responsible for leading a team of medical writers in the preparation of high-quality regulatory documents,...

Role OverviewWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at AbbVie. In this role, you will be responsible for ensuring the maintenance of Marketing Authorisations for medicinal products and Medical Devices registrations through variations and other regulatory submissions.About the RoleThe ideal candidate will have a life...

About the RolePharmaLex is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our labelling and regulatory submissions group, you will be responsible for managing the creation and maintenance of regulatory documentation, including SmPCs, PILs, and labelling.Key ResponsibilitiesParticipate in the preparation and revision...