Regulatory Affairs Professional for Global Product Registration

**Company Overview**Sinclair is a global medical aesthetics organisation founded in 1971, delivering an extensive product range worldwide. With an in-house commercial infrastructure and a network of distributors, our products are sold in 55 countries.**Job Summary**We are seeking a highly skilled Regulatory Affairs Specialist to manage global product...

About the Job: We are looking for a Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices (EBD). In this role, you will ensure compliance with international regulatory authorities and support market entry for EBDs worldwide.Key Responsibilities:Manage complex projects and deliverables...

Job Description:">The Regulatory Affairs Strategist is responsible for delivering innovative global regulatory strategies for clinical trial registration with health authorities. This role oversees the regulatory aspects related to clinical trial submissions, aligning with the company's global business strategy and partnering with subject matter experts...

Company OverviewGrifols is a global healthcare company that has been working to improve the health and well-being of people around the world since 1909. We are leaders in plasma-derived medicines and transfusion medicine, developing, producing, and marketing innovative medicines, solutions, and services in more than 110 countries and regions.Job...

About the RoleWe are seeking a talented Regulatory Affairs Specialist to join our R&D team in Barcelona. As a key member of our team, you will be responsible for preparing documentation, maintaining product information files (PIFs), and managing technical dossiers for product registration in European markets.Key ResponsibilitiesPrepare and maintain PIFs and...

Job Title:Regulatory Affairs SpecialistGalderma Pharma S.A is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong...

About The Zonal Group: As a global medical aesthetics organisation, we deliver an extensive product range with an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets. Our products are sold in 55 countries worldwide.Job Description: We are seeking a Regulatory Affairs Specialist to manage the...

Job Title: Regulatory Affairs Specialist - Energy-Based DevicesAbout the Role:At The Zonal Group, we are seeking a highly skilled Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices (EBD).Key Responsibilities:Ensure compliance with international regulatory authorities and support...

Galderma Pharma S.A. is a dermatology category leader with a unique legacy and decades of innovation, present in approximately 90 countries worldwide. Our science-based portfolio spans the full spectrum of the fast-growing dermatology market through Injectables, Dermo-cosmetics, and Therapeutic Dermatology. We are seeking a highly motivated and...

Regulatory Affairs Specialist Job DescriptionSinclair EBD is seeking a skilled Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices. As a key member of our team, you will ensure compliance with international regulatory authorities and support market entry for EBDs worldwide.About...

Job Summary:At Vetpharma, we are seeking a highly skilled Regulatory Affairs Associate to join our team. The successful candidate will be responsible for compiling and managing registration dossiers and coordinating submissions to health authorities until product approval and launch.Key Responsibilities:• Compile and manage registration dossiers and...

We are advancing dermatology for every skin story by delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The Regulatory Affairs Strategist is responsible for regulatory aspects related to clinical trial regulatory submissions in alignment with the global business strategy and in partnership...

Job Title: Regulatory Affairs Specialist - EBDJob Summary:Sinclair EBD is seeking a highly skilled Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices (EBD). As a key member of our team, you will ensure compliance with international regulatory authorities and support market entry for...

The Regulatory Affairs department at Werfen is seeking a highly skilled Quality and Regulatory Affairs specialist to join our team in Barcelona, Spain.As a Quality and Regulatory Affairs specialist, you will be responsible for supporting the execution of pre and post-market regulatory affairs departmental functions. This includes assisting in the preparation...

About Solutia Life SciencesSolutia Life Sciences is a recruitment division of Solutia, specializing in technical and middle management profiles in the pharmaceutical, biotech, and medical device sectors.We are currently selecting a Regulatory Affairs Technician for a pharmaceutical company focused on developing and producing innovative oncology products and...

OverviewWerfen is seeking a Regulatory Affairs Specialist to support the execution of pre- and post-market regulatory affairs departmental functions. The ideal candidate will assist in the preparation of documentation and information required to place and keep products on the market, including regulatory submissions, licensing and registrations. Key...

About the RoleWe are seeking a highly skilled Regulatory Affairs Specialist to join our Health Sciences service line as a Project Manager in Biocides. This role will involve working with international teams to support global organizations in bringing safe, health, and environment-friendly products to the market.Your Key ResponsibilitiesLeading on projects...

Job Summary:As a Regulatory Affairs Associate at Vetpharma, you will play a crucial role in ensuring the compliance of our pharmaceutical products with regulatory requirements. Your primary responsibility will be to compile and manage registration dossiers and variation packages, coordinating submissions and follow-ups until product approval and launch.Key...

Job Title: Regulatory Affairs Specialist - EBDJob Summary: We are seeking a highly skilled Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our Energy-Based Devices (EBD).Key Responsibilities:* Ensure compliance with international regulatory authorities* Support market entry for EBDs worldwide* Collaborate...

Job Title: Manager Regulatory Affairs APIAt Sandoz, quality is a key factor embedded in our purpose of pioneering access for patients.This role provides timely preparation of high-quality CMC regulatory documentation for active ingredients/intermediates under responsibility, formulating and leading global regulatory strategy for drug substances under minor...