Trabajo de Regulatory Affairs Manager en Madrid

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...

MFC-2510-344 REGULATORY AFFAIRS MANAGER MADRID Overall responsibilities - To provide regulatory advice and support to the organisation on the content of existing marketing authorisations and for products in development phase. - To provide general regulatory advice and support to other departments. - Review and approval of promotional and non-promotional material to comply with local...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job...

A well-established iGaming group is seeking an experienced Licensing and Regulatory Affairs Manager to join their fully remote team. The role involves ensuring correct licenses and regulatory approvals across multiple verticals, including online gambling and crypto assets. The ideal candidate will have 5–8 years of experience in licensing and regulation, particularly within Fintech, with a strong...

Regulatory Affairs Manager Crop Protection (f/m/d)2 days ago Be among the first 25 applicantsGet AI-powered advice on this job and more exclusive features.Join Us in Shaping the Future of Regulatory Services.Knoell is one of the leading global service providers in regulatory registration, clinical development, and product development support. As a family‑owned business, we take pride in our...

Quality & Regulatory Affairs Manager – Sector OTC (Barcelona)Desde LHH Life Sciences estamos seleccionando un/a Quality & Regulatory Affairs Manager para Multinacional líder en sector OTC, ubicada en Barcelona.Misión del puestoGarantizar el cumplimiento normativo, la calidad y la seguridad de los productos, estructurando y manteniendo el Sistema de Gestión de Calidad y asegurando la conformidad...

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional...

Job Title: Regulatory Affairs Specialist Spain Full Time Permanent Location: Spain (Madrid) About Novumgen Novumgen is a rapidly expanding, science-driven pharmaceutical company committed to delivering high-quality, accessible medicines across global markets. Our diverse portfolio spans specialty generics, complex formulations, and innovative therapeutic solutions. With a strong focus on...

Regulatory Affairs Study Start Up Specialist II (RASSU) - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS is not mandated, including ethics committee submissions. - Prepare and QC Clinical Trial Application forms (via CTIS or...

Staphyt veille au respect de l'égalité femmes/hommes : Cliquez ici pour télécharger l'index d'égalité femmes/hommes pour Staphyt France At Staphyt, our Regulatory Affairs Division helps clients navigate complex regulatory environments and successfully bring their chemical or biological substances and products to market. We support projects across Plant Protection & Nutrition, Biocides and REACh...

When our values align, there's no limit to what we can achieve. Parexel is seeking an experienced Regulatory Affairs Professional to join our dynamic team as a Senior Regulatory Affairs Consultant. This strategic position requires a proactive and agile regulatory professional able to build strategy, drive execution, and address challenges involved in gaining market approvals across international...

QbD Group offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, Biotech and Medical Devices/IVD. Our Regulatory Affairs division supports customers throughout the entire regulatory lifecycle of their products, whether they are traditional pharmaceutical products, generic medicines, vaccines,...

Regulatory Affairs Junior Officer/Trainee Regulatory Affairs Junior Officers/Trainees ensure and provide support for the appropriate registering, licensing, marketing, and legal compliance of pharmaceutical and medical products in order to control the safety and efficacy of products. A combination of scientific knowledge, legal and business issues ensures that products developed, manufactured,...

Regulatory Affairs Specialist – Medical DevicesThe Regulatory Affairs Specialist is responsible for preparing, submitting, and maintaining regulatory documentation to support global approvals of high‑risk or implantable medical devices. This role ensures compliance with U.S. FDA regulations, EU MDR 2017/745, and other international requirements, supporting product lifecycle management from...

A leading global healthcare technology company is seeking a Regulatory Affairs Specialist in Madrid, Spain. This role involves supporting regulatory activities for new and current products related to diabetes. The successful candidate will ensure compliance throughout the product lifecycle, strife for regulatory approvals, and collaborate with cross-functional teams. A Bachelor's degree in a...

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 What You’ll Do - Prepare, review, and manage regulatory submissions under CTR (Clinical Trials Regulation) using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in...

BettingJobs is working with a well established multi‑vertical iGaming group seeking to expand their fully remote team with an experienced Licensing and Regulatory Affairs Manager.This role has a strong reference for those based in Cyprus.This role is critical in ensuring our group of companies operates with the correct licences and regulatory approvals across multiple verticals, including online...

A leading global consultancy is seeking a Plant Protection Regulatory Affairs Project Manager in Madrid, Spain. This role involves developing regulatory strategies and managing the regulatory process for agrochemicals. Candidates should have a degree in chemistry or a related field and strong knowledge of EU regulations, alongside experience in dossier preparation. The company emphasizes...

Regulatory Affairs Specialist page is loaded## Regulatory Affairs Specialistlocations: Madrid, Madrid, Spaintime type: Full timeposted on: Posted Todaytime left to apply: End Date: January 28, 2026 (6 days left to apply)job requisition id: R55896At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead...

JOB DESCRIPTION: Responsible for supporting global regulatory submissions and maintaining compliance with regulatory requirements for pharmaceutical products across multiple regions aligned with global regulatory strategies. This role involves preparing regulatory dossiers, coordinating with health authorities, ensuring product registration, and providing regulatory guidance to cross-functional...