Trabajo de Regulatory Affairs Trainee en Madrid

Da el primer paso hacia tu futuro profesional en Laboratorios Ordesa: tu talento suma, nuestra pasión por la salud nos une.¿Todavía no sabes quiénes somos? Déjanos presentarnos…Laboratorios Ordesa es una compañía referente en el sector de la nutrición especializada, con una sólida trayectoria y en pleno crecimiento. Apostamos por la innovación, el rigor científico y el compromiso con la salud a...

𝐒𝐨𝐥𝐯𝐢𝐧𝐠 𝐜𝐡𝐚𝐥𝐥𝐞𝐧𝐠𝐞𝐬 𝐟𝐨𝐫 𝐚 𝐛𝐞𝐭𝐭𝐞𝐫 𝐟𝐮𝐭𝐮𝐫𝐞 Somos un grupo de empresas de impacto con una misión: resolver retos sociales y ambientales para un futuro mejor. Y para lograrlo, desarrollamos nuestra actividad poniendo foco en 4 líneas de negocio: Zubi Labs (Venture Builder), Zubi Capital (gestión de inversiones), Zubi Cities (innovación y desarrollo de ciudades sostenibles) e Imagine Montessori School...

CONTRATO FORMATIVO PARA LA OBTENCIÓN DE LA PRÁCTICA PROFESIONALREQUISITOS:HABER FINALIZADO ESTUDIOS EN LOS ÚLTIMOS 3 AÑOSNO HABER TENIDO UN CONTRATO DEL MISMO TIPO CON ANTERIORIDADWho we are?Veterinary medicine manufacturersVetpharma is the veterinary division of Chemo, part of the Insud Pharma group, providing Animal Health solutions. We are located in Barcelona, where the group was founded in...

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,...

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...

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...

A career at Lombard Odier means working for a renowned global wealth and asset manager, with a strong focus on sustainable investing. An innovative bank of choice for private and institutional clients, our independently owned Firm is one of the best-capitalised banking groups in the world, managing close to CHF 300 billion and operating from over 25 offices across 4 continents. With a history...

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...

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...

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. A Day in the Life Take on a pivotal role as a Regulatory Affairs Specialist in Spain, supporting both pre‑market and post‑market regulatory activities...

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...

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,...

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...

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...

When our values align, there's no limit to what we can achieve. Are you an experienced regulatory affairs professional looking for a new opportunity? We are currently seeking a talented Regulatory Affairs Consultant to join our dynamic team! This is a client dedicated project, and the role can be office or home based in various European locations. As the Regulatory Affairs Consultant you will...

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...

A global healthcare technology leader is seeking a Regulatory Affairs Specialist in Madrid, Spain. This role involves supporting regulatory activities for diabetes products, ensuring compliance throughout the product lifecycle. Candidates should have a relevant degree and 2-4 years of experience in medical device regulations specific to the Spanish market. Proficiency in Spanish and English is...