Trabajo de Regulatory Affairs Specialist

Desde ManpowerGroupTalent Solutions estamos buscando a un/a Regulatory Affairs Specialist Europe para el para el Área de B2B de una multinacional farmacéutica referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Tu misión dentro del departamento consistirá en garantizar el cumplimiento normativo mediante la preparación y gestión eficiente de submissions regulatorias para...

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...

A global healthcare company in Sant Cugat del Vallès seeks a Regulatory Affairs Specialist Lab Automation to enhance regulatory compliance. This hybrid position requires a Bachelor's degree in a Life Sciences field and 2-5 years of regulatory experience, specifically with IVDR and FDA regulations. The role involves maintaining interfaces with regulatory authorities, creating dossiers, and...

Descripción: Seleccionem un/a Regulatory Affairs Specialist per a una empresa de referència en el sector cosmètic situada a la comarca d’Osona. Ubicació: Vic (Barcelona – Osona) Funcions principals - Aplicar la normativa i el reglament vigent relacionats amb matèries primeres, envasos i productes finals. - Gestionar el contacte amb proveïdors per obtenir la informació necessària per al...

Una empresa internacional de alimentación infantil, con sede en Cataluña, busca un Regulatory Affairs Specialist. La persona seleccionada garantizará el cumplimiento normativo en productos de alimentación infantil, supervisando el etiquetado, asesorando equipos sobre requisitos regulatorios y gestionando la documentación correspondiente. Se requieren titulación en áreas relacionadas y un nivel...

Join to apply for the Regulatory Affairs Specialist role at ESTEVE. Overview Manage the regulatory lifecycle of US FDA‑approved products, ensuring ongoing compliance and supporting regulatory activities for new product development projects. Work closely with cross‑functional teams including Global Regulatory, clinical, pharmacovigilance, and external partners to ensure timely and accurate...

Location: Barcelona City: Sant Just Desvern State: Barcelona (ES-B) Country: Spain (ES) Requisition Number: 42758 BUNGE has an exciting opportunity available for a Customs & Regulatory Affairs Specialist. In this role, you will be responsible to support Customs, Excise Duties and Trade Compliance activities across the WE Countries, ensuring that all global regulations are met, and the...

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 Submission Management - Prepare, review, and manage regulatory submissions under CTR using CTIS. - Handle regulatory submissions for medical devices, GMOs, and local country requirements in countries where CTIS...

Regulatory Affairs Specialist – Medical Devices The 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...

Regulatory Affairs Specialist (Full-time, Permanent) Prinova is a leading global supplier of ingredients and premix manufacturing solutions for the food, beverage and nutrition industries. With strategic stocks in 35+ centres around the world and manufacturing facilities in the UK, China and the USA, Prinova’s premix business is underpinned by over 40 years of experience in ingredient sourcing...

We are looking for a Senior Regulatory Affairs Specialist to join our regulatory team either in France (Eybens) or Spain (San Agustin Del Guadalix). You will be responsible for ensuring the regulatory compliance of products and services for assigned countries and maintaining alignment with authorities, customers, and internal stakeholders. You will contribute to strategic regulatory analysis,...

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 medical technology company in Barcelona is looking for a Quality & Regulatory Affairs Specialist to enhance quality and regulatory processes. This role involves preparing regulatory submissions, conducting audits, and collaborating on compliance initiatives. Candidates should have a Bachelor’s degree in a relevant field and 2 years of experience in the medical device industry. Strong...

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 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...

A leading global supplier of ingredients is seeking a Regulatory Affairs Specialist to manage compliance with food and feed regulations in Spain, the EU, and the UK. The role requires over 5 years of regulatory experience, excellent analytical skills, and the ability to monitor legislative changes impacting the business. Candidates should have strong communication skills and be proficient in...

A global healthcare company is seeking a Nucleic Acid Testing (NAT) Regulatory Affairs Specialist to join their Diagnostic Regulatory Affairs department. The candidate will prepare technical documentation, manage product registrations, and ensure compliance with regulations. Applicants should possess a Bachelor's in Health Sciences, experience in Regulatory Affairs within pharmaceuticals, and be...

Desde ManpowerGroupTalent Solutions estamos buscando a un/a Regulatory Affairs Specialist Europe para el para el Área de B2B de una multinacional farmacéutica referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Tu misión dentro del departamento consistirá en garantizar el cumplimiento normativo mediante la preparación y gestión eficiente de submissions regulatorias...

Desde Manpower Group Talent Solutions estamos buscando a un/a Regulatory Affairs Specialist Europe para el para el Área de B2 B de una multinacional farmacéutica referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Tu misión dentro del departamento consistirá en garantizar el cumplimiento normativo mediante la preparación y gestión eficiente de submissions regulatorias...

Desde ManpowerGroupTalent Solutions estamos buscando a un/a Regulatory Affairs Specialist Europe para el para el Área de B2B de una multinacional farmacéutica referente en medicamentos genéricos de valor añadido, ubicada en Martorelles. Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado para esta oportunidad? Tu...