Trabajo de regulatory affairs junior en Zaragoza

Quality & Regulatory Affairs Manager – Sector OTC (Barcelona)¿Todo listo para enviar su solicitud? Por favor, lea la descripción al menos una vez antes de hacer clic en "Solicitar".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...

Hace 1 día Sé de los primeros 25 solicitantes Enviar mensaje directo al anunciante de SOMVITAL En el laboratorio no solo se miden parámetros: se cuida la esencia de lo que ofrecemos. Cada certificado, cada validación, cada ficha técnica representa mucho más que un trámite: es la garantía de que nuestros productos cumplen con los más altos estándares y llegan al mercado con rigor y...

A prominent medical technology company in San Agustín del Guadalix is seeking a Regulatory Affairs Trainee to support the EMEA team with GTM activities in Spain and Portugal. Responsibilities include handling product notifications and assisting with CE mark activities and international registrations. Candidates must have a university degree in Life or Engineering Science or equivalent, and an...

A global medical technology company is seeking a Regulatory Affairs professional in San Agustín del Guadalix, Spain. The role focuses on aligning regulatory strategies with business objectives, preparing registration dossiers, and ensuring compliance with local and global regulations. Candidates should have a scientific background and 3-5 years of experience in Regulatory Affairs within the...

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,...

Somos un grupo internacional innovador, con amplia experiencia en la comercialización de productos farmacéuticos en el ámbito geográfico de Centroamérica y el Caribe. Objetivo principal del puesto: Gestionar los registros sanitarios de los diferentes productos comercializados en el territorio donde opera el Grupo ya sean medicamentos, producto cosmético, producto natural, suplemento alimenticio o...

Mediktor is looking for a QA/RA specialist! Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada. If you are passionate about applying the regulation to cutting edge technology and you would like to discover the Software Medical Device regulation, we are looking for you! The Team: As a member of the...

Position Overview ¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación.The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring...

Please note this position can be located in our offices in Barcelona with 2 days on site. Por favor, verifique que tiene el nivel de experiencia y las cualificaciones adecuadas leyendo la descripción completa de esta oportunidad a continuación. G&L Scientific is a specialist provider to the healthcare industry for all types of Regulatory Affairs and Quality Assurance consultancy work – and we are...

Medical Science Liaison – Spain Role: Full-time, permanent Location: Barcelona, SpainThe Role: As a result of the continuous growth of our company and upcoming launches of new original products, we are now looking to hire our first Medical Science Liaison within Spain.We’re seeking a driven and organised individual to act as a scientific and medical field-based expert to external and internal...

About the company OMODA Motors, part of the Chery Group, is an international automotive brand expanding in Europe. Our European headquarters is in Barcelona, leading the brand’s development across the region.Work arrangement This position is based fully on-site at our Barcelona office.Why join us? • Join one of the fastest-growing global automotive brands leading innovation in Europe.• Shape...

Job SummaryThe Product Security Manager is responsible for developing and managing a central Secure Development Lifecycle program, to ensure security and privacy by design across the entire product portfolio, covering all stages from pre-market development to post-market surveillance. This role involves developing and implementing global security strategies, conducting risk assessments,...

Quality Control (QC) Technician – Biologics - Morning Shift 6am-2pmConsulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe su solicitud hoy mismo.We are seeking a highly motivated and detail-oriented Quality Control Technician to join our team, specializing in the analysis of biological products. This role involves hands-on...

Our mission We turn data into better healthcare. With our insights, we make healthcare more affordable, and better, and we improve the patient's and clinicians' experience. Your impact and responsibilities Responsibilities - Project Management: Planning and executing study protocols co-developed by pharmaceutical companies, setting up analyses, and managing projects. This involves proactively...

SAVANA ( ) is an award-winning, international medical company aiming to accelerate health science by putting into the hands of healthcare providers the power to unlock all of the clinical value embedded within existing Electronic Health Records (EHRs) with Artificial Intelligence and Natural Language Processing. Always ensuring maximum privacy and security. ¿Tiene su CV preparado? Si es así y...

Overview Job Description Summary Being a key strategic partner for the EMEA BD Business by (i) supporting the implementation of registration/regulatory strategies for the UCC-SRG portfolios, closely aligned with the region's commercial objectives, to meet EMEA market requirements and (ii) securing local markets by maintaining local licenses compliant with changes related to local/global...

A leading global medical technology company is seeking a Regulatory Affairs Trainee in San Agustín del Guadalix, Spain. The role involves supporting GTM activities and coordinating with national authorities, along with managing product notifications and audits. Candidates should possess a university degree related to Life or Engineering Science and hold an internship agreement with their...

Descripción del trabajo Position Overview The Director of Quality and Regulatory Affairs will play a central role in defining and executing the organization's overall quality and regulatory roadmap. This position oversees the Quality Control, Quality Assurance, and Regulatory Affairs functions, ensuring that operations, systems, and products consistently meet applicable GxP and global regulatory...

Overview Job Description Summary As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. Job Description Main responsibilities include: GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customers BD, SA...

Overview As Regulatory Affairs Trainee you will develop yourself in supporting the activities of the EMEA (Europe, Middle East and Africa) Regulatory Affairs team. Main responsibilities GTM activity at the level of Iberia (Spain and Portugal); product notifications, communications with National CA, support to business, tenders and customers BD, SA manufacturer: CE mark activity, international...