Trabajo de Regulatory en León

Join to apply for the Regulatory Compliance Manager role at Ebury. Regulatory Compliance Manager Overview Ebury is a global fintech firm dedicated to empowering businesses to expand internationally through tailored and forward‑thinking financial solutions. Since our founding in 2009, we’ve grown to a diverse team of over 1,700 professionals across 40+ offices and 29+ markets worldwide. Joining...

Técnico de registros /Regulatory affair specialist Técnico de registros /Regulatory affair specialist Desde Antal International estamos buscando un regulatory affair technician para una empresa dermocosmética internacional para unirse a su equipo global y colaborar estrechamente con las áreas de I+D (preclínica y clínica) en el desarrollo, revisión y lanzamiento de productos dermatológicos...

IMPORTANT – REQUIRED EXPERIENCE Experience in the pest control sector (control de plagas) or in a comparable operational service business is mandatory for this role.IMPORTANTE – EXPERIENCIA OBLIGATORIALa experiencia previa en el sector de control de plagas o en un negocio de servicios operativos comparable es obligatoria para este puesto.Si no dispone de esta experiencia, le rogamos no...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis.The Regulatory Submissions Specialist contributes to the management and development of procedures related to the activities in which he/she is involved in and ensures that the outputs of their activities meet the quality...

Buscamos un/a Regulatory Affairs para una empresa industrial de la zona de Sant Cugat. Si tienes experiencia en regulación de biocidas, cosméticos y dispositivos médicos , y buscas un nuevo reto en un entorno dinámico, ¡Queremos conocerte! Responsabilidades: Seguimiento de cambios normativos y evaluación de impacto en productos y procesos. Gestión de expedientes de registro y coordinación de...

Health in Code es una empresa líder en diagnóstico genético, comprometida con mejorar la calidad de vida de las personas a través de la medicina personalizada y la toma de decisiones clínicas basadas en datos genómicos. ¿Te interesa el ámbito de Regulatory Affairs y quieres formarte en el ciclo de vida del producto sanitario de diagnóstico genético dentro de un entorno altamente...

Axalta has remained at the forefront of the coatings industry by continually investing in innovative solutions. We engineer technologies that protect customers' products – whether they are battling heat, light, corrosion, abrasion, moisture, or chemicals – and add dimension and beauty with colourful finishes. We have a vast and ever-evolving portfolio of brands primed to play an important part in...

Asphalion is growing and we are looking for a Regulatory Affairs Senior Officer to join our CMC unit of consultants for the pharmaceutical industry ! Someone who loves to take on new challenges, to work in an international environment and who wants to grow with us! Main responsibilities: Global CMC writing/management of product specific dossiers (Mod. 2/Mod. 3), with special focus on biologics...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, Spain ....

In a few wordsPosition: QA Techinician.Location: León.Experience: Between 1-3 years.Want to know more?INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (API), finished dosage forms (FDF), and branded...

Job Description: Coordinates the preparation and submission of required monthly data reports, quarterly staff training logs, and quarterly community training logs to ensure compliance with contract requirements. Reviews community therapist monthly workbooks and billing for completeness and accuracy. Submits approved documentation to the Finance group for VOCA invoicing, ensuring adherence to...

At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Supply Planner & External Manufacturing Specialist for our Manufacturing Site in León (Spain). GLOBAL RESPONSIBILITY The Supply Planner & External Manufacturing Specialist is responsible for managing production of pharmaceutical products performed in external vendors (CMOs). Its...

Global Responsibility At mAbxience, a company specialized in the development and manufacturing of biosimilar medicines, we are hiring a Supply Planner & External Manufacturing Specialist for our Manufacturing Site in León (Spain). The Supply Planner & External Manufacturing Specialist is responsible for managing production of pharmaceutical products performed in external vendors (CMOs). Its main...

A leading fintech company is seeking a Regulatory Compliance Manager to drive regulatory initiatives and ensure compliance within a fast-paced environment. This key leadership role involves providing expert advice on licensing and product compliance, managing compliance monitoring, and leading a team of Compliance Analysts. A strong background in regulatory knowledge and analytical skills is...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, Spain . Lead and execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. We are looking for someone who can autonomously carry on the work within the scope of their activities and interacts with the Direct Manager to define priorities and manages workload. The Regulatory Submissions Specialist...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, Spain . Lead and execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute...

Ebury is a global fintech firm dedicated to empowering businesses to expand internationally through tailored and forward-thinking financial solutions. Since our founding in , we've grown to a diverse team of over 1, professionals across 40+ offices and 29+ markets worldwide. Joining Ebury means becoming part of a collaborative and innovative environment where your contributions are valued. You'll...

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, Spain . Lead and execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems . Prepare, review, and execute...

Ebury is a global fintech firm dedicated to empowering businesses to expand internationally through tailored and forward-thinking financial solutions. Since our founding in , we’ve grown to a diverse team of over 1, professionals across 40+ offices and 29+ markets worldwide. Joining Ebury means becoming part of a collaborative and innovative environment where your contributions are valued. You’ll...