Qualification & Validation Specialist Location: On site - Barcelona Type: Full-time Are you the kind of person who won’t rest until every system, process, and piece of equipment runs exactly as it should — and can
Consultant Medical Information - German Location: Hybrid / Madrid Type: Full-time The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production
Quality Assurance Consultant Location: Barcelona - On-site Type: Full-time At QbD Group, we support the life sciences industry — pharma, biotech, medical devices, and digital health — across the entire product life cycle. You’ll join an award-winning,
Associate Consultant Toxicology Location: Hybrid - Madrid Type: Full-time QbD Group is a pan-European life sciences consultancy with 600+ experts across 8+ countries, helping pharmaceutical, biotech and medtech companies bring their products to patients: fast, compliance and
Location: Warsaw & Madrid/Barcelona– hybrid work Type: Full-time Join our CMC Regulatory Affairs team and work on complex projects supporting the development, registration, and lifecycle management of medicinal products. You will combine your CMC expertise with
Young Potential Program Location: Hybrid Type: Full-time QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking
HR Trainee Location: Barcelona (Hybrid) Type: Full-time QbD Group, a specialized consultancy company, partner of life sciences companies. We globally support our clients in the development, transformation and integral management of the life cycle of their products
Location: Warsaw & Madrid/Barcelona– hybrid work Type: Full-time What you’ll be doing CMC Activities Lead complex CMC projects and provide strategic advice on pharmaceutical development, manufacturing, testing, lifecycle management, and global regulatory requirements; Coordinate the preparation,
Drug Safety Trainee Location: Hybrid - Madrid Type: Full-time The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution
Quality Management Specialist At QbD Group, we support the life sciences industry — pharma, biotech, medical devices, and digital health — across the entire product life cycle. You’ll join an award-winning, fast-growing international team of 650+ experts,
Job Summary Experiencia, cualificaciones y habilidades interpersonales, ¿tiene todo lo necesario para triunfar en esta oportunidad? Descúbralo a continuación. Join QbD Group as a Validation & Qualification Engineer (SCADA experience). What’s in it for you Make a
At Ferrer we use business to fight for social justice. We have long been a company that looks to do things differently; instead of maximizing shareholder returns, we reinvest much of our profit in initiatives that
Consultant Medical Information - German Revise detenidamente toda la documentación de la solicitud antes de hacer clic en el botón de solicitar al final de esta descripción. Location: Hybrid / Madrid Type: Full-time The QbD Group supports
QbD Group is seeking an experienced Regulatory Affairs professional to join as Consultant Regulatory Affairs & Publishing. Hybrid role based in Madrid or Warsaw, leading submissions across Europe and guiding regulatory strategy for lifecycle management. Siga leyendo
QbD Group in Madrid is seeking a Trainee or Junior in Pharmacovigilance to assist in managing cases and ensuring compliance with safety regulations. ¿Interesado en saber más sobre este trabajo? Desplácese hacia abajo y descubra qué habilidades,
QbD Group is seeking a Consultant Medical Information with German language proficiency for a hybrid role in Madrid. Consulte la descripción del puesto a continuación. Si confía en que tiene las habilidades y la experiencia adecuadas, envíe
The QbD Group supports life sciences companies worldwide from idea to patient. QbD’s team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in ATMP, Biotech, Medical Devices, In
Join to apply for the Qualification & Validation Specialist role at QbD Group QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and
QbD Group team offers knowledge & tailored (software) solutions in development, clinical, regulatory & compliance, production and distribution for companies active in Pharma, ATMP and Medical Devices/IVD. We are always looking for the next QbD’er in Qualification/Validation. What
QbD Group is seeking an experienced Regulatory Affairs professional to join as Consultant Regulatory Affairs & Publishing. Desplácese hacia abajo para obtener una visión general completa de lo que requerirá este trabajo. ¿Es usted el candidato adecuado