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
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,
Overview In this role you will lead analytical development activities for new chemical entities and solid dosage forms, guiding a multidisciplinary team to drive method development, validation, transfer, and regulatory-compliant delivery across preclinical to Phase III
QbD Group is seeking a Senior Consultant in Regulatory Affairs & Publishing to lead complex regulatory projects across Life Sciences while taking on a Team Leader role. Antes de solicitar este puesto, por favor, lea la siguiente
Overview In this role you will lead analytical development activities for new chemical entities and solid dosage forms, guiding a multidisciplinary team to drive method development, validation, transfer, and regulatory-compliant delivery across preclinical to Phase III
A leading life sciences company in Barcelona is seeking a Qualification and Validation Specialist to ensure quality in validation processes within the pharmaceutical and medical device industries. Asegúrese de enviar su solicitud rápidamente para maximizar sus
Your mission The Senior Analytical Development Manager will be responsible for leading and managing Analytical Development activities within the Pharmaceutical Development Department. The Senior Analytical Development Manager will be responsible for leading and managing Analytical Development
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
A life sciences consulting firm is looking for a Validation & Qualification Engineer to join their team in Spain. ¿Tiene las habilidades necesarias para este puesto? Lea todos los detalles a continuación y presente su candidatura
Join to apply for the Qualification & Validation Specialist role at QbD Group Inscríbase rápido, consulte la descripción completa desplazándose hacia abajo para conocer todos los requisitos de este puesto. QbD Group team offers knowledge & tailored (software)