Regulatory Affairs Consultant specializing in CMC for biological products, focusing on dossier preparation, drug development support, and project management within the pharmaceutical industry....
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization of
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization of
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Position Summary The R&D Data, Data Science and Artificial Intelligence (DDSAI) organization is seeking a hands‑on Principal Scientist, Data Science to design, build, and scale AI/ML, simulation, forecasting, optimization, decision intelligence, and digital twin capabilities that
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization of
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization of
At ITALFARMACO, we are firmly committed to contributing sustainably to the improvement of peoples health and quality of life. We are an Italian pharmaceutical group with an international presence, dedicated to the research, development, and commercialization of
Company Description We are SGS – the worlds leading testing, inspection and certification company. We are recognized as the global benchmark for sustainability, quality and integrity. Our 99,500 employees operate a network of 2,500 offices and
In a nutshell Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge
In a nutshell Position: Regulatory Affairs Manager - Biosimilars Location: Madrid (on-site) Experience: 5+ years in Regulatory Affairs within biotech/biopharma Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, bringing specialist knowledge
Role Overview: The Global Project Manager (GPM) is responsible for planning, coordinating, and tracking global biosimilars development projects from early development through regulatory submission and lifecycle management. The role ensures cross-functional alignment, timely execution, and adherence to scope,
Asphalion is growing and we are looking for a Scientific & Regulatory Affairs officer to join our team of CMC unit for the pharmaceutical industry! Someone who loves to take on new challenges, to work in an
Sales Specialist - Toxicology ¿Tiene las cualificaciones y habilidades adecuadas para este trabajo? Descúbralo a continuación y pulse en solicitar para ser considerado. Location : Hybrid Type : Full-time QbD Group is a pan-European life sciences
In a nutshell Position: Regulatory Affairs Biosimilar Specialist LATAM Location: Madrid Experience: 5+ years in Regulatory Affairs within innovative biopharmaceuticals and/or biosimilars Se pueden requerir diversas habilidades interpersonales y experiencia para el siguiente puesto. Por favor,
Role Overview: No espere a enviar su solicitud después de leer esta descripción; se espera un gran volumen de candidaturas para esta oportunidad. The Global Project Manager (GPM) is responsible for planning, coordinating, and tracking global