Gloor&lang AG

Sterile Manufacturing French-Speaking GMP PharmaOn behalf of our client a well-established and steadily growing pharmaceutical company with a strong reputation in sterile manufacturing and clinical supply we are seeking an experienced Deputy Qualified Person (QP) to strengthen the

Sterile Manufacturing French-Speaking GMP PharmaOn behalf of our client a well-established and steadily growing pharmaceutical company with a strong reputation in sterile manufacturing and clinical supply we are seeking an experienced Deputy Qualified Person (QP) to strengthen the

Shape Agile Pharma Drive Compliance Innovation and Continuous ImprovementAre you an experienced QMS specialist seeking a high-impact consulting assignment in the pharmaceutical industry Join us as a Global GxP Quality System Manager and help transform our agile Quality Management Sys

Shape Agile Pharma Drive Compliance Innovation and Continuous ImprovementAre you an experienced QMS specialist seeking a high-impact consulting assignment in the pharmaceutical industry Join us as a Global GxP Quality System Manager and help transform our agile Quality Management Sys

Basel HybridThis is not a routine role. We are looking for a high-impact Translational Science Leader who can step in and immediately drive critical oncology programs forward.This opportunity sits at the heart of cutting-edge R&D where science meets strategyand where your decisions w

Basel HybridThis is not a routine role. We are looking for a high-impact Translational Science Leader who can step in and immediately drive critical oncology programs forward.This opportunity sits at the heart of cutting-edge R&D where science meets strategyand where your decisions w

Shape CMC regulatory strategy for complex biologics in a fast-growing biotech environmentFor a fast-growing internationally active biotech company focused on biosimilar development we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Re

Shape CMC regulatory strategy for complex biologics in a fast-growing biotech environmentFor a fast-growing internationally active biotech company focused on biosimilar development we are currently looking for a Senior Expert Regulatory Affairs with a strong CMC focus. Workplace is Re

Region Zug Zürich HybridFor a growing biopharmaceutical development organization in the ZugZurich region we are looking for a Clinical Quality Assurance Specialist / Expert to support the quality oversight of clinical development programs.This role is suited for early to mid-career

Region Zug Zürich HybridFor a growing biopharmaceutical development organization in the ZugZurich region we are looking for a Clinical Quality Assurance Specialist / Expert to support the quality oversight of clinical development programs.This role is suited for early to mid-career

FATSAT-Projects - GMP - Oral Solid DosageYou dont just execute projects you drive them.You understand GMP OSD manufacturing and complex validation environments.And youre ready to take ownership of a critical tableting area revamp.This is your opportunity to step into a Manager / Engi

FATSAT-Projects - GMP - Oral Solid DosageYou dont just execute projects you drive them.You understand GMP OSD manufacturing and complex validation environments.And youre ready to take ownership of a critical tableting area revamp.This is your opportunity to step into a Manager / Engi

External Manufacturing GMP Oversight & CMO ManagementAre you an experienced Quality Operations professional (m/f/d) looking to take ownership in a global external manufacturing environment Our client is seeking a motivated Quality Operations Manager to provide quality oversight of Co

External Manufacturing GMP Oversight & CMO ManagementAre you an experienced Quality Operations professional (m/f/d) looking to take ownership in a global external manufacturing environment Our client is seeking a motivated Quality Operations Manager to provide quality oversight of Co

Manufacturing site - GMP documentationAre you a motivated Junior Validation Associate (m/f/d) eager to grow in a dynamic GMP-regulated environment and extend your first hands-on experience in validation activities within pharmaceutical manufacturing environment Our client seeks your m

Manufacturing site - GMP documentationAre you a motivated Junior Validation Associate (m/f/d) eager to grow in a dynamic GMP-regulated environment and extend your first hands-on experience in validation activities within pharmaceutical manufacturing environment Our client seeks your m