353 English-speaking jobs in Canton of Aargau

Senior QA Validation Specialist will oversee raw material quality processes, including review and approval of documentation. Responsibilities include supporting QC/QA activities, driving qualification and validation activities, and contributing to warehouse and logistics quality oversight. Requires solid QA experience in a GMP environment and fluency in English. German language skills are an advantage.

Lead GMP Quality Assurance Analyst will oversee raw material quality processes, including review and approval of documentation. Support QC and QA activities, drive qualification and validation activities, and contribute to Warehouse and Logistics quality oversight.

Leads complex end-to-end drug product transfers from development through commercial launch. Serves as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provides technical authority and acts as senior escalation point for complex technical challenges.

Lead complex end-to-end drug product transfers from development through commercial launch. Serve as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provide technical authority and act as senior escalation point for complex technical challenges. Lead process setup, scale-up, and implementation activities at GMP drug product manufacturing sites. Drive GMP change management strategy and initiate and manage GMP change control. Ensure all activities are performed according to current standards (Good Manufacturing Practice, Health Safety Environment, Regulatory etc.).

Senior Technology Transfer Lead will manage and guide complex drug product commercial transfers from New Product Introduction to commercial launch. The role requires expertise in biotech/pharma/CDMO, drug product development, and technology transfer. Responsibilities include process setup, scale-up, GMP change management, and serving as the primary technical point of contact for technology transfer.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Leads complex end-to-end drug product transfers from development through commercial launch. Serves as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provides technical authority and acts as senior escalation point for complex technical challenges.

Lead complex end-to-end drug product transfers from development through commercial launch. Serve as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provide technical authority and act as senior escalation point for complex technical challenges. Lead process setup, scale-up, and implementation activities at GMP drug product manufacturing sites. Drive GMP change management strategy and initiate and manage GMP change control. Ensure all activities are performed according to current standards (Good Manufacturing Practice, Health Safety Environment, Regulatory etc.).

Leads and guides complex drug product commercial transfers from development through launch, serving as the primary technical contact and ensuring compliance with global standards.

Coordinate raw material quality processes, including review and approval of documentation. Support QC and QA activities, drive qualification and validation, and contribute to warehouse and logistics quality oversight.

Senior QA Expert to oversee raw material quality processes, including review and approval of documentation, support QC/QA activities, and drive qualification and validation activities.

Leads complex end-to-end drug product transfers from development through commercial launch. Serves as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provides technical authority and acts as senior escalation point for complex technical challenges.

Leads and guides complex drug product commercial transfers from development through launch, serving as the primary technical contact and ensuring compliance with global standards.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Senior Technology Transfer Lead will manage and guide complex drug product commercial transfers from New Product Introduction to commercial launch. The role requires expertise in biotech/pharma/CDMO, drug product development, and technology transfer. Responsibilities include process setup, scale-up, GMP change management, and serving as the primary technical point of contact for technology transfer.

Lead complex end-to-end drug product transfers from development through commercial launch. Serve as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provide technical authority and act as senior escalation point for complex technical challenges. Lead process setup, scale-up, and implementation activities at GMP drug product manufacturing sites. Drive GMP change management strategy and initiate and manage GMP change control. Ensure all activities are performed according to current standards (Good Manufacturing Practice, Health Safety Environment, Regulatory etc.).

Leads complex end-to-end drug product transfers from development through commercial launch. Serves as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provides technical authority and acts as senior escalation point for complex technical challenges.

Leads and guides complex drug product transfers from development through commercial launch, serving as the primary technical contact and ensuring compliance with global standards.

Senior Technology Transfer Lead will manage and guide complex drug product commercial transfers from New Product Introduction to commercial launch. The role requires expertise in biotech/pharma/CDMO, drug product development, and technology transfer. Responsibilities include process setup, scale-up, GMP change management, and serving as the primary technical point of contact for technology transfer.

Lead complex end-to-end drug product transfers from development through commercial launch. Serve as global Subject Matter Expert for Process Technology Transfer, shaping technical strategy and ensuring global standard alignment. Provide technical authority and act as senior escalation point for complex technical challenges. Lead process setup, scale-up, and implementation activities at GMP drug product manufacturing sites. Drive GMP change management strategy and initiate and manage GMP change control. Ensure all activities are performed according to current standards (Good Manufacturing Practice, Health Safety Environment, Regulatory etc.).