...operations team. With recent regulatory clearance and ambitious growth plans, they are rolling out transformative technology across Europe and the US. To support this expansion and ensure seamless pro...
...manufacturing facility is a world-class site for the production of inhaled devices. Here, there are about 450 people, producing dry powder and aerosol drugs in the field of respiratory diseases for pa...
...Manufacturing, SAP MII, SAP ME) for pharmaceutical manufacturing operations. Collaborate with cross-functional teams including Production, Quality, IT, Engineering, and Supply Chain. Integrate MES wit...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.Drafting/reviewing relevant device sections of eCTD modules (e.g. 3.2.R, ...
...Manufacturing, SAP MII, SAP ME) for pharmaceutical manufacturing operations. Collaborate with cross-functional teams including Production, Quality, IT, Engineering, and Supply Chain. Integrate MES wit...
...Manufacturing, SAP MII, SAP ME) for pharmaceutical manufacturing operations. Collaborate with cross-functional teams including Production, Quality, IT, Engineering, and Supply Chain. Integrate MES wit...