Stellenangebot
Lead and drive formulation development and manufacturing activities for assigned projects, ensuring scientific and technological excellence focus on parenteral drug productsCollaborate closely with cr
Stellenangebot
Responsible for the design, plan, perform, interpret and report results of formulation and process development for liquid and lyophilized parenteral drug products of small molecules, biologics (e.g. o
Stellenangebot
Performing all warehouse and distribution activities in compliance with requirements and the corresponding procedures.
Performs cleaning of workplace
Performs GMP compliant documentation of the execut
Stellenangebot
Support and drive implementation of Annex 1 requirements during implementation in the Clinical Supply Centre for sterile Drug Product (Parenterals) within IMP SwitzerlandResponsible to represent Quali
Stellenangebot
...CSV), Analytics, infrastructure, critical utilities (WFI, PW, Gas) and processes within TR&D in BaselSupport of implementation of DI requirementsReview and approval of GMP relevant Documents
Basel Stadt Vollzeit
Stellenangebot
Deliver robust market and revenue model projections through extensive data analysis and collaboration on a global levelTranslate data into trends with strategic importance and business impactLead and