29.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAs well as downtime planning Subject Matter Expert* for development, implementation and improvement of several software tools used for producution planning Forecasting and support for material sourcing activities of selected special materials and potential stock out candidates Successfully completed
Später ansehen29.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAs well as downtime planning Subject Matter Expert* for development, implementation and improvement of several software tools used for producution planning Forecasting and support for material sourcing activities of selected special materials and potential stock out candidates Successfully completed
Später ansehen29.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAs well as downtime planning Subject Matter Expert* for development, implementation and improvement of several software tools used for producution planning Forecasting and support for material sourcing activities of selected special materials and potential stock out candidates Successfully completed
Später ansehen29.04.24 | Vollzeit | Kaiserslautern | BioNTech SEAs well as downtime planning Subject Matter Expert* for development, implementation and improvement of several software tools used for producution planning Forecasting and support for material sourcing activities of selected special materials and potential stock out candidates Successfully completed
Später ansehen08.05.24 | Vollzeit | Maintal | NORMA Group Holding GmbHProduct Design Engineer (m/f/d) Responsibilities Designs NORMA Group drawings (e.g. quotation and manufacturing), the creation and tracking of part numbers, the product verification and validation process Establishes the D-FMEA (Software Apis) Defines customer-owned interfacing components (e.g
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
Später ansehen09.04.24 | Vollzeit | Kaiserslautern | BioNTech SEOn regulatory submissions, including developing ISE/ISS packages Excellent knowledge and experience of clinical development, study designs, advanced statistical methods (adaptive design and/or Bayesian is a plus), regulatory guidelines (ICH, FDA, EMA) Excellent knowledge of statistical analysis software (SAS
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