01.06.24 | Vollzeit | Maintal | NORMA Group Holding GmbHGood to great! Product 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
Später ansehen30.05.24 | Vollzeit | Nordwalde | www.actief-personal.deSpecializing in human resources or commercial training and further training as a human resources manager (m/f/d) or comparable qualification - Several years of professional experience in operational HR work - Experienced in using HR software; preferably SAP - Very good knowledge of MS Office - Independent
Später ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen22.05.24 | 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 ansehen22.05.24 | 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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