23.01.20 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGAssociate Director CMC Dossier Management (m/f/d) Author and coordinate submission documentation preparation for all phases of clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities
Später ansehen23.01.20 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGAssociate Director CMC Dossier Management (m/f/d) Author and coordinate submission documentation preparation for all phases of clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities
Später ansehen25.01.20 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGPreparation for all phases of clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities during submission and agency review process, respectively. Leverage extensive biologics and small molecule drug
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24.01.20 | Vollzeit | Ludwigshafen am Rhein | RASCHIG GmbHAdditives and monomers and their application areas such as pressure sensitive adhesives, coatings, thermoplastics - Understanding of the electroplating industry/chemistry, battery manufacturing and/or pharma ingredients for API synthesis - Ability to understand competitive moves and counter them - Advanced
Später ansehen10.01.20 | Vollzeit | Ludwigshafen am Rhein | uniceptaUnd Erstellung von mittleren bis große Medienspiegeln aus allen für die Produkte relevanten Medienarten ist eine Deiner Aufgaben - Dabei spielt auch die Zusammenstellung der Presseresonanz in Medienspiegeln inkl. der digitalen Verarbeitung eine große Rolle - Du übernimmst die vollumfängliche Betreuung
Später ansehen24.01.20 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGPreparation for all phases of clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities during submission and agency review process, respectively. Leverage extensive biologics and small molecule drug
Später ansehen24.01.20 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGPreparation for all phases of clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities during submission and agency review process, respectively. Leverage extensive biologics and small molecule drug
Später ansehen18.12.19 | Vollzeit | Ludwigshafen am Rhein | AbbVieOf clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities during submission and agency review process, respectively. - Leverage extensive biologics and small molecule drug development experience
Später ansehen23.01.20 | Vollzeit | Ludwigshafen am Rhein | AbbVie Deutschland GmbH & Co. KGDocumentation preparation for all phases of clinical development, often under significant time pressure. Proactively author responses and drive team resolution activities to questions from regulatory authorities during submission and agency review process, respectively. • Leverage extensive biologics and small
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