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Formulation Project Leader (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Design, Support
Projektbeschreibung
REFERENZNUMMER:
357193/1
IHRE AUFGABEN:
-Design, plan, perform, interpret and report results of scientific formulation experiments for the preparation and timely delivery of oral drug products incl. GMP manufacturing
-Lead and manage all formulation activities, support & coach team members, participate in scientific teams and contribute to the overall Technical Research and Development strategies and goals
-Key role in the development of oral dosage forms and the transfer to production
-Insure that high quality products are developed applying state of the art technologies, risk analysis and QbD methodologies
-Achieve robust formulations and processes through optimization, scale-up and validation work and provision of the required documentation to allow worldwide registration
-Representing Pharmaceutical Development in external collaborations
IHRE QUALIFIKATIONEN:
-Master or PhD with focus on pharmaceutical sciences and technology (e.g. Pharmacy, Chemistry)
-Profound industry experience in the successful development of pharmaceutical formulations (ideally oral dosage forms, solid understanding of QbD and bio pharmaceuticals)
-Excellent knowledge of laboratory and/or technical tools (e.g. QbD, statistical software, PAT)
-Broad and profound understanding of development activities and processes in pharmaceutical sciences
-Strong knowledge of relevant GLP, GMP regulations and policies
-Successfully demonstrated track record of creativity and problem solving in projects
-Fluency in English, German and/or French desired
WEITERE QUALIFIKATIONEN:
Clinical project manager
357193/1
IHRE AUFGABEN:
-Design, plan, perform, interpret and report results of scientific formulation experiments for the preparation and timely delivery of oral drug products incl. GMP manufacturing
-Lead and manage all formulation activities, support & coach team members, participate in scientific teams and contribute to the overall Technical Research and Development strategies and goals
-Key role in the development of oral dosage forms and the transfer to production
-Insure that high quality products are developed applying state of the art technologies, risk analysis and QbD methodologies
-Achieve robust formulations and processes through optimization, scale-up and validation work and provision of the required documentation to allow worldwide registration
-Representing Pharmaceutical Development in external collaborations
IHRE QUALIFIKATIONEN:
-Master or PhD with focus on pharmaceutical sciences and technology (e.g. Pharmacy, Chemistry)
-Profound industry experience in the successful development of pharmaceutical formulations (ideally oral dosage forms, solid understanding of QbD and bio pharmaceuticals)
-Excellent knowledge of laboratory and/or technical tools (e.g. QbD, statistical software, PAT)
-Broad and profound understanding of development activities and processes in pharmaceutical sciences
-Strong knowledge of relevant GLP, GMP regulations and policies
-Successfully demonstrated track record of creativity and problem solving in projects
-Fluency in English, German and/or French desired
WEITERE QUALIFIKATIONEN:
Clinical project manager
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Sonstiges