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Analytical Expert (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Gesuchte Skills: Design
Projektbeschreibung
REFERENZNUMMER:
342174/11
IHRE AUFGABEN:
-Design, plan, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP)
-Write analytical documents (e.g. Analytical methods, Validation reports, Stability reports)
-Responsible for analytical method development, validation, stability and release testing and transfer activities of drug substance and formulated drug product
-Contribute to the overall analytical project strategy
-Ensure GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with regulations
-Author and reviewer of GMP relevant documents (e.g. analytical methods, raw data, SOPs, qualification reports for analytical instruments, etc.)
-Review analytical batch records according to SOPs
-Identify scientific, technological and GMP issues and proposes solutions to relevant persons in the analytical project team
IHRE QUALIFIKATIONEN:
-PhD or Master in analytical chemistry or equivalent
-Profound experience in the pharmaceutical industry, preferably in analytical development
-Strong scientific knowledge in analytical development
-Fluency in English (oral and in writing)
-Desirable: GMP knowledge (work history in cGMP environment)
WEITERE QUALIFIKATIONEN:
R&D scientist
342174/11
IHRE AUFGABEN:
-Design, plan, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS) and drug products (DP)
-Write analytical documents (e.g. Analytical methods, Validation reports, Stability reports)
-Responsible for analytical method development, validation, stability and release testing and transfer activities of drug substance and formulated drug product
-Contribute to the overall analytical project strategy
-Ensure GMP compliance for all GMP relevant analytical activities of assigned projects in alignment with regulations
-Author and reviewer of GMP relevant documents (e.g. analytical methods, raw data, SOPs, qualification reports for analytical instruments, etc.)
-Review analytical batch records according to SOPs
-Identify scientific, technological and GMP issues and proposes solutions to relevant persons in the analytical project team
IHRE QUALIFIKATIONEN:
-PhD or Master in analytical chemistry or equivalent
-Profound experience in the pharmaceutical industry, preferably in analytical development
-Strong scientific knowledge in analytical development
-Fluency in English (oral and in writing)
-Desirable: GMP knowledge (work history in cGMP environment)
WEITERE QUALIFIKATIONEN:
R&D scientist
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design