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Regulatory Affairs Specialist (m/f)
Eingestellt von Hays aus Mannheim, Universitätsstadt
Projektbeschreibung
REFERENZNUMMER:
353541/11
IHRE AUFGABEN:
-Prepare, coordinate and submit variation files, mainly CMC variations
-Working with Swissmedic portal
-Liaise with all relevant internal departments and partner companies to ensure availability of required documentation and to discuss the status of the variations
-Prepare and submit variations
and answer questions about submissions
IHRE QUALIFIKATIONEN:
-Bachelor, PTA, CTA, MTA or similar education
-Experience in a pharmaceutical industry, especially in the regulatory affairs area
-Good computer skills (MS Office applications esp. Word, Excel and PowerPoint)
-Fluent in English (written and oral), very good knowledge in German
-Excellent planning and organisational skills
-Team player mentality and good communication skills
WEITERE QUALIFIKATIONEN:
Regulatory affairs manager
353541/11
IHRE AUFGABEN:
-Prepare, coordinate and submit variation files, mainly CMC variations
-Working with Swissmedic portal
-Liaise with all relevant internal departments and partner companies to ensure availability of required documentation and to discuss the status of the variations
-Prepare and submit variations
and answer questions about submissions
IHRE QUALIFIKATIONEN:
-Bachelor, PTA, CTA, MTA or similar education
-Experience in a pharmaceutical industry, especially in the regulatory affairs area
-Good computer skills (MS Office applications esp. Word, Excel and PowerPoint)
-Fluent in English (written and oral), very good knowledge in German
-Excellent planning and organisational skills
-Team player mentality and good communication skills
WEITERE QUALIFIKATIONEN:
Regulatory affairs manager
Projektdetails
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
-
Kategorie:
Sonstiges