R&D, Pharmacovigilance & Regulatory Affairs_tr

Ar-Ge, Farmakovijilans ve Ruhsatlandırma İşleri

Yeni ilaç çözümleri araştırma, geliştirme, test etme ve piyasaya sürme. Geliştirme süreci 8 ila 10 yıl sürer ve 4 fazdan oluşur.

  • Ar-Ge, Farmakovijilans ve Ruhsatlandırma İşleri

    Yeni ilaç çözümleri araştırma, geliştirme, test etme ve piyasaya sürme. Geliştirme süreci 8 ila 10 yıl sürer ve 4 fazdan oluşur.
Başlık Konum Tarih Sort descending Req ID
Sıfırla
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 27 Şub 2026 5993
PARMA, IT 27 Şub 2026 5993
Sr. Manager, CMC Regulatory Affairs
Sr. Manager, CMC Regulatory Affairs United States, US 20 Şub 2026 6204
United States, US 20 Şub 2026 6204
Clinical Program Leader, Neonatology & Care
Clinical Program Leader, Neonatology & Care Europe, IT 19 Şub 2026 6955
Europe, IT 19 Şub 2026 6955
R&D Manufacturing & Technology Transfer Manager
R&D Manufacturing & Technology Transfer Manager Parma, IT 18 Şub 2026 6501
Parma, IT 18 Şub 2026 6501
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 16 Şub 2026 6111
Europe, IT 16 Şub 2026 6111
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026
Intern, Regulatory Affairs, Global Rare Diseases - Summer 2026 Cary, NC, US 14 Şub 2026 6413
Cary, NC, US 14 Şub 2026 6413
Senior Director, Clinical Biometrics & Analytics
Senior Director, Clinical Biometrics & Analytics Parma, IT 12 Şub 2026 6387
Parma, IT 12 Şub 2026 6387
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Europe, IT 10 Şub 2026 6592
Europe, IT 10 Şub 2026 6592
Pharmazeut (all genders) im Praktikum für 2026 / 2027
Pharmazeut (all genders) im Praktikum für 2026 / 2027 Hamburg, DE 6 Şub 2026 351
Hamburg, DE 6 Şub 2026 351