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
Head of Biologic Drug Substance - Process & Analytical Development Parma, IT 29 May 2026 7233
Global Pharmacovigilance Medical Safety Writer - Temporary Parma, IT 27 May 2026 7237
INTERN - Patient Engagement
INTERN - Patient Engagement PARMA, IT 25 May 2026 5993
PARMA, IT 25 May 2026 5993
TESISTA - Digitalizzazione dei processi di laboratorio Parma, IT 20 May 2026 7305
R&D Data Visualization Engineer
R&D Data Visualization Engineer Parma, IT 19 May 2026 7301
Parma, IT 19 May 2026 7301
Translational and Precision Medicine Lead 1
Translational and Precision Medicine Lead 1 Europe - remote, GB 15 May 2026 7208
Europe - remote, GB 15 May 2026 7208
Senior Director, Clinical Excellence AIR - Bronchiectasis & Non-obstructive Lung Diseases Europe, IT 14 May 2026 6111
INTERN - Clinical Supply Management & Distribution Parma, IT 13 May 2026 7186
R&D Bioinformatician Lead
R&D Bioinformatician Lead Parma, IT 13 May 2026 7280
Parma, IT 13 May 2026 7280
Master's thesis in computational modelling of aerosol deposition in respiratory system Parma, IT 10 May 2026 6598
Senior Director, Clinical Biometrics & Analytics Parma, IT 10 May 2026 6387
Senior Manager, CMC Regulatory Affairs, Global Rare Diseases Europe, IT 8 May 2026 6592
Pharmaceutical Affairs Manager | All genders | Full-time Vienna, AT 5 May 2026 7255
Pharmazeut (all genders) im Praktikum für 2027 Hamburg, DE 4 May 2026 351