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| Job Title Sort ascending | Business | Location | Site | Date Posted |
|---|---|---|---|---|
| Principal Clinical Data Scientist Regular, Full time | Development | Ireland | Dublin (NOCC) | Jul 23, 2025 |
| Global GCP/PV Auditor Regular, Full time | Other | Spain +Alternative Locations | Barcelona Provincial | Jul 22, 2025 |
| Expert Science & Technology - Quality Control, Information Technology Regular, Full time | Development | USA | East Hanover | Jul 14, 2025 |
| Sr. Specialist, DDIT OPS RLT Site ITOT Regular, Full time | Information Technology | China | Haiyan (Zhejiang Province) | Jul 11, 2025 |
| Regulatory Affairs CMC Associate Director Regular, Full time | Development | China | Beijing (Beijing) | Jul 11, 2025 |
| Protege Associate - Value and Access Early Career (Fixed Term) | Malaysia | Selangor | Jul 10, 2025 | |
| Senior Program Head Regular, Full time | Development | USA | East Hanover | Jul 08, 2025 |
| RLT Formulation Project Leader Regular, Full time | Development | Italy | Ivrea | Jul 03, 2025 |
| Therapeutic Data Strategy Director Regular, Full time | Development | USA | East Hanover | Jul 02, 2025 |
| Produktionsmitarbeiter (m/f/d), Kundl, Tirol, Austria Regular, Full time | Production / Manufacturing | Austria | Kundl | Jun 30, 2025 |
To report an adverse event or any drug related issues concerning Novartis medicinal products; please contact Novartis Patient Safety: Tel: +202 22861000 - Press 3 for reporting an adverse event.
E-mail: [email protected]
للإبلاغ عن أثر جانبى أو أي مشكلة دوائية متعلقة بمنتجات نوفارتس الطبية او الاجهزة ؛ يرجى الاتصال بقسم اليقظة الدوائية في شركة نوفارتس
+202 22861000 : الهاتف
ثم اضغط 3 للإبلاغ عن أثر جانبي +
[email protected] البريد الإلكترونى