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| Job Title Sort ascending | Business | Location | Site | Date Posted |
|---|---|---|---|---|
| QC Analyst II 正式, Full time | Quality | China | Changping County (Beijing) | Jan 21, 2025 |
| TRD RLT Senior Expert Isotopes (m/f/d) Regular, Full time | Development | Italy | Ivrea | Jan 17, 2025 |
| Sr. eCompliance Specialist Regular, Full time | Quality | India | Hyderabad (Office) | Jan 08, 2025 |
| Manufacturing Data System Expert Regular, Full time | Production / Manufacturing | India | Hyderabad (Office) | Jan 07, 2025 |
| Sr. Spec. DDIT GF Sol.Del. HCM Regular, Full time | Information Technology | India | Hyderabad (Office) | Jan 07, 2025 |
| Specialist - MS&T Regular, Full time | Production / Manufacturing | India | Hyderabad (Office) | Dec 20, 2024 |
| Assistant Manager SOD Ops Regular, Full time | Finance | India | Hyderabad (Office) | Dec 19, 2024 |
| Global Program Regulatory Manager- LCM Regular, Full time | Development | India | Mumbai (Office) | Dec 12, 2024 |
| RA CMC Manager Regular, Full time | Development | India | Hyderabad (Office) | Dec 03, 2024 |
| Senior GCP/PV Auditor Regular, Full time | Other | India | Mumbai (Head Office) | Dec 03, 2024 |
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