SP Accure Labs Hiring Regulatory Affairs (Oncology/General Medicine)
**SP Accure Labs** is seeking experienced Regulatory Affairs professionals to join our team. If you have a strong background in dossier filing and CMC handling, particularly in oncology or general medicine pharmaceuticals, this is an excellent opportunity to contribute to a company dedicated to “Touching Lives Globally.”
Join SP Accure Labs: Touching Lives Globally
**SP Accure Labs** is committed to developing and delivering high-quality pharmaceutical products that improve patient lives worldwide. We are looking for talented individuals to join our Regulatory Affairs team and play a crucial role in ensuring our products meet regulatory requirements across global markets. This is your chance to be part of a team that is making a difference in the healthcare industry.
Position Available: Regulatory Affairs
Experience
- 4-10 Years of relevant experience.
- Preferred experience in Oncology or General Medicine Pharmaceuticals.
Qualification & Skills
- Filing Dossiers & Deficiencies (EU & ROW).
- Dossier Compilation & Review (EU Marketing Authorization).
- CMC Handling for Multiple Drug Products.
- CMC Module Preparation & Compilation (Formulations).
- Review of Development Reports & Validation Protocols.
How to Apply at SP Accure Labs
Interested candidates can apply through the following methods:
- Call us at: 73966 44772
- Send your CV to: jobs@spaccurelabs.com
Join **SP Accure Labs** and be a part of a team that is dedicated to improving global health. Find regulatory affairs jobs and pharmaceutical jobs here.
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