Job Description
We are seeking a diligent and detail-oriented Regulatory Affairs Associate to join our Greater Noida office. This role involves managing registration processes and regulatory submissions for Medical Devices, In-Vitro Diagnostics (IVDs), and Cosmetics. If you possess a deep understanding of industry regulations and have strong communication and organizational skills, we encourage you to apply.
Key Responsibilities
- Registration Management: Oversee and manage registration processes with the central licensing authority.
- Document Preparation: Compile, prepare, and review documents for application submissions.
- Query Handling: Address and resolve regulatory queries related to submissions.
- Client Interaction: Engage with clients, providing updates and support throughout the regulatory process.
Requirements
- Educational Background: M.Pharm. preferred.
- Experience: 1-2 years in regulatory affairs, particularly in Medical Devices, IVDs, or Cosmetics.
- Technical Skills: Proficiency in Microsoft Word and Excel.
- Regulatory Knowledge: Strong understanding of regulatory guidelines and industry standards.
- Communication Skills: Excellent oral and written communication skills, with attention to detail.
How to Apply
Interested candidates should email their resume to info@regulatory-solutions-india.com.
Job Category: Regulatory Affairs
Job Type: Full Time
Job Location: Greater Noida