Company: AUXILLA Pharmaceuticals And Research LLP
Location: [Specify Location]
Position: Research Associate – QA Department
Experience: 2-4 years
Qualification: M.Sc / M.Pharm
Job Responsibilities:
- Prepare and review Method Development (MD) & Method Validation (MV) reports and protocols.
- Prepare and review Standard Test Procedures (STPs), Standard Operating Procedures (SOPs), and compile stability data.
- Review batch documents to ensure compliance with company standards.
- Review product development reports and related documents.
- Prepare method transfer protocols and reports.
- Maintain documentation control and ensure accurate record-keeping.
Required Skills:
- Strong understanding of MD & MV processes.
- Proficiency in preparing and reviewing STPs, SOPs, and stability data.
- Experience in reviewing batch documents and product development reports.
- Expertise in documentation control and method transfer protocols.
- Attention to detail and excellent organizational skills.
How to Apply: Interested candidates are encouraged to share their CVs with us at hr@auxillapharma.com.