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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.

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AUXILLA Pharmaceuticals Hiring M.Sc / M.Pharm