Job Title: Research Associate (Analytical Document Review)
Company: AUXILLA Pharmaceuticals And Research LLP
Department: Analytical Development (AD)
Experience Required: 2 – 4 years
Qualification: M.Pharm
Key Responsibilities:
- Prepare and review Method Development (MD) and Method Validation (MV) reports and protocols.
- Prepare and review Standard Test Procedures (STPs), Standard Operating Procedures (SOPs), and compile stability data.
- Conduct literature searches for analytical methods.
- Prepare method transfer protocols and reports.
Skills Required:
- Proficiency in preparing and reviewing analytical documents such as MD, MV, STPs, SOPs.
- Experience with stability data compilation.
- Strong literature search skills for analytical methods.
- Ability to prepare method transfer protocols and reports.
Application Process:
Interested candidates are invited to share their CVs via email at hr@auxillapharma.com.
