Pharma Analytical Validation Method

Plan, execute, and document analytical method validation (accuracy, precision, specificity, linearity, robustness, LOD/LOQ, etc.) for raw materials, in-process samples, finished products, and cleaning validation.
- Review and approve validation protocols and reports in compliance with ICH Q2(R1), USP, and other regulatory requirements.
- Ensure all AMV activities meet GMP, GLP, and cGMP guidelines.
- Coordinate with R&D, QA, and Production teams for smooth tech transfer and validation support.
- Troubleshoot analytical method issues and recommend improvements or revalidations when necessary.
- Maintain and calibrate analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
- Prepare for and participate in regulatory inspections and internal audits.
- Train and mentor junior QC staff on method validation procedures and regulatory expectations.
- Ensure all documentation is complete, accurate, and archived as per SOPs.

**Job Location**:Giloth **(Neemrana Rajasthan)**

**Experienced Only Required**

**Job Types**: Full-time, Permanent

Pay: ₹20,000.00 - ₹35,000.00 per month

**Benefits**:

- Commuter assistance
- Food provided

Schedule:

- Day shift

Supplemental Pay:

- Overtime pay
- Yearly bonus

Work Location: In person