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