by maheshbhuva | May 28, 2026 | 483 observation, ALCOA++, Analytical method development hplc,, Hplc, Job interview, News Pharma, Pharmaceutical interview,
STEP-BY-STEP PROCEDURE 1. PURPOSE To describe the steps for initiation, investigation, implementation, effectiveness check and closure of Corrective and Preventive Actions (CAPA) in QMS to ensure product quality and compliance with regulatory requirements. 2. SCOPE...
by maheshbhuva | May 20, 2026 | Analytical Chemistry, Out of specification, Pharmaceutical interview,, Quality control (QC)
Can we average an OOS result with passing retest results to get a passing average? A: Absolutely not. Both FDA and MHRA guidelines strictly prohibit averaging an OOS result with passing retests to “hide” the failure or bring the batch into compliance....
by maheshbhuva | May 19, 2026 | Analytical Chemistry, Documents error (DIN), GMP, ICH Guideline, Out of specification, Pharmaceutical interview,, QMS, Quality control (QC)
An Out of Specification (OOS) investigation is a critical regulatory requirement in the pharmaceutical industry. When an analytical result falls outside the established specifications or acceptance criteria (defined in pharmacopoeias, drug applications, or internal...
by maheshbhuva | May 16, 2026 | Hplc, Hplc column, HPLC VIAL, Job interview, Pharmaceutical interview,, Quality control (QC)
In the competitive landscape of modern pharmaceutical companies, ensuring precise product quality isn’t just a regulatory requirement—it is the foundation of patient safety. At the heart of this quality assurance is HPLC analysis (High-Performance Liquid...
by maheshbhuva | Apr 22, 2026 | Analytical Chemistry, Career, Career and Mental Health, News Pharma, Out of specification, Pharmaceutical interview,, Quality control (QC), wet lab
Finding pharmaceutical jobs outside of India requires looking at specific global platforms that specialize in life sciences. Since you have experience in Quality Control (QC), you can find many opportunities in manufacturing hubs like the USA, Europe (Germany,...
by maheshbhuva | Mar 26, 2026 | Analytical Chemistry, Analytical method development hplc,, Hplc, Hplc column, Pharmaceutical interview,, Quality control (QC)
HPLC column HPLC columns are classified in the United States Pharmacopeia (USP) under the “L” designation system, with each type assigned a specific USP code (e.g., L1, L3, L7). The main USP chapter that governs chromatography, including HPLC columns, is USP...
