Analyst-HPLC

Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices. Responsible to perform the Analytical method validation, method verification and method transfer activities.

Role SummaryThe Analyst will be responsible for performing qualitative and quantitative analysis of pharmaceutical raw materials, intermediates, and finished products using Reverse-Phase High Performance Liquid Chromatography (RP-HPLC) and other analytical techniques. The role ensures compliance with GMP, regulatory standards, and company quality systems.Key...

Technical Expertise:Hands-on experience with HPLC, UV, IR, GC instrumentsStrong understanding of GMP complianceKnowledge and adherence to Data Integrity principles (ALCOA/ALCOA+)Audits Faced:Involved in facing regulatory and internal audits such as:USFDA / MHRA / WHO / GMP / ISO (mention whichever apply for the candidate)Supported audit preparedness,...

Summary:1. Calibrate, operate, and maintain analytical instruments like HPLC, GC, UV, FTIR, and Karl Fischer.2. Hands-on experience in HPLC, GC.3.Analysis of raw materials, intermediates, and finished products using HPLC, GC & other instruments. Required Candidate profileNote: Only for MALE candidates with Pharma Bulk Drugs & Intermediates experience and...

Raw material inproses sample Intermediate samples and Finished samples HPLC reviews and wet analysis reviews and instrument calibrations reviews and handling planing analysis

Job DescriptionThe QC Analyst will perform routine analytical testing of raw materials, in-process samples, finished products, and stability samples to ensure compliance with quality standards. The role involves operating analytical instruments, documenting results as per GLP/GMP, and supporting laboratory investigations.Key ResponsibilitiesConduct testing...

Hands-on experience in HPLC/GC/LC-MS/GC-MS including method development, routine analysis and method validations along with good documentation practices.Candidate should have good scientific knowledge.Candidate should have proper knowledge on all the regulatory guidelines including USP/EP/IP/WHO/Brazil/China pharmacopeias. Role & responsibilities

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

KRA'sDevelop innovative formulations to expand the product portfolio and address evolving market demands Key Skills/Abilities Proficiency in operating and interpreting results from HPLC, UV-Vis Spectroscopy, and Karl Fischer titrationPerform analytical testing of premixes: HPLC, UV-Vis spectroscopy, Karl Fischer titrationCollaborate with production teams on...

Job Summary:Responsible for leading all Quality Control (QC) activities for sterile injectable products. This includes ensuring cGMP compliance, timely testing of materials and products, method validations, and lab readiness for audits and inspections.Key Responsibilities:Oversee day-to-day QC lab operations for sterile injectables (raw materials,...