Senior Executive-QC

Piramal Pharma Ltd; Indore District; On-site; INR 500,000 - 700,000; Full time

Job summary

Piramal Pharma Ltd is seeking a Senior Executive-QC (ICPMS Analyst) in Indore to perform ICP-MS and LC-MS analyses for in-process materials, raw materials, intermediates and finished products, ensuring timely dispatch as per the monthly schedule. The role includes method development, validations, transfers, and real-time data monitoring.

The candidate will review reports, manage calibration certificates, maintain instrument readiness, and train contract personnel in glassware cleaning and

Qualifications

• Experience with ICP-MS and LC-MS instrumentation.
• Analytical method development, validation, and transfer.
• Knowledge of GLP/GMP and QA procedures.

Responsibilities

• Perform ICP-MS and LC-MS analyses for in-process, raw materials, intermediates, and finished products.
• Prepare and review protocols, worksheets, and reports for methods and transfers.
• Ensure documentation, calibration, and instrument maintenance are up to date.
• Release batches on time to support production schedules.

Skills

ICP-MS analysis

LC-MS analysis

Analytical method development

SOP compliance

Education

M.Pharm / B.Pharm in Pharmaceutical Science

Tools

ICP-MS

LC-MS/MS

Job description

Senior Executive-QC (ICPMS Analyst)

• Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPL.
• Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule.
• Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS.
• Responsible to prepare and review the protocols, work sheets and reports for method developments, method validations verifications and transfers
• Responsible for allotting the work to the chemist within the section.
• Responsible for performing the calibrations of all instruments in section as per the schedule.
• Responsible for maintaining all the documentation online.
• Responsible for maintaining the minimum stock for working standards, reference standards and impurity standards and ordering as and when required.
• Responsible for maintaining the minimum stocks for chemicals, reagents, glass wares and solvents required for analysis.
• Responsible for keeping instruments neat and clean and overall housekeeping in the section.
• Responsible for review of analytical data, calibration data, qualification data
• Responsible for keeping all instruments within the calibrated status.
• Responsible to do the analysis, review and release on time to support the production
• Responsible for reducing the lab incidences, repeat analysis and no Data Integrity issues.
• Responsible for real time data monitoring.
• Responsible for reviewing the analytical data received from external laboratory.
• Responsible for maintaining all the calibration certificates, qualification certificates, standard weight certificates and working/reference standard certificates.
• Responsible for maintaining the consumption records and traceability of working/reference standards.
• Responsible for OOS investigations, OOT, OOC and deviations investigations and CAPA implementations
• Responsible for review of SOP’s , test procedures and specifications
• Responsible for providing the training on GLP/GMP to the employees working the section.
• Responsible for releasing the batches timely manner to achieve the site requirement.
• Responsible for preparing the COA’s as per the customer requirement
• Responsible for approving/rejecting the batches in SAP
• Responsible for Controlling the cost and operate within the approved budget.
• Responsible for maintaining the instruments in working condition and reduce the breakdown time of instruments.
• Responsible for carrying out the analytical method transfers.
• Responsible for keeping the critical spare parts of the instruments.
• Responsible for Safe working conditions and clean environmental practices.
• Responsible for usages of required safety appliances in the section.
• Responsible for SFTI.
• Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches
• Responsible for training the contract persons and helpers on glassware cleaning.