Prakash Mohan Saroj

With nearly 11 years of successful experience in quality management functions across the pharma/consumer drug lifecycle, I am an analytical and quality-oriented professional with a keen eye for detail. Throughout my career, I have led various functions including calibrations, testing, stability analysis, investigative analysis, GLP activities, and review of analytical documents. As a valuable team member, I have successfully handled regulatory and customer audits, ensuring compliance at all times. My track record includes implementing standards to continuously improve product quality and services. I possess a creative problem-solving approach and maintain an energetic and eager attitude towards learning new processes and skills.

• To Review analytical document of finished product, raw material, packing material, in-process product once it was reviewed by QC department.
• Daily calibration of balance, pH meter, KF factor and temperature monitoring etc.
• Sometimes if required I will prepare Analytical method Validation, Transfer or Verification protocol.
• To Prepare Report of Analytical method Validation, transfer or verification after completion of successfully execution.
• To participate in investigation of the OOS, OOT deviation/incidences, non-conformances as an investigation team.
• Assign a CAPA, close the Incident, deviation, Change control or QMS documents.
• Prepare a trend analysis, OOT, define a limit for tests.
• Work in teams. Work along with cross-functional team.
• Work by adhering to discipline of the site and organization.
• Protect the property of the organization.

• HPLC (Shimadzu LC 2030, Shimadzu LC 2010, Thermo Dionex Ultimate 3000, Water, Agilent 1260)
• UV-Vis Spectrophotometer (Shimadzu)
• KF-Metrohm Apparatus
• Dissolution test Apparatus (Electrolab, Lab India)
• Electronic Balance (Mettle Toledo, Radwag)
• Auto Titrator - Metrohm
• FTIR (Perkin Elmer)

• Age: 33
• Date of Birth: 02/09/91
• Gender: Male
• Nationality: Indian
• Marital Status: Married (Have 1 Son)