Suraj Ranshing

Quality Control (Pharmaceutical)

Talent

BoisarMember since October 9, 2026

HPLC analysisChemical analysisPacking material testingStability sample managementAnalytical testingDocumentationReconciliationsChamber maintenanceIn-use stability studyHPLCRegulatory and customer auditsLoan licence auditsMaster ControlcGMPGLPALCOA++ principleQMSCAPALIMSAuditSOPsSpecificationsSTPTDSProtocolsDeviationOOS/OOTMSDS

Hire this person

Send a job offer directly to this candidate

HPLC analysisChemical analysisPacking material testingStability sample managementAnalytical testing

About

A competent professional with leadership qualities, problem solving skills and expertise in the domain provided. In quest of challenging opportunity in an organization of repute. I desire to take my career to the pinnacle of success by setting high standards of performance and achieving my goals as an objective.

Organizational Experience: About 8.0 Yrs. I have experience of HPLC analysis & Chemical analysis. Also I have experience of Packing material testing. Handled the stability section including stability sample management, analytical testing, documentation, reconciliations, chamber maintenance and In-use stability study.

Audit Experience: Experienced in handling and supporting regulatory and customer audits like WHO, EU-GMP, Russia, INVISA, INVIMA, Canada, Nigeria, Uganda, Ukraine, PICS. Also facing loan licence audits like Cipla, Dr.Reddy’s, Alkem, Mylan, Sun pharma, Zydus, Hetero, NATCO.

Experience

Quality Control Executive - V.S.International Pvt. Ltd. - Tarapur

(2025-09)

A progressive company dedicated to the OSD formulation (Tablets & Capsules).

Currently working in HPLC Section as a Operator and perform analysis of Finish product, Raw material, Stability & Intermediate samples.
Perform Calibration of HPLC as per schedule.
Responsible for daily perform integration of HPLC and reporting on time.
Responsible for review sequences of HPLC in absence of reviewer.
Responsible for preparing, verifying and maintaining SOP’s, Specifications, STP, TDS & Protocols as per cGMP & GDP.
Support and assist QMS activities, documentation and compliance activities.
To allocate work to analyst in absence of section head.
Receiving the Intermediate and Finish samples in section along with respective entries in logbooks.
Responsible to follow GLP procedure, facility and document updating as per committed.
Responsible for maintain documents and follow ALCOA++ principle.
Maintaining & handling the quality control records.
Accountable for accurate and timely analytical testing, reporting and release of raw material, inprocess, finish product and stability products.
Accountable for compliance with cGMP, GLP, SOPs, and data integrity requirements.
To follow ALCOA++ principle.
Accountable for proper operation and documentation of laboratory instruments.
Timely completion and support for deviations, CAPA and QMS related activities.
To follow safety rules, guidelines, MSDS and maintain the laboratory safety.
Coordinate calibrations and maintenance of laboratory instruments.
To ensure that valid working, reference, impurity standards are used for analysis.
To report any incidents/OOS/OOT/Deviations in time to the section head.
Execute LIMS activity as per LIMS role & Master control role & ERP Value recording.