Ravi K. Rana

• Presently I am working with Synthimed Labs Private limited formerly known as Ind-Swift Laboratories Limited R&D as a RQA (Research Associate II) in Research Quality assurance department from Nov 2024 to till date…..SAS Nagar ,Mohali Chandigarh.
• Job Responsibilities in Synthimed Labs private limited:-
• Issuance of documents like sop,spec/stp and AMV Protocol , Reports and General Report.
• Review the AMV Protocol and Reports.
• Review the calibration and preventive maintenance schedule.
• Review the Technology Transfer Documents.
• Review the process validation Protocol and Reports.
• Investigation the Deviation, out of specification and out of trend.
• Review the documents of vender Qualification.
• Review the Amendment, incident and Non-Conformity.

Job Responsibilities in IPCA Laboratories Limited:-

• Review the Analytical data of Raw material, In-process, Intermediate, finished products (Instrument and wet analysis).
• Review the Analytical data of process validation, Analytical method validation, cleaning validation, Analytical method transfer.
• Review the electronic audit trail reports, before batch release.
• Review of Instrument calibration Record.
• Review the Instrument usage log books.
• Review the HPLC and GC column usage log books.
• Review the working standard consumption record.
• Review the primary standard consumption record.
• Review the daily monitoring of temperature record of rooms.
• Review the Control sample record.
• Review the sampling activity of raw materials, packing material, finished product and finished intermediate records.
• Review and monitor the Quality management system activity like OOS/OOT/OOC/Incidence.
• Review of new prepared and revised specifications, method of analysis and test data sheets.
• Review of External calibration record.
• Any other Assignment given by Lab in charge/Manager Quality Control from time to time.

• Job Responsibilities in Zydus Healthcare Limited:-
• Prepare the purchase requisition as per requirement and make a GRN as per appropriate process
• Handling the Quality Management System and Good Document Practices like Deviation , Out of Trend and Out of specification etc.
• Responsible for the calibration of instruments.
• Sample analysis of MDI ( Metered Dosage Inhaler) and also have physical parameters.
• The reference standard inward and issuance record and HPLC column are inward record and maintained , dedicated products as per requirement.

• Job Responsibilities in Torque (Torex) Pharmaceuticals pvt Ltd:-
• Responsible for QC testing of In process(Bulk) product and finished product and also as stability (Raw material HPLC Testing, Tablets, Capsules like Hard Gelatin and soft Gelatin, Topical (Ointment), and Oral liquid.
• Preparation of samples of Gas Chromatography and Atomic Absorption spectrophotometer.
• Log book entry and related documentation to be make online.
• Support to prepare drug substances and drug product testing and its release with all documents.
• Handle the instrument and equipment for routine use as well as calibration and qualification.
• Prepare the Standard operating procedure, Standard Test Procedure ,General Test Procedure and Test Data Sheet as per requirement.

GPA: 78.7%