Dhana Koteswara Rao Landa Email & Phone Number

Visakhapatnam, Andhra Pradesh, India

Vizag

Vizag

Visakhapatnam

My Position describes more about IPQA & Documentation in GLAND PHARMA LTD.

Visakhapatnam

IPQA Executive & Documnetation

Sir, I am very much enthusiastic to present this application to you with a hope that you may consider utilizing my services in your organization, keeping, in view of my versatile knowledge and commitment to work hard, dedicatedly and decisive experience in a reputed organization "CELON LABS". I enclosed here with my CV for your kind perusal. I have the capability of shouldering responsibility and flexibility of working with the people of different temperaments and sensitivity of working with utmost care swiftly. I would request you kindly provide me an opportunity to be part of your reputed organization; I assure you that I would come to the mark of efficiency deadline by superiors.

Reporting to QA manager about Production & Packing activities in Oral and Sterile Section. In-process Quality Control tests for the Oral dosage forms and sterile dosage forms, maintenance of the pertinent records.Sampling for the In-process and Finished product analysis.Ensuring the line clearance before start up of the various manufacturing operations.Online checking of the batch manufacturing recordsResponsible for ensuring the line clearance before packing.Responsible for performing the packing in-process quality control checks.Responsible for performing the rinse water sampling.Submitting finished product analysis to the QC and / or to the outside party .Collecting the finished product analysis report from QC / Microbiology and handover the same to the production department.Assisting in conducting self-inspection.Responsible for preparation of SopsResponsible for the preparation of general and new documents.Responsible for performing the process validation sampling as per the validation protocols.Responsible for preparation of validation protocols.Responsible for execution and compilation of cleaning validation.Responsible for the review of BMR & BPR, Control samples, Finished Product AuditingResponsible for initiation and Execution of Deviations related to Quality systems.Responsible for initiation and Execution of Change Controls related to Quality systems.Coordinate with other department personals to deliver the company targetsResponsible for the implementing and maintenance of cGMP in premises SkillsConsistent performer.Excellent delegation and leadership.Analysis and execution of process control techniques at the filling areas.Wastage control and monitoring Participating training and development programs.Proficiency in windows, MS word, excel

Bulk Sampling & ReleaseFinished product releaseLine Clearance In Tablet & Powder Dispensing, Manufacturing & PackingIn Process MonitoringIn Process Quality Assurance checks in Manufacturing and packingOnline IPQA DocumentationCollecting On Line Finished Samples.Product auditing.

Bulk Sampling & ReleaseFinished product release Line Clearance In Tablet & Powder Dispensing, Manufacturing & Packing In Process MonitoringIn Process Quality Assurance checks in Manufacturing and packingOnline IPQA DocumentationCollecting On Line Finished Samples

Msc, Biochemistry

Bachelor In Science (B, Bsc