Prepared and issued Batch Packaging Records and Master Packaging Records
Maintained inbound register by using SAP
Handled release of bulk and packaging material according to the weekly production plan
Involved in stagging activity and ensured all the packaging material and bulk was released for the production
Performed GMP related verifications such as line clearances, cleaning, room inspection, and materials
Performed physical inspection of in-process of OTC, DEA products and finished product samples
Collected the appropriately labels packaging retain samples, and submitted to the archive storage
Performed collection of retain samples for Annual Product Review
Performed sampling of Active Pharmaceutical Ingredients, excipients, and packaging components for release testing
Released completed BPR's and MPR's into the SAP
Trained in handling of Change controls, Deviations, product complaints and CAPA
Engaged in preparing training matrix of employees in the organization
Provided training for the new joinees.
Reviewed and maintained QA documentation, ensuring compliance with Standard Operating Procedures (SOPs) for completeness and accuracy
Drug Safety Associate
Vigilare Biopharma Pvt Ltd
10.2021 - 10.2022
Triage
Book-in of serious and non-serious cases
Case processing by using Argus and Clenovo databases (EVWEB cases, Spontaneous case, Pharmaceutical company cases, Business partner cases, Pregnancy registry cases and Clinical trial cases)
Retrieving and reconciling of data from source documents in follow-up cases
Preformed quality review of spontaneous cases
Skilled in GvP, GCP, Standard Operating Procedures, CAPA management, Deviations and change control
Preformed reconciliation activity by using Argus database
Trained junior associate regarding the case processing and quality check
Clinical Pharmacist Intern
Guntur City Hospitals
11.2020 - 11.2021
Practically trained in clinical pharmacy services in departments including Nephrology, Infectious disease, Pulmonology, Intensive care unit, pediatric and orthopedic
Internship activities were primarily focused on the Interpretation and analysis of patient information - active disease conditions list, past medical history, physical exam data, laboratory data, hospital course, medication history, medication profile, and pharmacokinetic evaluation
Reviewed medication orders for appropriate dose, duration, frequency, dosage form, indication, and drug interactions
Collaborated with hospital pharmacologists in developing medication error statistics in tertiary care hospitals in the past 2 years and classified which department and drug class to focus on