Executive - Quality Control

verified

1 - 4 Years of Experience rupess outline icon

2.00L - 3.00L Per Annum time outline icon

Full Time

Sunrise International Labs

time outline icon Hyderabad, Telangana, India

Posted on 09-12-2022

4 Vacancies

Description

Method development of tablets & oral suspensions.
Dissolution, Assay , Related substances method development and optimization of finished products.
Preparation of Analytical method development Reports.
Compatibility of API & Excipients.
Preparation of SOP’S and STP’S.
Preparation and review of Method development reports.
Preparation of stability compilation reports for finished dosage forms.
Reviewing PDR Documents.
Perform the process validation.
Perform the Dissolution profiles in different Medias.
Perform Split studies.
Performing the comparative Dissolution profiles for Generic Drug Products v/s Innovator Product with Dissolution profiles in different Medias.
Perform the compatibility studies (Filter & Tubing compatibility’s& Diluent compatibility studies)
Stability studies of Drug Products Preparation of compilation stability data of previously completed reports.
Preparation of Analytical Method Transfer Protocol and execution of method Transfer from AR&D to QC.
Calibrate the instruments according to the master calibration schedule and follow GLP and follow SOP&STP.
Maintain lab equipment’s as per GMP/GLP
Responsible for analysis, reporting of results as per procedure.
Reporting day-to-day activities to team leader.