Roles & Responsibilities :–
Working on Analytical Method Development of dosage forms like Oral Solids (Tablet & Capsules)&ndash IR tablets, Sustained release tablets, extended release tablets, Bilayer tablets, Capsule etc. & External preparations like Gels, Pastes, Creams, Ointments etc. under guidance of Team lead to find optimal Analytical method.
Performing analysis of In-process samples & finished products samples of trial batches of F&D and finalised formulation stability study sample analysis.
Performing Dissolution profile, pH & Solubility Study, Stability study of trial product and raw materials in wet lab & instrument lab.
Properly documenting activities of the project under investigation under guidance of Team Lead.
Preparing AMV and AMT protocols and reports as per regulatory and customer requirements under guidance of team lead.
After finalization of method, Executing Analytical Method Validation as per guidance of Team lead.
In case of absence of samples from F&D, performing QC routine analysis of RM, In-process & finished products.
Performing analysis for Cleaning Method validation.
Following QC SOP&rsquos, Good Laboratory Practices & Safety norms while working in Lab.
Performing working instrument calibration as and when required.
Highest Qualification :–
M.Pharm / M.Sc
you can mail your resumes on [email protected]