About this role
Job Description
Analytical Method Development (e.g. Assay Related substance and dissolution by Chromatographic methods) Analytical method validation and method transfer. Preparation of specification, standard test procedure, Method development Reports of drug products and excipients. Maintenance and upkeep of the GLP documents. Maintain GLP environment. To provide timely support in resolving regulatory quires. To help and supports site QC investigations Work Experience 0-5Y Education Masters in Analytical Chemistry or Pharmacy Competencies