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