QC Tech Writer
Job Summary
• Crete new test methods based on Current USP or In-House method
• Write Method validation protocols for Assay, Impurity, dissolution and Residual solvent Methods
• Write method validation reports for the Assay, Impurity, dissolution and Residual solvent Methods
• Initiate additional report required for the submission, as required
• Initiate CC for the Test methods and specifications, as instructed by supervisor
• Track the test method numbers, protocol and Report Numbers per SOP
• Co-ordinate with Lab Manager or Department head regarding the test parameter requirements
• Responsible if the method validation protocols are per meet the ICH guidelines
Reporting to:
- Lab Manager or Department Head.
To apply, please submit résumé referencing job code MAC004 to HR hr@aavispharma.com, Aavis Pharmaceuticals, 9488 Jackson Trail Road, Hoschton, GA 30548.