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

 

To apply, please submit résumé referencing job code MAC004 to HR hr@aavispharma.com, Aavis Pharmaceuticals, 9488 Jackson Trail Road, Hoschton, GA 30548.