Company Jobs

Coordinate with QC Analytical, ADL, R&D, and Stability teams. Perform gap assessment against target market regulatory requirements.

Good understanding of regulatory framework, including regional trends, for various types of applications and procedures for small and large molecules across all regions as well as knowledge of global pharmaceutical legislation and guidance specifically linked to regulatory CMC aspects in the ICH countries.

Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling.

Expertise of Analytical techniques like Assay, Dissolution, CU, BU, RC test etc by HPLC,GC,U V,UPLC,FTIR,KF Titrator, PSD etc

Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity

Process check & sampling during manufacturing and packaging. Review filled Batch manufacturing & batch packing record.

B.Pharma/M.Pharm walkin at Lupin pharma. Experience specific of QAMS, Handled software for QMS change control, Regulatory expectations/Validation, Qualification equipment / utilities / software Investigation

Development of simple and complex parenteral & ophthalmic formulations - Generic & 505(B)(2), Conduct literature research and evaluate new technologies / excipients.

Strong knowledge and expertise in chromatography and working as an analytical scientist with a multinational pharma / FMCG organization, particularly with experience in stability testing.