QA

Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule. Carry out routine analysis & Ensure documents pertaining to day to day analysis.

Reviews all Annual Product Quality Review APQR reports received from manufacturing partners and prepares APQR reports other than those received from the manufacturers within the prescribed time frame.

Good exposure require in IPQA - Sterile, Qualification Sterile & OSD & Documentation Cell. Finished, AMV & Stability Section, knowledge of Instrument - HPLC. GC. Preferably know-how of Chromeleon Software.

B. Pharma. /B.Sc. Biotech./B.Sc. Medicinal Chemistry/B.Sc. Pharmaceutical Chemistry M.Pharma/M.Sc. Biotech /M.Sc. Medicinal Chemistry /M.Sc. Pharmaceutical Chemistry. To assist in preparation of purchase orders and send copies to suppliers and to departments originating requests. Follow up with suppliers in respect of timely supplies of products with respect to the issued purchase orders. 

SCIENCES, PHARMACY GRADUATES B.SC, M.SC, B. PHARM, M. PHARM WITH 0 TO 3 YEARS EXPERIENCES IN ANY OF QA FUNCTION VALIDATION, IPQA, QMS, COMPLIANCE, DQA, LAB QA OF A FORMULATION - STERILE, NON STERILE DOSAGE

B.Pharm/ M.Pharm / M.Sc; Hiring for SEZ 1 OSD Manufacturing Unit, Ahmedabad. IPQA / equipment qualification /QA QMS; Granulation, IGL, Compression, Coating, Wurster coating, Capsule filling

B.Pharma / M.Pharma / M.Sc.; Experience in Quality Assurance QMS, AQA, Process Validation, IPQA, RACoordinator, Training, Computer System Validation. Macleods Pharmaceuticals Ltd. is one of the fastest growing pharmaceutical company.

B.Pharma, B.Sc., M.Sc.  Granulation, Compression, Coating, Continuous coater, Capsulation, Press-fit, Inspection. Blister Packing, Bottle Packing, Bulk Packing. Exhibit/IP/FP, Hold Time, Stability, Vendor Qualification, Method Validation and GLP, RM, PM, VQ, Sample Management

Manufacturing, filtration, filling, Lyophilization, sealing, and pre- and post-manufacturing activities. Planning and execution of batch manufacturing activities, filling activities, lyophilization, sealing activities, and filter integrity. Monitoring NVPC and trending.