QA

B.Pharmacy / M.Pharmacy; Candidate should have Injectable experience and sound knowledge on manufacturing and packing activities of liquid and Lyo products. Aseptic process simulation, process validation, cleaning validation, Batch records review and batch release.

Centre of Excellence on Phytopharmaceuticals and Herbal Products; Ph.D. in Pharmaceutical Sciences or Analytical Chemistry, Pharmaceutical Analysis with first class post- graduation in M.Sc. Analytical Chemistry, Organic Chemistry or M.Pharm, MS.Pharm Pharmaceutical Analysis, Quality Assurance, Natural Products, Medicinal Chemistry; Hands on experience for operation and analysis of HPLC and different chromatographic instruments.

B.Sc / M.Sc / B.Pharma / M.Pharma; Review HPLC methods, chromatograms, and system suitability. Ensure HPLC sequences comply with methods. Prepare and review IQ, OQ, and PQ for new instruments. Conduct pre-investigations for OOS, OOC, OOT, and lab incidents. To perform line clearance, FG Sample withdrawal, Online GMP Monitoring, To Support of Product and Process Validation

Supervision of Micro Section Microbiological Analysis of Raw Material, Finished Product, Water Samples, Stability ad Hold Time study Samples. Review and Verification of Micro documents, Preparation of Protocols and SOP, QMS, Environment Monitoring Media Preparation, GPT Test, Microbial, Limit Test of Finished Product and Raw Material, Water Testing etc. - Calibration and Validation of Microbiological Instruments.

HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should also have knowledge of weight analysis, stability studies, for Injectable dosage forms.Also require candidate with experience of Bio Assay QMS and analytical data Review. B.Pharm / M.Pharm. Supervising and Controlling Production areas like Isolator, Aseptic Filling, Vial Washing, Autoclave, Lyophilizer and Visual Inspection. Should have knowledge of QMS activities.

Pharmaceutical Chemistry, Pharmaceutical Analysis, Quality Assurance, Pharmaceutics; Kota College of Pharmacy emphasizes on the overall development of the students since last 18 Years. It aims at not only producing good pharmacist but also good and worthy citizens of the society.

GLP, Raw Material -Packaging Material, In Process-Finished Product, Method Verification Protocol preparation & Document Section Knowledge required; Water sampling/testing, EM Observation, Culture Handling, Media Management, Having Digital exposure for LIMS/ MODA Software B.Sc/ M.Sc/ B.Pharm; Lead QC operations as Shift In-Charge. Review analytical data, Ensure compliance with LIMS, GLP, ALCOA ICH/FDA

Apprenticeship Program is specifically designed for fresh graduates like you to learn from industry experts, gain hands-on experience, and contribute to our mission of saving and sustaining lives. Fresher or less than 1 year of work experience; Graduated in the last 4 years. 2021 or later.

FP / Stability / Analytical Instrumentation-HPLC, UV and Dissolution; Handling of LIMS, Empower software, HPLC Waters; IPQA Mfg. and Packing, Shop floor activities. Review of equipment audit trails / BMR, BPR review / line clearance. Handling of CAPA / EC and External Audits USFDA/MHRA/Germany