QC

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

Manage granulation, compression, coating, pelletization and capsule filling area. Manage bulk bottle, blister packing. Track and Trace, serialization and documentation. Handle machines like CVC, Servo, Countec, CAM, BQS, HONGA & UHLMANN.

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.

Lab experience for Analytical Method Development, regular and stability sample analysis. Handling of HPLC for Assay, Dissolution, Related substances tests for solid orals. Perform pre-formulation studies, R and D trials and support scale-up activities Conduct R and D trials for oral solid dosage forms tablets, capsules, etc. M.Pharm / MSc

B.Pharm / M. Sc. Analytical Chemistry. Experience or Fresher Can also Apply; Preparation of Specifications in LIMS. Preparation of Methods in LIMS. Preparation of Standard Testing Procedures in LIMS.

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.

Qualification B.Sc, B.Pharmacy, M.Sc, M.Pharmacy; MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India and USA.