B.Tech

Conduct QC testing on raw materials, packaging, stability, in-process, and finished products. Capable of Handling Instrument like HPLC, GC, IR,UV instrument. Knowledge of Dissolution tester, KF, Potentiometer.

Carrying out research and experiments related to the project. For example, fabrication, characterization, and performance optimization of sensors. Analyzing and interpreting data, documenting research findings. 

Graduate in Science, Engineering, Pharmacy with Post-Graduate Diploma, B-Tech in Packaging from 11P or a reputed institute.

Doctoral Degree in Science from a recognised university or equivalent in Biochemistry, Biotechnology, Stem Cell Biology and Neurobiology, Neuroscienc e with a strong publication record and research experience in Cell Biology, Molecular Biology and Neurobiology.

B.Pharm, M.Pharm, B.E, B. Tech with 6 to 10 years of experience in Supervising and Controlling Production areas like Aseptic Filling, Vial Washing, Autoclave, Lyophilizer, Visual Inspection and Packing. Should have knowledge of QMS activities

Individuals desirous of seeking admission to PhD program at NIAB must have a Masters degree M. Sc., M. Tech., M. V. Sc. or M. Pharm or MBBS or B. Tech. degree in any branch of Life Science. Candidates must mandatorily have secured CSIR, UGC, DBT, ICMR, INSPIRE NET JRF, UGC-RGNF

Responsible for process validation and cleaning validations and respective documentation. Responsible for Equipment and utilities qualification and periodic validation.

Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca'a API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.

M.Sc. Biotechnology Microbiology, M.Tech, B.Tech Biotechnology Bioprocess Engineering, M.Pharm Experience 3-10 years of experience in Drug Substance and Drug Product and In-Process Quality Assurance, QMS Deviation, Change Control, CAPA, Investigation, APQR, CPV, Process Validation, and Cleaning Validation