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Candidate should have exposure in analysis of Content Uniformity, Blend Uniformity, Hold Time Study, Cleaning Validation Test and Finish Product Analysis.

Exposure of analysis for Finished Products, Stability Samples & Raw Materials. Having Knowledge of Analytical Method Validation, Verification & Method Transfer. Having skill for data interpretation, troubleshooting. Pharma knowledge of Solid orals & Quality process.

Post Graduate degree in plant Biotechnology, Plant Molecular Biology, Plant Molecular Biology and Biotechnology, Agricultural Biotechnology, Plant Sciences, Biochemistry, Life Sciences

M.Sc. with atleast 55% Marks in Life Sciences, Zoology, Animal Biology, Biotechnology, Biochemistry, Human Genetics, Molecular Medicine,Pharmaceutical Sciences, Chemical Sciences from any from any UGC recognized University/Institute. 

M.Pharm, B.Pharm, MSc Chemistry, Biotechnology, Life science, Microbiology, BSc, B.Tech Electrical, Mechanical, Instrumentation, Biotechnology, Diploma.

M.Pharm, M.Sc, B.Pharm, B.Tech, B.Sc, D.Pharma, Diploma, ITI, 12th Only Pharma Background Candidates can apply; OSD- Granulation, Compression, Coating, Capsule, Blister, Alu- Alu, Strip, Auto Cartonator; Sterile Manufacturing, Filling & Sealing, Autoclave, CNC, Washing & tunnel, small scale and Lyophilization

BPharm / MBBS / Integrated BS-MS / MSc / BE / BTech; Identifying the role of host F-box proteins, a component of E3 ubiquitin ligase complex, in HIV-1 pathogenesis and their potential use as therapeutic target against the virus. Investigating the role of clathrin light chain in neural development and function.

B.Pharm with minimum 1-year experience OR D.Pharm with minimum 3 years working experience in Dispensary, Pharmacy of the Hospital having minimum 200 beds.

Experience in reviewing specifications and STPs, ensuring data integrity, proposing QbD Quality by Design process changes, and participating in phase gate reviews