Diploma

Execute the production planning in Liquid manufacturing block and ensure the production plan achievement as per plan. Responsible to ensure the entry and exit, gowning and personnel hygiene procedures are followed in liquid manufacturing block.

Seeking a dynamic independent and experienced Research Associate in Clinical Management for processing, reviewing and receiving clinical data and records and from therapeutic groups as well as internal and outside investigators. Ensuring accurate, timely, and consistent data reaches the clinical teams and other groups. Master degree in pharmacy/ life science/Biology/Biotechnology/ Biochemistry/Diploma in Clinical Research

Diploma/D. Pharmacy/B. Pharmacy; Operating Granulation, Compression, Coating, Capsule Filling, Blister & Bottle Packing Equipment. Supervising Granulation & Packing Lines. Experience in Autoclave, Filling, Vial Washing, Packing Areas

M.Sc, M.Tech, B.Pharm having 2 to 6 years of experience of Biotech and Chemical Analysis e.g., Electrophoresis, Bioassay, HPLC & GC.

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.

Bachelors Degree in life sciences with Full Time Post Graduate degree in Hospital or health care from a recognized university. At least 1 Year of experience in Hospital after acquisition of the aforementioned qualifications

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.

Postgraduate, Graduate degree in Science Eg. B.Pharm, Life Science, B.Sc., Biotech, Zoology, Botany, etc. with Diploma in Clinical Research is mandatory. One year experience in clinical trial monitoring is desirable.

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