Syngene

Responsible for operation and cleaning of Automatic visual inspection machine and labelling machine for DP. Preparation, review and execution of Study protocol / SOPs / QRM / Study report / QRM report in the drug product facility.

Analytical Research and Development enabling Chemical Development and API Supply. Routine analysis of in-process and isolated samples for early intermediates and APIs using chromatographic and wet analytical techniques

Looking for M.Sc with 6-17 yrs experience & M.Pharm with 5-15 yrs experience. The candidate should have a good educational and theoretical, analytical chemistry background.

Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group to accomplish the tasks in a timely and efficient manner.

Masters degree/ bachelors degree in pharmacy, Masters degree in Pharmaceutical Sciences. Ensure QMS compliance in qualification and manufacturing related activities.

M.Pharm / M.Sc ; 3-5 years of relevant experience in Quality Control department, Analytical Development Lab. Good communication, technical report writing skills and E- Mail etiquette.

Syngene International is hosting a walk-in drive for Drug Metabolism and Pharmacokinetics (DMPK) positions in Bengaluru, Karnataka.

UNDERSTAND DESIGN, SETUP, AND EXECUTION OF IN VIVO PHARMACOLOGY MODELS FOR EXPERIMENTS ASSOCIATED WITH GROSS IMMUNOLOGY, SOLID TUMORS, AND HEME-ONCOLOGY

Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC