Ahmedabad

Project Managers provide business and technical leadership for one or more projects within a business unit, leading project teams through the identification, justification, prioritization, initiation, development and implementation processes. This Sr. Specialist position will act as a Project Manager leading commercial launches in US and Global markets within the Pharmaceutical Business segment.

Ph.D degree in relevant field and first class or equivalent at either Bachelors or Masters level in the relevant branch. AND Minimum of 10 years of experience in teaching, research, industry out of which at least 3 years shall be at a post equivalent to that of an Associate Professor.

HPLC, GC, IR, UV, Dissolution and other QC Equipment, QC Method Validation and Transfer.

M.Pharm / MSc; Experience in Analytical Method Development of Assay, Related Substances and Dissolution method for oral solid dosage form. relevant experience with OSD products for Regulatory Market in the Analytical Department.

M.Pharm / B.Pharm / M. tech / B. tech / B.E. / B.sc / Diploma / ITI; Tablet, Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. HPLC, GC, IR, UV, Dissolution and other QC Equipment, QC Method Validation and Transfer.

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

To Perform analytical activity of Development, Scale-up support, Method validation, Method transfer, Release, Stability, Drug product characterization, E&L study, In-Vitro study, routine analysis of inhalation dosage forms. M.Pharm, MSc

M.Sc. M.Pharma. M.V.Sc. from a recognised University. Institute. 4 years of experience of research, teaching in Central State Govt. Organisations, University or Research Institution or Central. State autonomous or other recognised institute of repute; The application must be filled in online mode and the hard copy of duly filled online applications forms with required annexure must reach to NIPER-A

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.