Analytical method validation of different methodology. Dissolution Method Development and validation. Validation and method development protocol and report preparation.
Stallion Laboratories incorporated in 1988 as an integrated private sector Pharmaceutical Formulation Manufacturer, has acquired an unmatched record of managing niche product in formulations with a WHO GMP approved production facility and GLP qualified stringent quality control.
Formulation development of Injectable including development, execution, filing and approval of Complex Injectables viz. Liposomes, Peptides, long acting emulsions, suspensions, in-situ gels, Lyophilised injectable etc.
areas of life science/ medical device/pharmaceuticals/ engineering / science; Experience in the area of orthopedic, neurological, ocular implants or Biosensors or IVDs or therapeutic devices Drug-device combinations with proven track record through published high-impact research papers, patents and product development.
PhD or MBA, PGDM or PMP certification with any science, engineering, management bachelor degree with 3 years of experience in startup incubators or MSc, MTech, MS, M.Pharm, ME with at least 5 years of experience in startup incubators.
Functionalized s-Heptazine containing materials and their Applications in CO2 Utilization. The main objective of this project is to construct s-Heptazine based systems and their functionalization metal-free and metallated systems for their applications as heterogeneous catalyst in the utilization of CO2 for various value added products like cyclic carbonates, polycarbonates and so on.
2-8 years into receipt & dispensing activity, inward & outward activity. 2 to 8 years of experience into API / Intermediates Manufacturing. 2-5 years of experience in Granulation, Coating, Compression, Blister Secondary and Cartonator, Bulk Secondary
Operation and Calibration of HPLC Waters and SHIMADZU, GC, UV, FTIR, K, F, MS, IC and other instruments, Instrument Qualification knowledge required. Analysis of Raw material and Excipients and handling of HPLC Waters and SHIMADZU, GC Agilent, UV, FTIR, K/F, AAS, 1C and other instruments
M.Sc. Biotechnology, Microbiology or relevant life sciences discipline with a minimum of 55% marks. Minimum experience of two years as researcher. Establishment of synthetic antibody engineering platform for rapid development of indigenous bispecific antibodies to debilitate zoonotic pathogens reducing their pandemic potential.
M.Pharm, MS Pharm, MSc or Equivalent with specialization in Biotechnology, Microbiology or Life sciences. Investigating of the role of LncRNA PANDAR in the progression and metastasis of ovarian cancer. Prior experience in basic techniques in Molecular Biology, Cell culture and Biochemistry are desirable but not mandatory.