Ahmedabad

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.

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. 

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

Analysts to join our Bioanalytical Lab. The role involves conducting bioanalytical testing using LC-MS, MS, method development, method validation and sample analysis. Strong analytical skills, problem-solving abilities, and knowledge of bioanalytical tools are essential. Perform bioanalytical testing for large molecules, including monoclonal antibodies, proteins, and peptides, using immunoassays such as ELISA, MSD, and ligand-binding assays.

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.

Perform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc. Preparation of method validation/verification protocol.

Patent search, literature search, Pre formulation study, Formulation optimization with QBD approach. Scale up at plant level.