Gujarat

Project entitled Exploring the potential of algal nutrients for cell growth and understanding its mechanism at a molecular level. M.Sc Biotechnology, Microbiology or relevant life sciences discipline with a minimum of 55% marks.

Preparation and review of test procedure, development reports, method validation protocol and LNBs. Perform calibration of the analytical instruments as per calibration schedule. Analytical method development, validation, and sample analysis for Extractables and Leachables using HPLC, LCMS, GCMS and ICPMS. Identification and characterization of unknown impurities by LCMS.

B.Sc. / B.Pharm/ M.Sc.; Hands-on experience in Analytical Method Validation, Method Transfer, Protocol Review, Analysis of CU, BU, Assay on HPLC & UV Spectrophotometer, BD, TD, PSD & Water Content, Tests are performed daily to daily on job.

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

Pharmacist degree from a recognized institution, registration with Gujarat Pharmacist Council is required.

Conduct high-quality research in molecular biology and industrial biotechnology. Design and execute experiments, analyze data, and interpret results. Collaborate with a multidisciplinary team of scientists and researchers.

Monitor Global and Europe and Canadian markets for new product opportunities in both branded and Generic space In depth understanding of new product selection processes including portfolio management Primary responsibilities for executing out-licensing activities for the companies approved and In-development projects including financial modelling

01 to 05 with relevant functional experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities

Quality Management System oversight and implementation, Validation processes for production systems, In-Process Quality Assurance for General Injectable and Oral Solid Dosage forms.

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.