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
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.
Sciences or Pharmacy Graduates with o to 5 years Experiences in parenteral manufacturing vial, ampoules, bottles of glass or Plastic through, BFS technology, Bag Line.
Candidate should have Exposure of Fette, Sejong, Legacy, Korsch, Cadmach or any other machine having Automatic Weight Control , Compaction Force Control, Handling of QMS Work
Have good knowledge in Granulation area Handling ACGTop spray granulation Machine, Compression area exposure for Handling Cadmach 45 station AWC Machine, Coating area exposure for Handling ACG coating Machine, Capsule filling exposure for Handling AF 25 machine.
Seeking an HPLC Analyst skilled in the operation and troubleshootingof HPLC systems, with expertise in analyzing in-process, intermediate, raw material, packaging material, finished product, and stability samples, as well as proficiency in handling GC, IR, UV-Vis, KFTitrator,AutoTitrator,SOR,and wet lab techniques