Ipca is a fully integrated, rapidly growing Indian pharmaceutical company with a strong thrust on export. Ipca'a API and Formulation produced at world class manufacturing facilities are approved by leading drug regulatory authorised including the USFDA.
Post : Manager - Quality Assurance (QMS & Documentation Lead)
Experience in Regulatory Affairs, CMC, Manufacturing, Quality Assurance/Control, Process Development, or Analytical Development in the pharmaceutical or biotechnology industry
M.Pharm, B.Pharm, MSc ; Environmental Monitoring activities in a sterile/aseptic manufacturing facility. Conduct and supervise non-viable particle monitoring and line clearance operations.
Exposure to OSD Manufacturing operations like Compression, Pellet coating, Capsule filling, Primary Packing & Secondary Packing. Expertise in e-BPR and e-log will be added advantage.
Analytical Method Development, Validation, Transfer activities of test like Assay, RS, Dissolution and Solvent. Calibration of the Analytical instruments like HPLC, GCHS, IR, UV & Disso as per the master calibration schedule.
Biological E. Limited invites both experienced professionals and fresh diploma holders, as well as graduates and self-driven individuals, to join its Speciality Injectables Business located in Shamirpet, Hyderabad.
Candidate should be proficient in GLP. HPLC. GC, Instrumentation. Chemical Analysis, Raw Material Analysis, FG Analysis, UV. FTIR. In-Process Sample Analysis, and Stability Sample Analysis.