walk in jobs

M.Sc / B.Pharm / M.Pharm. Material Dispensing, Ointment, Gel Manufacturing, Filling, Packing, Track and Trace, Labelling, Cartonator, QMS. IPQA, Document Cell, OOS, OOT, Process/ Cleaning Validation, Review of BMR & BPR, Training ,QMS Investigation, CAPA, SOPs etc.

Supervision of aseptic area activities, shift handling, aseptic area documentation, media fill activities, aseptic behaviour monitoring, and sterile operations. Handling area cleaning and sanitation activities, supervising steam sterilizer loads, filter integrity, disinfectant preparation and filtration activity, and related documents.

M.Pharm, B.Pharm, M.Sc, B.Sc. Functional experience in Calibration, Instrumentation, QMS activities. relevant functional experience in OSD manufacturing and Packing operations / QMS activities. Through knowledge on cGMP norms & Laboratory safety

B.Sc. / B.Pharma / B.Tech. Food; Tirupati Group is contract manufacturer of Pharmaceuticals, Nutraceuticals, Ayurveda & Sports Nutrition products.

BSC /MSC/ B.Pharm/ M.Pharm; Having experience in government tendering, CPP portal, Having exp. in MS Office & fluency in English.. Willingness to learn new things, Open for Challenges, Computer Skills, Ready to work in shift. Having experience Daily Maintenance work, knowledge of utility, Plant Maintenance, Electric and mechanical work. Having experience of handling of HPLC, GC & Documentation

B. Pharma, D. Pharma, BHMS, BAMS, BUMS, BDS, B.Sc. Life science, M.Sc. Life Science, and Diploma in Clinical Research. Preference will be given to the candidates having relevant experience in Clinical Research.

B.Sc./ B. Pharmacy /M.Sc. M. Pharmacy; Preparation and review of Standard operating procedures Retrieval of BPCRs in case of batch cancellation, planning changes. Handling and Execution and investigation of QMS documents in change controls, deviations, and CAPA.

M.Sc. / B. Pharm / M. Pharm. Review of Electronic data on various QC instrument Like HPLC, GC, FTIR, UV-Visible Spectrophotometer, TOC analyzer etc. Details experience on Audit Trail review of All QC instruments. Hands on Experience on Various QC instrument calibration like HPLC, GC, FTIR, Polarimeter, UV-Visible Spectrophotometer, Dissolution etc. Experience on Handling of OOS, OOT, OOC, Laboratory Incident investigation, Deviation etc.

Require experience in IPQA, IPQA Sterile, Qualification Sterile, Validation Sterile, Analytical QA, Stability Studies, regulatory affairs, OOS investigation Microbiological, Risk Assessment, Market Complaint, QA Documentation, Exposure in QMS, Deviation, CAPA etc with Trackwise system.