Packaging

Have good exposure in Plant Maintenance & Instrumentation related work in sterile facility. Have good exposure in Sterile IPQA & Sterile Qualification Related activity.

Expertise in designing, executing, and reviewing cleaning validation protocols. ensuring compliance with cGMP. EMA. and other global regulatory requirements. Specializing in stability studies, regulatory compliance, and quality assurance oversight. Managing stability programs in alignment with ICH guidelines

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world.

Production and Packing planning, Monitoring and reporting daily Production Activities, Master Creation In Pharma Cloud, SAP. IPQA, Document Issuance & Control, CSV, Stability, Validation

M.Pharm, B.Pharm, M.Sc, Handle QC instruments like HPLC, LCMS, GC,UV- spectrophotometer, dissolution apparatus, KF, IPC-OES, IR spectrophotometer. Handle QMS activities and maintain lab records.

Responsible to handle the team to achieve the set targets & maintain qualitative, quantitative as well as cGMP aspects.

Analyst Finished, Stability Section, knowledge of Instrument - HPLC, GC. Preferably know-how of Chromele on Software. Require good exposure in Lab QA related work. D.Pharma / B.Pharma / M.Pharma 

M.Sc / B.Pharm / M.Pharm; Computerized System Validation CSV, MES, Equipment Qualification; RM/PM, Dispensing, Inspection

M.Pharm / B.Pharm / M. tech / B. tech / B.E. / B.sc / Diploma / ITI; Tablet, Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater. HPLC, GC, IR, UV, Dissolution and other QC Equipment, QC Method Validation and Transfer.