ITI

Knowledge of Dispensing in warehouse of Raw Material & Packing Material. Manage daily production QMS activities (deviations, OOS/OOT investigations, CAPA, change control) with proficiency in PowerPoint, Excel, Al tools & knowledge of manufacturing process

ITI / Diploma for Operators (Sterile USFDA Exp.) B.Pharm / M.Pharm for Officer (Sterile USFDA Exp.)

Looking for Supervisor and Operators with Injectable Aseptic Area / Terminal Sterilization Packing experience in Manufacturing.

QMS & Audit Compliance: Implementation and maintenance of QMS, document control, internal audits, audit preparation, inspection support and CAPA follow-up.

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

Candidates with knowledge of GMP, documentation, and compliance, along with Formulation experience & Regulatory exposure will be considered.

Experience in analysis of Solid Oral - FP, Instrumentation, In-process or Stability. Experience of Analytical Method Validation. Experience of PMQC & Dissolution. 

Perform line clearance. In-process venficatoon and batch reconciliation. Investigate deviations, incidents and support CAPA implementation Coordinate equipment qualification, preventive maintenance and calibration activities.

Aspiro Pharma Limited - Speciallities is a USFDA Approved plant and part of the Hetero Group, committed to delivering high-quality sterile injectables to global markets.