Company Jobs

Deep understanding of Pharma GMP testing industry and the testing requirements of Method Development and Validation, Trace analysis Nitrosamine, Elemental, Genotoxic, Related substances E&L Testing & Packaging testing.

Support Formulation R&D in arranging the materials for development, optimization, confirmatory and exhibit batches which are under development in Hyderabad surround locations. API samples, Impurities, Working standards support for Formulation development stage.

Preparation of SOPs, BMRs, Protocols, Interim and Summary Reports for products, and Qualification, Re-qualification documents.

SCIENCES, PHARMACY GRADUATES B.SC, M.SC, B. PHARM, M. PHARM WITH 0 TO 3 YEARS EXPERIENCES IN ANY OF QA FUNCTION VALIDATION, IPQA, QMS, COMPLIANCE, DQA, LAB QA OF A FORMULATION - STERILE, NON STERILE DOSAGE

M.Sc. / M.Pharm, Technically competent on analytical method development and Validation of complex products like liposomes, transdermal, long acting injectable, suspensions, Nano particles, Microspheres, topicals and peptides. Responsible for developing, establishing, and validating analytical testing methodologies, transfer; ensure all analytical testing activities are in compliance with applicable regulatory guidance. 

B.Pharma / M.Pharma / M.Sc.; Experience in Quality Assurance QMS, AQA, Process Validation, IPQA, RACoordinator, Training, Computer System Validation. Macleods Pharmaceuticals Ltd. is one of the fastest growing pharmaceutical company.

B.Pharma / M.Pharma/ B.Sc / M.Sc. (Organic Chemistry / Analytical Chemistry); experience in injectable manufacturing, Aseptic area operations, Packing, Visual inspection, QMS activities. relevant functional experience in OSD manufacturing and Packing operations / QMS activities

B.Pharma, B.Sc., M.Sc.  Granulation, Compression, Coating, Continuous coater, Capsulation, Press-fit, Inspection. Blister Packing, Bottle Packing, Bulk Packing. Exhibit/IP/FP, Hold Time, Stability, Vendor Qualification, Method Validation and GLP, RM, PM, VQ, Sample Management

Manufacturing, filtration, filling, Lyophilization, sealing, and pre- and post-manufacturing activities. Planning and execution of batch manufacturing activities, filling activities, lyophilization, sealing activities, and filter integrity. Monitoring NVPC and trending.