4-5

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.

B.Pharm/ M.Pharm / M.Sc; Hiring for SEZ 1 OSD Manufacturing Unit, Ahmedabad. IPQA / equipment qualification /QA QMS; Granulation, IGL, Compression, Coating, Wurster coating, Capsule filling

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

Formulation development in solid orals tablets, Capsules, Pellets, Soft gels. Should have experience in extended release, delayed release, multiparticulate.

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.

M. Pharma / B. Pharma; Awareness of regulatory requirement, ANDA filing & new Product filing application, Handle Field Alert Report, Market complaint, Review & presentation of Data, Tracking of data. Planning for sample pullout, Batch charging, storage & reconciliation, destruction & smooth functioning of Stability chamber, Walk-in Chamber