1 - 10 of 31 Glp Jobs

Roles and Responsivities Responsible to ensure planning and maintain high Quality standards in routine analysis. 1. To verify GLP requirement in laboratory. 2. Responsible for FDA related activiti ... view more

We are looking for competent, dynamic and motivated candidates for suitable positions for Injectable unit for our SEZ Matoda Plant. INJECTABLE REQUIREMENT 1. Sterile Manufacturing (Injectable/Paren ... view more

Check all SOPs of QC available Check the record of cleanliness of the area. Check the list of instrument/equipment update Check that activities like sampling, testing and handling of special chemical ... view more

Regulatory Document Specialist

BASIC FUNCTIONS: Responsible for the quality and regulatory compliance of Principal Investigator (PI) credentials and Essential Documents (ED) during the start-up period of the study. Work with inte ... view more

Roles and Responsibilities Development/Improvement of the assigned products and overall review of development activities. To finalize route based on literature or. feasibility of process or avail ... view more

To act as Bio-Analyst/LCMS/MS Operator. Method Development, Method Validation for the Bioanalytical complex molecules. Operation of LCMS/MS and Clinical Study sample Analysis . Analytical Instru ... view more

Quality Control analysis : To plan and provide the analysis support as per approved specification & test procedure and standard operating procedures. To maintain and manage the quality contro ... view more

Responsible for routine operation of QC Laboratory. Daily work allocation, ensuring daily reports of analyst. Technical support for analyst for instrument operation Communication with production ... view more

Roles and Responsibilities Role Purpose Product Control: Ensuring production schedules are followed and to ensure all batches achieve safety, quality & production goals Production supervision: m ... view more

AQA Preparation of Process Validation Report, Hold Time Study Report, Cleaning verification / validation protocol. Issuance, Tracking of all QMS records. QMR compilation. New product checklist ini ... view more

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