Officer-Production-Dahej
Manufacturing Having Knowledge of Good Manufacturing practice in API Plants. Knowledge of Equipment Cleaning. Having knowledge of Reactor, Vacuum Pump, Distillation and All other parameter related to
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Manufacturing Having Knowledge of Good Manufacturing practice in API Plants. Knowledge of Equipment Cleaning. Having knowledge of Reactor, Vacuum Pump, Distillation and All other parameter related to
Manufacturing Having Knowledge of Good Manufacturing practice in API Plants. Knowledge of Equipment Cleaning. Having knowledge of Reactor, Vacuum Pump, Distillation and All other parameter related to
Male candidate is required to handle the complex manufacturing skid operation. Should have hands on experience for manufacturing of aqueous and emulsion types of products. Should have knowledge relate
Finished Product: - Approved COA, electronic data review checklist, raw data, worksheet, working standards/reference standards details, instruments calibration status, acceptance criteria as per speci
Water Analysis Routine water sampling. Environmental Monitoring activity and transfer release. Media preparation. Swab, Analysis. Daily documentation & related documentation. Finish Sample Analysis (
To Support in Development of Clinical Trial Protocol Review of published literature Review of pre-clinical & BA/BE reports Preparation of drat protocol Co-ordinate review of protocol with Medical Serv
Must have knowledge of safety Must have knowledge of Hazop Must have knowledge of compliance, liasioning Must have knowledge of Environment,Health and Safety
Operation, Maintenance &Maintaining Record Log Ozone System, Multi grade Check the chemical solution as per SOP
Software Development Experience in developing medium to large ASP.NET based projects Understanding and working knowledge of ASP.NET framework(s), c#, vb.net and Microsoft SQL Database Query/Store Proc
Method developments and validation of analytical method on said sophisticated instruments like HPLC , Gas chromatograph UV Spectrophotometry , autititratour , dissolution etc. as per ICH / Pharmacopei
QMS documents initiation and review: QMS documents initiation for QC. Responsibilities SOP preparation, review and tracking till closing the CCF. Initiation of Change control for departmental activity
Parenteral, Sterile Product, Manufacturing Parenteral, Sterile Product, Manufacturing Parenteral, Sterile Product, Manufacturing
Product Management promotional materials design Product Luanch Coordination with stackholders Product Sales Plan.
Knowledge of IT Hardware/Network/Software Application components Sound knowledge of Data backup technologies & SQL Database Sound knowledge of Audit trail review of instrument/Equipment/Computerized s
To ensure 21 CFR Part 11 Compliance in Manufacturing and QC of Troikaa Pharmaceuticals Ltd. To perform and evaluate the adequacy of Computerized System Validation across all sites of Troikaa Pharmaceu
Handling of overall IPQA activities LINE CLEARANCE & IN-PROCESS ACTIVITY: Line clearance in Injectable manufacturing, packing & warehouse dept. To verified the documents of area cleaning, equipment cl
Liquid Inhalation manufacturing vial filling washing Liquid manufacutring and cleaning GMP GMR document filling capa
S.N. SOP SOP Name Sub-SOP Frequency 1 Admin Employee entry & exit mamagement Biometric Daily check the process of the mobile & bag submission Dress code Frisking process Other plants/HO employees' ent
Technical Supervisor - Manufacturing operator requirement for parenteral production department (ITI persons available)
Responsible for FP/IP/Stability section activity Timely execution of Receipt , Analysis and release of FP/IP/Stability samples. Timely execution of Work allocation,Analytical data review,QMS activity
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