Executive - Electrical E&M - Dahej
Candidate Having Minimum 5 to 10 Years of Experience in API Pharma/Chemical Industries. Having knowledge of projects and plant maintenance. Having knowledge of DG sets, HT/LT panels, breakers, transfo
Find Pharma, Biotech, Clinical Research & Medical Jobs on Bioksha
Candidate Having Minimum 5 to 10 Years of Experience in API Pharma/Chemical Industries. Having knowledge of projects and plant maintenance. Having knowledge of DG sets, HT/LT panels, breakers, transfo
1 Hands on Working experience of Analytical Method Validation/Verification of Pharma API & Products 2 Able to prepare AMV Protocols and Reports 3 Sound Knowledge on GC / HPLC Instrumentation. 4 Able t
candidate should have min 5-15 years of industrial experience in Pharma /chemical industries in electrical departments, He should have knowledge of MCC panel, transformer, DG set, Motors etc.
Manufacturing of all products experiance with good mfg skill. Supervision of ampoule and vial filling activty with online gmp
supervision of packing and visual inspection activity . Supervison of labelling for ampoules and vial line with online GMP
Working in cGMP Pharmaceutical plant with cGMP and EHS complince. minimum 01 to 05 years exp. fully paper work with GMP complince.
Exeprince in pharmaceutical company and knowledge for Batch manufacturing self fillup. Required work with safety complience.
Sr. No. Responsibilities 1.0 Operation and maintenance related activity ; 1.1 Operation, monitoring and maintenance of Chiller, Boiler, Air-Compressor, Nitrogen Plant, HVAC System, Water System (RO-I
Required for Manufacturing and filling of paretneral products Maintian the aseptic area and monitorign the inprocess checks
Male candidate is required for operation of vial and ampoule filling and sealing machine. Should have knowledge of aseptic operation and behaviour. Should have knowledge about the parenteral productio
To fulfill the Health and Safety related Statutory and Legal requirement. To achieve goal of EHS Policy by effectively execution of its objectives. To develop EHS SOP get reviewed and implement as per
Good skill in investigation and investigation report writing. Stability management and finished product analysis planning. HPLC and other laboratory instrument knowledge. Documentation skill. Knowledg
Review of the Finished product / Raw material / stability / calibration of instrument, hands on LIMS, Investigation and documentation.
Preparation of Qualification protocol and report Review of document and compilation of document execution of qualification documents
Review of change control ,deviation, OOS and OOT documents Assign change control, deviation and CAPA to user department involve in investigation and market complain Self inspection management and plan
Analysis of Drug Product using HPLC, Particle size analyzer, Autotitrator, Chcmical testing, Documentation. Knowledge of LIMS.
Experience of documentation, calibration of instrument & equipment, LIMS, chemical testing, working standard qualification.
Legal Compliance pertaining to Environment Health and Safety Operations of ETP, STP, MEE, Laboratory and Hazardous Waste Area. GMP Documentation pertaining to EHS Department. Environmental Monitoring
Plant round to check the gaps and report to HO Report incident along with investigation and corrective and preventive action of near miss/incident/accident. Monitoring of work permit system at site an
Review of batch manuafcturing record and line clearance of area and equipment Inprocess check and sampling of bulk , finshed product AQL sampling . Packing and manufacturing sampling.
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