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3.0 - 7.0 years

0 Lacs

karnataka

On-site

As a Senior Executive Flight Operations (IOCC) at our company, your primary responsibility is to support flight operations by performing flight dispatch and OCC duties to ensure safe, compliant, and timely flight execution. You will actively monitor, coordinate, and document all flight-related activities, support emergency response, and ensure safety compliance. - Assist flight dispatchers and operating crew in pre-flight preparation, documentation, and briefing. - Compile flight planning data such as NOTAMs, weather, fuel, routes, and RTOW charts. - File and revise ATC flight plans, obtain required clearances, and provide timely updates to the crew in-flight. - Coordinate with MCC for MEL c...

Posted 1 week ago

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12.0 - 16.0 years

0 Lacs

andhra pradesh

On-site

As Senior Manager - Process at the company located in Krishnapatnam, Andhra Pradesh, India, your role involves overall responsibility for production and planning. Your main accountabilities include: - Overall responsible for Production planning and Scheduling, Material balance of Oil, chemicals, by-products, and keeping Variable cost within approved budgeted levels - Coordinate with commercial & purchase department for arranging the oils, chemicals, spare parts necessary for production - Coordinate with commercial & purchase department for dispatches of co-products, by-products, hazardous waste necessary for smooth operation - Coordinate with engineering dept to implement Preventive Maintena...

Posted 4 weeks ago

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10.0 - 14.0 years

0 Lacs

dewas, madhya pradesh

On-site

You will be joining Sun Pharmaceutical Industries Ltd as a QA Sterile Manager in the Quality Assurance department. Your role will involve managing the Quality Assurance functions of the Manufacturing Block P. As the Manager-I, you are required to hold an M.Sc. degree in Biotechnology, Microbiology, or Chemistry with over 10 years of experience in the field. Your responsibilities will include ensuring that manufacturing and packing processes are carried out per SOPs and cGMP regulations. You will be responsible for certifying batch production records, releasing/rejecting batches after thorough reviews, and tracking the QMS system. It will be your duty to investigate complaints, deviations, OO...

Posted 3 months ago

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