Management Trainee - Project Engineer Indiano Chrome Private Limited

3.0 - 7.0 years

0 Lacs

khordha

On-site

You will be responsible for project documentation and preparing project status reports by collecting, analysing, and summarizing information from various plants. You will need to coordinate and follow-up on PO Deliveries & Approvals, review reports, and project plan execution. Your role will involve ensuring Project Execution as per guidelines & PO/Contract terms, site monitoring for ongoing projects completions, preparation of work progress reports, and reporting to the project head/management to ensure the projects" overall direction and integrity. You will also determine project specifications by studying drawings layouts/product design, customer requirements, and performance standards, a...

Posted 1 month ago

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MRM Support & ChartBook, Global Investment Office, Associate, Wealth Management Morgan Stanley

3.0 - 7.0 years

0 Lacs

maharashtra

On-site

Role Overview: You will be based out of Mumbai, working across multiple teams in the Global Investment Office (GIO) at Morgan Stanley. Your primary responsibility will be to audit quantitative models to ensure their compliance with the Model Risk Management (MRM) group's requirements. Additionally, you will conduct model testing, provide written summaries of findings, and support performance dashboards within GIO for data-driven decision-making. Key Responsibilities: - Conduct model validation by challenging assumptions, mathematical formulations, and implementations. - Independently test models for accuracy and robustness under various scenarios and market conditions. - Write comprehensive ...

Posted 1 month ago

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Senior Associate Endo

3.0 - 7.0 years

0 Lacs

indore, madhya pradesh

On-site

As a Quality Control Analyst, your primary responsibility will be to review various analytical documents related to raw materials, packing materials, in-process materials, hold time, finished products, stability studies, analytical method validation/verification protocols, reports, and raw data. You will also be involved in the review and approval of specifications for API, excipients, packing materials, in-process materials, finished products, and stability studies. Additionally, you will be tasked with reviewing qualification documents (IQ/OQ/PQ) of equipment and instruments, as well as investigating and reviewing reports of laboratory Out of Specification (OOS) results, Out of Trend (OOT)...

Posted 3 months ago

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