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2.0 - 6.0 years
0 Lacs
navi mumbai, maharashtra
On-site
As a Research Scientist in our company, your role involves ensuring the completion of experiments and generating accurate and reproducible data. You will be responsible for developing relevant models and validating them. Your key responsibilities will include: - Supervising and executing laboratory / pilot plant experiments related to the research area - Organizing facilities for experiments including chemicals, equipment, and analytical methods - Participating in pilot plant operations / studies and utilizing results for model development - Supporting plant operations and collecting data for relevant analysis - Uploading reports on the portal and preparing Internal Technical Reports As for ...
Posted 3 weeks ago
2.0 - 6.0 years
0 Lacs
jamnagar, gujarat
On-site
As a Research Scientist, your role involves ensuring the completion of experiments and generating accurate and reproducible data. You will be responsible for developing relevant models, validating them, and supervising laboratory/pilot plant experiments. Your key responsibilities include: - Supervising and executing laboratory/pilot plant experiments related to the research area - Organizing facilities for experiments, such as chemicals, equipment, and analytical methods - Participating in pilot plant operations and utilizing results for model development - Providing support to plant operations and conducting data analysis - Uploading reports on the portal and preparing internal technical re...
Posted 2 months ago
2.0 - 8.0 years
0 Lacs
kochi, kerala
On-site
You will be working at Silmed Scientific, an organization dedicated to public health safety through scientific evaluation and assessment of healthcare products. The company aims to ensure the global availability of safe products and fosters a unique working culture. As a Regulatory Medical Writer at Silmed Scientific, your primary responsibilities will include: - Authoring and reviewing Regulatory submission documents for pharmaceutical marketing authorization in Europe and the United States. - Developing Common Technical Document (CTD) modules like nonclinical and clinical overviews & summaries (Module 2.4, 2.5, 2.6, and 2.7), expert reports, safety & efficacy summaries, as well as Aggregat...
Posted 3 months ago
2.0 - 6.0 years
0 Lacs
vadodara, gujarat
On-site
You will be responsible for ensuring the completion of experiments and generating accurate and reproducible data. This will involve developing relevant models, validating them, and supervising laboratory/pilot plant experiments within the research area. Your duties will include sample preparation, characterization, and evaluation, as well as organizing facilities and resources for experiments. Additionally, you will participate in pilot plant operations/studies and use the results as boundary conditions for model development. Supporting plant operations, collecting data, conducting analysis, uploading reports, and preparing Internal Technical Reports are also part of your responsibilities. T...
Posted 4 months ago
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