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Research Associate Jobs
Company | Vantage Hemp Co. |
Address | Greeley, CO, United States |
Employment type | FULL_TIME |
Salary | |
Category | Internet Publishing |
Expires | 2023-07-10 |
Posted at | 11 months ago |
Position Summary: This is a hands-on, full-time position with duties that include playing an integral role in the research, development, and troubleshooting of large-scale production at Vantage Hemp. This position will support the research of existing and new product lines. The role is lab-based and located at our production facility in Greeley, CO.
- Maintain an up-to-date notebook.
- Aid in the research into new syntheses and processes for future considerations of new products.
- Conduct chemical reactions to further the company’s research for existing and new product lines.
- Researches, gathers data, writes, rewrites, and edits research briefs, plans, project proposals, and other written materials; and shares research information, summarizing data collection methods and research findings, with internal and external audiences.
- Assist in the development of formulations for final product lines.
- Assist with other duties as assigned.
- Report all findings in weekly meetings to the executive team.
- Conduct processes in small scale to assist the development and troubleshooting of large-scale production at Vantage Hemp. The processes may involve distillation, extraction, crystalizing, and winterization. Also, filtration and liquid chromatography.
- Bachelor’s degree in Chemistry, Chemical Engineering, or Biochemistry required.
- Master’s degree in a related scientific field preferred.
- Prior experience in extraction of CBD.
- 2+ experience in a lab conducting chemical research and/or development.
- Knowledge or experience in cannabinoid or plant-related molecule extraction and processing.
- Demonstrate scientific creativity and take the initiative.
- Well-organized working style with flexibility/adaptability to change.
- Effective oral and written communications.
- Ability to multi-task and effectively manage timelines.
- Knowledge of GMP requirements, ICH/FDA Guidelines.
- Proficient with Microsoft Office and data analysis/interpretation.
- Ability to work in a team environment but have a high level of independence for planning and executing experiments.
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