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Research associate (analytical development and quality control)

Châteauneuf
KBI Biopharma
EUR 80’000 pro Jahr
Inserat online seit: 11 Juli
Beschreibung

The research associate will be trained to execute analytical test methods and their corresponding analytical techniques. The research associate will be engaged in executing experimental protocols and performing data analysis in AFS laboratories. It is expected that the analyst will spend up to 70% of their time in the laboratory activities. The work will explore to both GMP and non-GMP analysis and associated work procedures.

Job Responsibilities

* Engage in the development of analytical methods for bioanalytical techniques such as (but not limited to) HPLC, CE, icIEF, ELISA.
* Performs testing on drug substance / drug product using bioanalytical techniques such as (but not limited to) HPLC, CE, icIEF, ELISA, UV-Vis, and simple compendial testing. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals.
* Makes detailed observations and carries out elementary data analysis. Documentation (i.e. Notebook and Worksheet) upkeep and writing skills.
* Understand experiments, conducts troubleshooting analysis, and maintains knowledge of instrumentation. Assures proper labeling, handling, and storage of all chemicals used in the area, assures proper labeling and disposition of hazardous waste in satellite area; adheres to all safety requirements and follows safety procedures, and attends all required safety and health training, including handling hazardous waste.
* Able to react to change productively and handle other essential tasks as assigned.
* Completion of a B.S. degree in science, biotechnology / life science or pharmacy major with 0-1 years of experience, or Completion of a M.S. degree in science, biotechnology / life science or pharmacy major with 0-6 months of experience in similar job or in regular use of analytical methods.
* Must know the operating principles and be proficient with the operational techniques of laboratory analytical instruments.
* General knowledge of cGMP and GLP practices.
* Knowledge and appreciation for EHSS functions and processes
* Possess good oral and written communication skills in English (French will be a plus)
* Collaborative mindset with clear intention for continuous improvement.

Associate Quality • les, Plan, Switzerland

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