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.
Minimum Requirements
- 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.
KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.
KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.
I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.
I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.
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