Associate Scientist, Upstream Process Development

vor 2 Wochen

PlanlesOuates, Genf, Schweiz KBI Biopharma Vollzeit
Job summary


The Upstream Process Development Associate Scientist supports and executes laboratory studies within the KBI Biopharma (KBI) Upstream Process Development organization.

Job Responsibilities

  • Conducts laboratory experiments in support of upstream process development. This entails setup, operation, and associated analysis of mammalian cell culture processes including bioreactor preparation, autoclaving, inoculation, sampling, feeding, data entry, and data analysis for shake flask and various scale bioreactors (Ambr250, 3 L bioreactors and 200 L Xcellerex singleuse bioreactors)
  • Makes detailed observations about experimental deviations from the expectations and carries out analysis / troubleshooting of experimental data.
  • Maintains / calibrates associated equipment and instrumentation. Schedules periodic maintenance for laboratory equipment.
  • Documents operations, observations and results in laboratory notebooks (including electronic). Responsible for producing high quality documentation and client reports suitable for publication and regulatory requirements.
  • Acts as a project team member (representing US PD) for customer development programs, acting as spokesperson on associated US PD activities and interacting positively and productively with clients; Advising management on program status
  • Assures proper labeling, handling, and storage of all chemicals used in the area; assures proper labeling and disposition of hazardous waste in satellite areas; adheres to all safety requirements and follows safe 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

  • Records (accurately, clearly, and consistently) information, facts, and measurements that are required by GLP, and/or by coworkers in order to understand situations and to perform their assignments. Prepares documents using own and others' data; organizes, clarifies, and presents information for internal and external audiences using commonly available software such as MS Office.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to interpret an extensive variety of technical instructions and deal with several abstract and concrete variables
  • Understands and applies mathematical concepts and methods; interprets data and results using quantitative measures and statistical analysis; performs and documents calculations and conversions as part of standard processes; develops tests and methods to assure accuracy of processes and measures; learns and applies new quantitative concepts; performs calculations in order to diagnose or troubleshoot
  • Word processing, Spreadsheets, Power Point, Email. Experience with Unicorn, Electronic laboratory notebooks, DoE / Statistical software (i.e. JMP, Design Expert) would be an advantage
  • English required, French is a plus
Working Conditions

Flexibility of hours to support cell culture / alarm response over evenings and weekend.

  • KBI Biopharma, Inc. (KBI) is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must either (1) have provided proof of full vaccination (as defined by the CDC) with a COVID19 vaccination which has been granted FDA approval or Emergency Use Authorization; or (2) perform weekly COVID19 testing with negative test results._
  • 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._

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