Upstream Process Development Technician/Research Associate
at KBI Biopharma
Plan-les-Ouates, GE, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 22 Jan, 2025 | Not Specified | 23 Oct, 2024 | N/A | Good communication skills | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Job summary
The Upstream Process Development Technician/Research Associate executes laboratory studies and support Scientists within the KBI Biopharma (KBI) Upstream Process Development organization under general supervision.
Job Responsibilities
Responsibility
Approximate % of Time
Execute laboratory experiments of upstream process development including preparing solutions, running upstream unit operations (cell culture, clarification, filtration, solution preparation, etc.), and executing basic analysis of process samples (Cell count, metabolites analysis, etc.).
65%
Normally exercises judgment within defined procedures and practices to determine appropriate action (sometimes called upon to exercise judgment outside of defined procedures)
5%
Makes detailed observations about experimental deviations from the expectations and carries out elementary analysis of the data to determine data that should be rejected because of exceptional laboratory conditions.
5%
Understands experiments and conducts troubleshooting analysis.
5%
Maintains and updates knowledge of instrumentation and maintenance. Schedules periodic maintenance for laboratory equipment.
5%
Documents procedures, observations, and results in laboratory notebooks and responsible for maintaining training compliance, according to site expectation.
15%
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.
Ongoing
Able to react to change productively and handle other essential tasks as assigned.
Ongoing
Total:
100%
Minimum Requirements
Preferred Knowledge, Skills, Abilities
A.S. specifically in Biotechnology or associated field, or B.S. degree in biology, biochemistry, chemistry, engineering, or related area (with equivalent training). Experience in various stirred tank reactors (single-use or stainless) is highly preferred.
Energetic, motivated, and dynamic individual. Must be organized and able to focus in a multi-tasked environment and maintain operational efficiency and positive demeanor.
Must be available to perform off-hours shift and week-end work, depending on laboratory activities and organizational need.
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
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Hospital/Health Care
Pharma / Biotech / Healthcare / Medical / R&D
Health Care
Graduate
Proficient
1
Plan-les-Ouates, GE, Switzerland