Associate fermentation (100%)
at LimmaTech Biologics AG
8952 Schlieren, ZH, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 13 Sep, 2024 | Not Specified | 15 Jun, 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:
LimmaTech Biologics AG is a Swiss clinical stage biopharmaceutical company. We are advancing our proprietary vaccine pipeline to halt the increasing threat of global infections due to emerging antimicrobial resistance (AMR) and sexually transmitted diseases. Working at LimmaTech is a unique chance to be part of the development of life saving vaccines.
Are you excited about the opportunity to contribute to the development of early-stage vaccines by running various biological fermentation systems using your technical and scientific skills? Would you like to be part of a team developing scalable and GMP compatible manufacturing processes to produce live saving vaccines?
To support our Upstream Process Development team, we are currently looking for an:
Responsibilities:
- Preparation, completion and documentation of USP operations
- Independent analysis of generated material (e.g. growth characteristics, productivity, etc.) with in-house methods fit for purpose
- Developing and performing robust and scalable microbial upstream fermentation processes using high-end machinery such as multi scale bioreactors and micro-, depth- and tangential flow filtration systems under guidance of an experienced supervisor
- Establishing and executing experimental strategies according to preestablished plans, timelines, and priorities
- Exploring expression systems and critical process parameters to identify optimal conditions for the manufacturing of novel products, to ensure safety and robustness for later GMP production as well as material supply for preclinical research testing
- Supporting evaluating, interpreting, and reporting of experimental data in scientific meetings and technical reports
- Maintaining and cleaning laboratory and equipment to ensure safety and operational standard
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
IT Software - Application Programming / Maintenance
Technician
Graduate
Proficient
1
8952 Schlieren, ZH, Switzerland