This position would sit in Alachua, FL (100% on-site)
Please note, this will be a hands-on role, looking for either Process, Industrial, or Quality Engineers to join the team for a long term contract, 1+ years (upwards of 2+).
This is the most recent addition to the requirements they are looking for in this role, particularly upstream/downstream experience in Biotechnology. If you have anyone with strong experience in the following, please send over.
Experience with Biotechnology equipment
Experience in upstream and downstream processing of biologics/vaccines
Experience with modalities including monoclonal antibodies, viral vaccines, gene therapies
Writing SOPs, CAPA, and deviation/investigation experience
- Years’ experience: 2+
- 100% on-site
- Start: ASAP
Top requirements:
- GMP experience
- Downstream activities
- Hardware/Equipment related hands on experience
- Biotech Industry
- *CAPA Investigation*