Pharmaceutical Process Engineer (C + Q)
San Jose, CA
Pharmaceutical Process Engineer (C+Q)
Our client is a biologics company operating as a multiproduct cGMP facility. They are in need of a process engineer to help with commissioning and qualification initiatives.
Day to Day Responsibilities:
The consultant will come into client as a process engineer specifically helping in the areas of commissioning and qualification. Our client operates out of a biologics manufacturing site, so this person should come from this type of background. They will also be responsible for writing reports and creating protocols, so they should have strong writing skills. Among some of the different types of equipment consist of bioreactors, single use mixers and purification equipment so it is important they also have prior hands-on experience with this.
- Process Engineer
- Commissioning & Qualification
- Creation of Protocols/Write Reports
- Bioreactors, purification equipment, etc.
Job Type: Contract