Description
Essential Duties and Responsibilities include, but are not limited to, the following:- Prepares biotechnology equipment such as reactors, skids, etc for qualification studies and executes qualification/validation studies according to approved protocols and SOPs.
- Writing and executing equipment protocols and subsequent reports.
- Supporting all qualification activities - IQ/OQ.
- Ensuring GMP compliance in all activities.
- Strong background within the biotechnology or pharmaceutical industry.
- Experience working in liquid/sterile/vaccine/chemical environment.
- Proven experience working with the following equipment and processes: reactors, vessels, bulk production, harvesting, skid columns, cell culture, fermentation.
- Significant recent project based experience in the commissioning and/or qualification of pharmaceutical process equipment.
- Proactive, hands on mentality, able to hit the ground running and work independently.
- Language skills: fluent English - spoken and written.