Biotech Plasma Processing Technician – Night Shift

System One Clinical & Science; Los Angeles (CA); Vor Ort; USD 25.000 - 36.000; Teilzeit

Benefits dieser Stelle

Health benefits

401(k) plan

Zusammenfassung

System One Clinical & Science is seeking a Plasma Classification Associate Inspector for a night shift in Los Angeles, CA. The role requires handling setup, operation, and cleaning of processing equipment used to convert human plasma into injectable protein therapies, with strict adherence to regulatory procedures.

Responsibilities include documenting activities per FDA regulations and maintaining aseptic conditions in a clean room.

Qualifikationen

• High school diploma or GED required; Associates degree, applicable certification, and/or military veterans preferred.
• Demonstrated ability to read, write and speak English.
• Proactive, results oriented with strong attention to detail.
• Ability to prioritize and manage multiple tasks to meet deadlines.

Aufgaben

• Set up and operate equipment in a biologics processing environment.
• Follow FDA procedures and ensure compliance with regulatory requirements.
• Maintain thorough documentation in accordance with FDA standards.
• Clean and prepare facilities and equipment as required.
• Work in a clean room environment and perform basic process measurements (pH, turbidity, conductivity).
• Operate UF units, chromatography columns, CIP/SIP systems, and centrifuges.
• Utilize touch screen Operator Interface Terminals (OIT) for operations.

Kenntnisse

Attention to detail

Proactive/Results oriented

Self-starter

Prioritization

Team player

Ausbildung

High school diploma or GED

Associates degree preferred

Tools

MS Office

Jobbeschreibung

System One Clinical & Science is seeking a Plasma Classification Associate Inspector for a night shift in Los Angeles, CA. The role requires handling setup, operation, and cleaning of processing equipment used to convert human plasma into injectable protein therapies, with strict adherence to regulatory procedures.

Responsibilities include documenting activities per FDA regulations and maintaining aseptic conditions in a clean room.