Job opportunity
Aseptic Filling Operator AbbVie
AbbVie
Apply aseptic filling and documentation skills as a Filling Operator supporting AbbVie’s Unit Dose department. Work within a Grade B environment.
The Filling Operator performs tasks supporting aseptic product filling in AbbVie’s UD Filling department. Responsibilities include in-process quality control checks, machine checks, and monitoring punching activities. The role also includes documentation, janitorial backup, and adherence to aseptic practices.
Key Responsibilities:
Perform in-process quality control checks of Unit Dose products
Complete routine checks of Unit Dose filling machines
Monitor punching activities during batch filling
Provide backup janitorial activities
Complete documentation according to good documentation standards
Requirements:
Two to three years of pharmaceutical environment experience
Manufacturing or cleanroom experience preferred
Good computer skills
Good communication skills
Ability to follow good aseptic practices
Support AbbVie’s aseptic Unit Dose filling operations through quality checks, machine monitoring, documentation, and cleanroom practices.
#J-18808-Ljbffr
Apply on source site The Filling Operator performs tasks supporting aseptic product filling in AbbVie’s UD Filling department. Responsibilities include in-process quality control checks, machine checks, and monitoring punching activities. The role also includes documentation, janitorial backup, and adherence to aseptic practices.
Key Responsibilities:
Perform in-process quality control checks of Unit Dose products
Complete routine checks of Unit Dose filling machines
Monitor punching activities during batch filling
Provide backup janitorial activities
Complete documentation according to good documentation standards
Requirements:
Two to three years of pharmaceutical environment experience
Manufacturing or cleanroom experience preferred
Good computer skills
Good communication skills
Ability to follow good aseptic practices
Support AbbVie’s aseptic Unit Dose filling operations through quality checks, machine monitoring, documentation, and cleanroom practices.
#J-18808-Ljbffr