3rd Shift Set-Up Technician — Medical Fill & Sterilization

Fresenius Kabi USA, LLC; Grandyle Village (NY); On-site; USD 18,000 - 29,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401K with company contribution

Wellness program

Job summary

Fresenius Kabi USA, LLC is seeking a Set-up Operator for the 3rd shift (10:00 PM–6:30 AM, Monday–Friday) in our sterile filling environment. The role involves cleaning, visual inspection and assembly of filling room equipment, and operating component sterilization equipment.

A High School diploma or GED is required; mechanical aptitude or assembly experience is preferred. Good communication and documentation skills are essential, and prior experience in a cGMP production environment is a plus.

Qualifications

• High School diploma or GED required.
• Mechanical aptitude and/or assembly experience preferred.
• Must comprehend math, reading and basic mechanical adjustments.
• Good communication and documentation skills required.
• Medical, food, or other cGMP production environment experience preferred.
• Adhere to and stay current on all training requirements.
• Wear clean room safety equipment/apparel and maintain safe work environment.

Responsibilities

• Set-up Operators clean, visually inspect and assemble filling room equipment.
• Operate component sterilization equipment in sterile product manufacturing environments.
• Work the 3rd shift from 10:00 PM to 6:30 AM, Monday through Friday nights.

Skills

Mechanical aptitude

Assembly experience

Math skills

Documentation skills

Education

High School diploma or GED

Job description

Fresenius Kabi USA, LLC is seeking a Set-up Operator for the 3rd shift (10:00 PM–6:30 AM, Monday–Friday) in our sterile filling environment. The role involves cleaning, visual inspection and assembly of filling room equipment, and operating component sterilization equipment.

A High School diploma or GED is required; mechanical aptitude or assembly experience is preferred. Good communication and documentation skills are essential, and prior experience in a cGMP production environment is a plus.