Packaging Associate
Astrix Technology, Chicago, IL, United States
Packaging Associate
Manufacturing
Chicago, Illinois, US
Pay Rate Low: 25 | Pay Rate High: 32
Schedule
6:00 AM — 2:30 PM
2:00 PM — 10:30 PM
Our client is hiring a
Packaging Associate
to support biotechnology manufacturing operations in
Chicago, IL . This is a hands‑on role in a highly regulated environment, offering strong pay and growth potential for candidates with GMP experience.
What You’ll Do
Perform line clearance and inspections in packaging areas
Set up and operate labeling, blister packaging, check weighers, serialization/aggregation, and tamper‑evident equipment
Complete batch records and cGMP documentation accurately and on time
Calibrate equipment, conduct in‑process checks, and troubleshoot issues
Maintain strict adherence to SOPs, cGMP, FDA, and safety standards
What We’re Looking For
GMP experience required (pharma strongly preferred)
Ability to work independently with minimal supervision
Strong documentation and computer skills (ERP/LIMS systems a plus)
Detail‑oriented with a continuous improvement mindset
This is an excellent opportunity to join a regulated biotech environment where quality and compliance are critical. If you have GMP experience and want to advance your career in manufacturing, apply today.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
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Chicago, Illinois, US
Pay Rate Low: 25 | Pay Rate High: 32
Schedule
6:00 AM — 2:30 PM
2:00 PM — 10:30 PM
Our client is hiring a
Packaging Associate
to support biotechnology manufacturing operations in
Chicago, IL . This is a hands‑on role in a highly regulated environment, offering strong pay and growth potential for candidates with GMP experience.
What You’ll Do
Perform line clearance and inspections in packaging areas
Set up and operate labeling, blister packaging, check weighers, serialization/aggregation, and tamper‑evident equipment
Complete batch records and cGMP documentation accurately and on time
Calibrate equipment, conduct in‑process checks, and troubleshoot issues
Maintain strict adherence to SOPs, cGMP, FDA, and safety standards
What We’re Looking For
GMP experience required (pharma strongly preferred)
Ability to work independently with minimal supervision
Strong documentation and computer skills (ERP/LIMS systems a plus)
Detail‑oriented with a continuous improvement mindset
This is an excellent opportunity to join a regulated biotech environment where quality and compliance are critical. If you have GMP experience and want to advance your career in manufacturing, apply today.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.
#J-18808-Ljbffr