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Manufacturing Associate

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Global Life Science Hub
Full Time position
Listed on 2025-12-01
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Manufacturing Production
Salary/Wage Range or Industry Benchmark: 26 - 40 USD Hourly USD 26.00 40.00 HOUR
Job Description & How to Apply Below

Global Life Science Hub is excited to collaborate with an innovative biopharmaceutical company leading advancements in cutting‑edge drug delivery technologies. Following two recent FDA approvals, they are gearing up for substantial growth. By 2026, they will launch new internal manufacturing facilities that will triple their production capacity, driving a significant operational expansion.

To support this next phase, we are recruiting 6 Manufacturing Associates at multiple experience levels to help meet the increasing demands of DS and DP manufacturing.

Positions Available
  • Manufacturing Associate I:
    Minimum of 1 year of experience in the biopharma sector.
  • Manufacturing Associate II
    : 2‑4 years of experience in biopharma manufacturing.
  • Manufacturing Associate III
    : 5+ years in biopharma manufacturing.
Position Information
  • Location
    :
    City of Chicago
  • Compensation
    : $26–40/hr, with relocation support for non‑local hires
  • Shift Pattern
    :
    Monday – Friday: 1st, 2nd and 3rd Shift
Key Responsibilities
  • Weighing and dispensing materials
  • Operating filtration systems
  • Inoculating mammalian or cytokine cell cultures
  • Conducting fermentation and harvest processes
  • Managing chromatography columns and TFF procedures
  • Performing in‑process tests, including pH, conductivity, spectrophotometry, osmometry, cell counts, etc.
  • Preparing media and buffer solutions
  • Completing Batch Records and other cGMP documents accurately and promptly
  • Removing and disposing of used materials from the manufacturing area
  • Ensuring that cleanroom standards are consistently met within manufacturing spaces
  • Reporting any non‑conformance or incidents to the Supervisor during shifts
  • Assisting with technology transfer from Process Development to cGMP Manufacturing
  • Adhering to safety, cGMP, and company policies and procedures
  • Carrying out additional tasks as assigned
Benefits
  • Medical insurance
  • 401(k)
  • Vision insurance
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Position Requirements
10+ Years work experience
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