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Biopharmaceutical Manufacturing Associate; Split Shift

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Astrix Technology
Contract position
Listed on 2026-06-19
Job specializations:
  • Manufacturing / Production
    Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 26 - 30 USD Hourly USD 26.00 30.00 HOUR
Job Description & How to Apply Below
Position: Biopharmaceutical Manufacturing Associate (Split Shift)

Biopharmaceutical Manufacturing Associate (Split Shift)

Science & Research

Chicago, Illinois, US

Biopharmaceutical Manufacturing Associate (Upstream/Downstream)

Location: Chicago, IL (downtown area - On-site)

Schedule: Split Shift- 1st/2nd (6am-2:30p/ 2p- 10:30pm) rotates every 2 weeks

Employment Type: 5 month Contract-to-Hire

Pay: $26-30/hr (wiggle room for more with relevant experience)

Overview

Our client, a growing biopharmaceutical manufacturing organization
, is seeking Manufacturing Associates to support production of biologic products in a cGMP-regulated environment
. This is an excellent opportunity for recent graduates (Bachelor’s or Master’s level) or early-career professionals looking to gain hands‑on experience in biotech manufacturing operations
.

Key Responsibilities
  • Perform upstream and/or downstream bioprocessing activities in a pilot plant or full-scale manufacturing environment
  • Support cell culture, fermentation, and harvest processes using bioreactors (up to 250L scale)
  • Execute purification processes including column chromatography and filtration (TFF, depth filtration, etc.)
  • Prepare media, buffers, and solutions following batch records and SOPs
  • Perform aseptic processing and fill/finish operations in cleanroom environments
  • Monitor processes using PLC/HMI systems and perform in-process testing (pH, conductivity, etc.)
  • Accurately complete batch records and cGMP documentation
  • Assist with deviations, CAPA, and change control documentation as needed
  • Troubleshoot equipment and support continuous improvement initiatives
  • Maintain cleanroom standards, safety compliance, and proper material handling procedures
Qualifications
  • Bachelor’s or Master’s degree in Biology, Biotechnology, Biochemistry, Chemistry, or related field preferred
  • 1–5 years of experience in biotech or pharmaceutical manufacturing (internships/co‑ops highly considered)
  • Hands‑on experience with cell culture and/or purification (chromatography, filtration) required
  • Exposure to cGMP environments and cleanroom operations preferred
  • Strong attention to detail with the ability to follow SOPs and batch records
  • Ability to work off‑shifts (split or overnight)

Note:

Academic‑only bench research without scale‑up/manufacturing exposure is not sufficient

Why Apply?
  • Strong opportunity for recent grads to break into biopharma manufacturing
  • Hands‑on experience with real production‑scale equipment and processes
  • Exposure to both upstream and downstream operations
  • Opportunity to convert to a long‑term, stable position

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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Position Requirements
10+ Years work experience
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