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Biopharmaceutical Manufacturing Associate; Split Shift

Job in Chicago, Cook County, Illinois, 60290, USA
Listing for: Astrix Inc
Contract position
Listed on 2026-06-13
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)
Pay Rate Low: 26 | Pay Rate High: 30

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
(

Note:

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

• 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)

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

INDBH
Position Requirements
10+ Years work experience
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