What are the responsibilities and job description for the Biopharmaceutical Manufacturing Associate (Upstream/Downstream) position at Astrix?
Pay Rate Low: 25 | Pay Rate High: 35
Biopharmaceutical Manufacturing Associate (Upstream/Downstream)
Location: Chicago, IL (On-site)
Schedule: 3rd Shift: 10:00pm–6:30am
Employment Type: 5 month Contract-to-Hire
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
Biopharmaceutical Manufacturing Associate (Upstream/Downstream)
Location: Chicago, IL (On-site)
Schedule: 3rd Shift: 10:00pm–6:30am
Employment Type: 5 month Contract-to-Hire
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
- 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)
- 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