Astrix
Biopharmaceutical Manufacturing Associate
The Manufacturing Associate supports the production of biotechnology products for clinical and commercial use. This role involves working in controlled cleanroom environments using aseptic techniques while adhering to cGMP, SOPs, and all regulatory requirements.
Pay : $30-$36/hr, depending on experience
Shift : Rotating 1st/2nd shift, and a 3rd shift available
Key Responsibilities
Perform manufacturing operations such as material weighing, media/buffer preparation, filtration (TFF, depth, dead‑end), fermentation, harvest, chromatography, and aseptic final filtration.
Operate and monitor process equipment and control systems (PLC, HMI) and perform in‑process testing (pH, conductivity, spectroscopy).
Accurately complete batch records, logs, and other GMP documentation.
Maintain inventory, verify raw materials, and perform data entry in MES.
Ensure cleanliness of equipment and cleanroom areas per established schedules.
Handle and dispose of hazardous materials in accordance with EHS standards.
Troubleshoot equipment and process issues; train and guide peers as needed.
Support technology transfer and continuous improvement initiatives.
Report deviations, nonconformances, or equipment issues promptly.
Qualifications
Associate degree in Biology, Chemistry, Biotechnology, or related field; or 2–4 years of relevant industry experience.
Experience with aseptic techniques and cleanroom manufacturing preferred.
Ability to follow SOPs, operate complex systems, and troubleshoot processes with minimal supervision.
Strong communication, teamwork, and documentation skills.
Proficiency with computer systems (e.g., MES, SAP, LIMS) and Microsoft Office.
Seniority Level Associate
Employment Type Full-time
Job Function Manufacturing and Science
Benefits Medical insurance
Vision insurance
Greater Chicago Area
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Pay : $30-$36/hr, depending on experience
Shift : Rotating 1st/2nd shift, and a 3rd shift available
Key Responsibilities
Perform manufacturing operations such as material weighing, media/buffer preparation, filtration (TFF, depth, dead‑end), fermentation, harvest, chromatography, and aseptic final filtration.
Operate and monitor process equipment and control systems (PLC, HMI) and perform in‑process testing (pH, conductivity, spectroscopy).
Accurately complete batch records, logs, and other GMP documentation.
Maintain inventory, verify raw materials, and perform data entry in MES.
Ensure cleanliness of equipment and cleanroom areas per established schedules.
Handle and dispose of hazardous materials in accordance with EHS standards.
Troubleshoot equipment and process issues; train and guide peers as needed.
Support technology transfer and continuous improvement initiatives.
Report deviations, nonconformances, or equipment issues promptly.
Qualifications
Associate degree in Biology, Chemistry, Biotechnology, or related field; or 2–4 years of relevant industry experience.
Experience with aseptic techniques and cleanroom manufacturing preferred.
Ability to follow SOPs, operate complex systems, and troubleshoot processes with minimal supervision.
Strong communication, teamwork, and documentation skills.
Proficiency with computer systems (e.g., MES, SAP, LIMS) and Microsoft Office.
Seniority Level Associate
Employment Type Full-time
Job Function Manufacturing and Science
Benefits Medical insurance
Vision insurance
Greater Chicago Area
#J-18808-Ljbffr