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FIlling Supervisor
Manufacturing
chicago, IL, US
Pay Rate Low: 35 | Pay Rate High: 38
Pay Rate Low: 35 | Pay Rate High: 38
- Added - 12/11/2025
We have an opportunity for an experienced Filling Supervisor to continue their career in downstream/upstream manufacturing. This role will be with our client who has a global footprint in both R&D and manufacturing within the biopharma industry.
Pay: $35-38/hr
Schedule: 1st shift 8:30-5 Mon-Fri
Location: Chicago, Illinois
Type of Job: Temp to Hire
Responsibilities:
• Follow work instructions, production specifications, and SOPs to meet production goals and maintain quality data.
• Perform and oversee aseptic manufacturing operations, including:
• Verify and document use of raw materials, packaging materials, and consumables.
• Complete all logbooks, batch records, and cGMP documentation accurately and on time.
• Troubleshoot equipment and process issues; report nonconformances and assist with investigations and CAPAs.
• Ensure compliance with all safety, cGMP, and company policies.
• Train, coach, and supervise team members in cleanroom operations, SOPs, and regulatory compliance.
• Review, approve, and update manufacturing documentation to align with regulatory requirements.
• Support process improvement initiatives, technology transfer, and validation activities.
Requirements:
• Education:
We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
INDBH
#LI-DNP
Pay: $35-38/hr
Schedule: 1st shift 8:30-5 Mon-Fri
Location: Chicago, Illinois
Type of Job: Temp to Hire
Responsibilities:
• Follow work instructions, production specifications, and SOPs to meet production goals and maintain quality data.
• Perform and oversee aseptic manufacturing operations, including:
- Line inspections and line clearance of ISO6, ISO7, and ISO8 areas.
- Weighing, dispensing, formulation, and filtration of drug products.
- Operating equipment such as autoclaves, part washers, syringe fillers, and peristaltic pumps.
- Performing pH/conductivity calibration, filter integrity testing, and non-viable particle counts.
• Verify and document use of raw materials, packaging materials, and consumables.
• Complete all logbooks, batch records, and cGMP documentation accurately and on time.
• Troubleshoot equipment and process issues; report nonconformances and assist with investigations and CAPAs.
• Ensure compliance with all safety, cGMP, and company policies.
• Train, coach, and supervise team members in cleanroom operations, SOPs, and regulatory compliance.
• Review, approve, and update manufacturing documentation to align with regulatory requirements.
• Support process improvement initiatives, technology transfer, and validation activities.
Requirements:
• Education:
- Bachelor’s degree highly preferred (or equivalent 6–8 years of relevant industry experience).
- Minimum 1 year in a supervisory or lead role
- Experience with aseptic techniques and cleanroom manufacturing strongly preferred.
- Prior experience in GMP/biotechnology operations (formulation, filtration, aseptic sampling, etc.).
- Strong knowledge of GMP, aseptic practices, and safety regulations.
- Ability to operate and troubleshoot complex manufacturing systems and equipment.
- Proficient with computer systems such as POMS, LIMS, SAP, or NetSuite.
- Strong written and verbal communication skills; able to understand and follow technical documentation.
- Excellent interpersonal and leadership skills with the ability to train and mentor others.
- Sound problem-solving and decision-making abilities.
We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
INDBH
#LI-DNP
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FIlling Supervisor