• FIlling Supervisor

    Astrix Technology (Chicago, IL)


    FIlling Supervisor

     

    Manufacturing

     

    chicago, IL, US

    Pay Rate Low: 35 | Pay Rate High: 38

    + Added - 12/11/2025

     

    Apply for Job

     

    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:** 1 st 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.

    • Maintain cleanroom conditions through regular cleaning and sanitization per SOPs.

    • 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).

    • 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.).

    • Skills:

    + 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

    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.