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Document Control Specialist

Job

Astrix Technology Group

Chicago, IL (In Person)

$65,000 Salary, Full-Time

Posted 3 days ago (Updated 1 day ago) • Actively hiring

Expires 8/6/2026

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Job Description

Document Control Specialist Astrix Technology Group - 3.4 Chicago, IL Job Details Temp-to-hire $65,000 a year 10 hours ago Qualifications Manufacturing facility experience Bachelor's degree
Full Job Description Pay Rate Low:
65000 |
Pay Rate High:
65000 We are hiring for a Document Control Specialist who want to continue their career in biopharmaceutical manufacturing! This role will be with our client who has a global footprint in both R D and manufacturing within the biopharma industry.
Schedule:
1st shift
Location :
Chicago, Illinois Type of Job:
Temp to
Hire Responsibilities:
Provide daily administrative support to the Manufacturing Manager, including scheduling, coordination of activities, and preparation of reports Facilitate communication between Manufacturing and cross-functional departments such as Quality Assurance, Quality Control, Supply Chain, and Facilities Draft, revise, and review controlled GMP documents including Standard Operating Procedures (SOPs), batch records, and training materials Ensure document accuracy, compliance, and alignment with internal quality standards and applicable regulatory requirements Manage document routing, approval workflows, version control, and archival within the documentation management system Support Corrective and Preventive Action (CAPA) activities, including data collection, documentation, tracking, and follow up. Assist with investigations by gathering relevant data, compiling summaries, and supporting root cause analysis efforts. Provide hands-on support in cleanroom operations during periods of increased demand, staffing gaps, or special projects. Cleanroom operational support may require working 1st shift or 2nd shift.
Requirements:
Bachelor's degree in a scientific field Background in Manufacturing, Process Engineering, MSAT, Technical Services, or Quality Assurance preferred At least 2 years of related experience in a GMP manufacturing environment, pharmaceuticals or biosimilars preferred 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-LD1