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Document Control Specialist

Job in Chicago, Cook County, Illinois, 60684, USA
Listing for: Astrix Technology
Seasonal/Temporary position
Listed on 2026-07-08
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers, Production QC/QA, QA Specialist - Analyst/Manager
Job Description & How to Apply Below
** Document Control Specialist*
* Existing

Chicago, Illinois, US

+ Added - 04/07/2026

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:

** 1 st 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 1 st  shift or 2 nd  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_*
* 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.
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