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Part Time Iso Document Control Jobs in Chicago, IL

Valparaiso YMCA

ACCESS CONTROL

Valparaiso, IN · On-site

$11/hr

This part-time position supports the Membership team by greeting our members as they come in and maintaining appropriate access control. OUR CULTURE: Our mission and core values are brought to life ...

Valparaiso YMCA

ACCESS CONTROL

Valparaiso, IN · On-site

$11/hr

This part-time position supports the Membership team by greeting our members as they come in and maintaining appropriate access control. OUR CULTURE: Our mission and core values are brought to life ...

ATIA Ltd

Sales Manager - Part time

Chicago, IL · Remote

ISO Standards - which includes: * 1. ISO Implementation * 2. ISO Consultation * 3. ISO ... Document Management System (DMS), * 6. Service Desk Plus (SDP), * 7.Service Management Systems (SMS ...

Floor & Decor

Inventory Control Specialist

Chicago, IL

$16.70 - $23.90/hr

Full-Time and Part-Time Positions Available. Minimum Eligibility Requirements * One year of ... Review shipping and receiving documents for accuracy. * Bring to the attention of the department ...

Floor & Décor

Inventory Control Specialist

Chicago, IL

$16.70 - $23.90/hr

Full-Time and Part-Time Positions Available. Minimum Eligibility Requirements * One year of ... Review shipping and receiving documents for accuracy. * Bring to the attention of the department ...

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All JobsIso Document Control JobsPart Time Iso Document Control JobsPart Time Iso Document Control Jobs in Chicago, IL

Part Time Iso Document Control information

See Chicago, IL salary details

$10

$22

$31

How much do part time iso document control jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for part time iso document control in Chicago, IL is $22.39, according to ZipRecruiter salary data. Most workers in this role earn between $17.84 and $25.77 per hour, depending on experience, location, and employer.

What is a part time ISO document control?

A Part Time ISO Document Control job involves managing, organizing, and maintaining documents related to ISO standards and quality management systems for an organization. This role typically includes tasks such as updating, distributing, and archiving controlled documents, ensuring compliance with company and regulatory requirements, and supporting audits. Working part-time means the role has reduced hours compared to a full-time position, making it suitable for individuals seeking flexible work arrangements. Strong attention to detail and familiarity with document management systems are important for this job.

What are the key skills and qualifications needed to thrive as a part time ISO document control?

To thrive as a Part Time ISO Document Control, you need strong organizational skills, attention to detail, and a good understanding of ISO standards, typically supported by experience in document management or quality assurance. Familiarity with document control software, electronic document management systems (EDMS), and sometimes ISO 9001 certification is often required. Excellent communication, time management, and the ability to work independently are valuable soft skills for this role. These skills ensure accurate documentation, compliance with quality standards, and efficient workflow in regulated environments.

What are some common challenges faced by part time ISO document control professionals, and how can they be effectively managed?

Part-time ISO Document Control professionals often face the challenge of staying updated with frequent document revisions and ensuring timely communication across departments, despite limited work hours. Balancing workload and maintaining document accuracy requires strong organizational skills and efficient time management. Proactively setting clear priorities, utilizing document management systems, and maintaining open communication with team members can help manage these challenges and ensure compliance with ISO standards.

What is the difference between Part Time Iso Document Control vs Part Time Quality Assurance Coordinator?

AspectPart Time Iso Document ControlPart Time Quality Assurance Coordinator
CredentialsISO standards knowledge, basic administrative skillsQuality assurance certifications, administrative skills
Work EnvironmentOffice setting, document management systemsOffice or plant environment, quality processes
Industry UsageManufacturing, engineering, or compliance sectorsManufacturing, healthcare, or service industries
Common Search IntentManaging ISO documentation, compliance tasksMonitoring quality processes, audits

Part Time Iso Document Control focuses on managing ISO-related documents and ensuring compliance with standards, while Part Time Quality Assurance Coordinator oversees quality processes and audits. Both roles require administrative skills but differ in their specific focus areas within the industry.

What are the most commonly searched types of Iso Document Control jobs in Chicago, IL?

The most popular types of Iso Document Control jobs in Chicago, IL are:

What are popular job titles related to Part Time Iso Document Control jobs in Chicago, IL?

For Part Time Iso Document Control jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Part Time Iso Document Control jobs in Chicago, IL look for?

The top searched job categories for Part Time Iso Document Control jobs in Chicago, IL are:

Part Time Iso Document Control jobs near you
Infographic showing various Part Time Iso Document Control job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 19% Part Time, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $46,564 per year, or $22.4 per hour.

Document Specialist (Part-TIme)

Portage, IN

Ursitti Enterprises LLC
See more jobs at Ursitti Enterprises LLCexternal

$19 - $20/hr

Part-time

Re-posted 21 days ago

Job description

Leading Pharmaceutical Manufacturer Requires a Part-Time 1st Shift Document Specialist at their Portage Facility! If you meet the qualifications below, APPLY NOW!

$20.00/Hour


Job Description:

We seek a meticulous and organized Document Specialist to join our client's team in Portage. As a Document Specialist, you will be crucial in managing and maintaining various documents critical to their operations, including regulatory submissions, standard operating procedures (SOPs), clinical trial documents, and other essential records.

Responsibilities:

  • Document Management: Ensure the accurate and timely creation, revision, and maintenance of documents, adhering to established guidelines and regulatory requirements.
  • Quality Control: Perform thorough quality checks on documents to ensure accuracy, consistency, and compliance with internal standards and regulatory guidelines.
  • Document Review: Review documents for completeness, correctness, and clarity, collaborating with relevant stakeholders to address discrepancies or issues.
  • Version Control: Manage document versions effectively, maintaining a clear and organized version history to facilitate tracking and retrieval.
  • Documentation Support: Support various departments by assisting in preparing, formatting, and distributing documents as needed.
  • Training and Compliance: Assist in training employees on document management processes and procedures to ensure compliance with company policies and regulatory standards.
  • Continuous Improvement: Identify opportunities for process improvements and efficiency enhancements within the document management system.

Qualifications:

  • Bachelor's degree or equivalent experience in a relevant field of life sciences, business administration, or related discipline).
  • Previous experience in document management, preferably within the pharmaceutical or healthcare industry.
  • Strong attention to detail and excellent organizational skills, with the ability to effectively manage multiple tasks and priorities.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and document management software.
  • Familiarity with regulatory requirements (e.g., FDA, EMA) and industry standards (e.g., GCP, GMP) preferred.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams.