Associate Document Control Specialist (Hybrid) Duration: 12 Months Location: Chicago, IL Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered. The ...
Associate Document Control Specialist (Hybrid) Duration: 12 Months Location: Chicago, IL Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered. The ...
Quality Assurance Document Control Specialist Lead Department: Quality Assurance Employment Type ... Associate's or Bachelor's degree in Quality, Life Sciences, Manufacturing, Business, or a related ...
Quality Assurance Document Control Specialist Lead Department: Quality Assurance Employment Type ... Associate's or Bachelor's degree in Quality, Life Sciences, Manufacturing, Business, or a related ...
Specialist, Document Control
Newton, IA ยท On-site
The Specialist, Document Control & Calibration Support is responsible for maintaining and controlling quality management system documentation while supporting laboratory calibration activities to ...
Specialist, Document Control
Newton, IA ยท On-site
The Specialist, Document Control & Calibration Support is responsible for maintaining and controlling quality management system documentation while supporting laboratory calibration activities to ...
The Quality Assurance Document Control Specialist Lead is responsible for leading and maintaining ... Associate's or Bachelor's degree in Quality, Life Sciences, Manufacturing, Business, or a related ...
The Quality Assurance Document Control Specialist Lead is responsible for leading and maintaining ... Associate's or Bachelor's degree in Quality, Life Sciences, Manufacturing, Business, or a related ...
Associate Document Control Specialist (Hybrid)
Chicago, IL ยท On-site
$40/hr
Associate Document Control Specialist (Hybrid) Duration: 12 Months Location: Chicago, IL Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered. The ...
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Associate Document Control Specialist (Hybrid)
Chicago, IL ยท On-site
$40/hr
Associate Document Control Specialist (Hybrid) Duration: 12 Months Location: Chicago, IL Only W2 candidates are eligible for this position. Third-party or C2C candidates will not be considered. The ...
QA Document Control
Mckinney, TX ยท On-site
QA Document Control Duties: Control and reconcile labels. Review completed batch production records. Provide customer service. Regulatory compliance in accordance with FDA 21 CFR 111 guidance.
New
QA Document Control
Mckinney, TX ยท On-site
QA Document Control Duties: Control and reconcile labels. Review completed batch production records. Provide customer service. Regulatory compliance in accordance with FDA 21 CFR 111 guidance.
New
RA/QA Associate
Pearl, MS ยท On-site
This role plays a key part in complaint handling, regulatory reporting, document control ... in RA, QA, or manufacturing within a regulated industry (medical device preferred). Associate ...
RA/QA Associate
Pearl, MS ยท On-site
This role plays a key part in complaint handling, regulatory reporting, document control ... in RA, QA, or manufacturing within a regulated industry (medical device preferred). Associate ...
QA Associate Onsite in Flanders, NJ and Fairfield, NJ Garonit Pharma is seeking a detail-oriented ... Experience supporting QC systems and auditing laboratory documentation/data is strongly preferred
QA Associate Onsite in Flanders, NJ and Fairfield, NJ Garonit Pharma is seeking a detail-oriented ... Experience supporting QC systems and auditing laboratory documentation/data is strongly preferred
You will perform review of Production batch records and control records for OTC products and ... You have two years' knowledge of pharmaceutical GMP documentation requirements and quality ...
You will perform review of Production batch records and control records for OTC products and ... You have two years' knowledge of pharmaceutical GMP documentation requirements and quality ...
You will perform review of Production batch records and control records for OTC products and ... You have two years' knowledge of pharmaceutical GMP documentation requirements and quality ...
You will perform review of Production batch records and control records for OTC products and ... You have two years' knowledge of pharmaceutical GMP documentation requirements and quality ...
Document Control Specialist
Chicago, IL ยท Hybrid
$46.49/hr
The Document Control Specialist position is part of the (Associate Document Control Specialist and ... This role serves as a final point of quality control by verifying that all required approvals have ...
Document Control Specialist
Chicago, IL ยท Hybrid
$46.49/hr
The Document Control Specialist position is part of the (Associate Document Control Specialist and ... This role serves as a final point of quality control by verifying that all required approvals have ...
GMP Document Management
Lebanon, NJ ยท On-site
$22/hr
As a Senior QA Associate, you will work closely with the QA team to maintain document control systems, manage archival processes, and ensure the accuracy and accessibility of quality records across ...
GMP Document Management
Lebanon, NJ ยท On-site
$22/hr
As a Senior QA Associate, you will work closely with the QA team to maintain document control systems, manage archival processes, and ensure the accuracy and accessibility of quality records across ...
Document Control Specialist
Chicago, IL ยท Hybrid
$46.49/hr
The Document Control Specialist position is part of the (Associate Document Control Specialist and ... This role serves as a final point of quality control by verifying that all required approvals have ...
Document Control Specialist
Chicago, IL ยท Hybrid
$46.49/hr
The Document Control Specialist position is part of the (Associate Document Control Specialist and ... This role serves as a final point of quality control by verifying that all required approvals have ...
In this role, you are responsible for supporting Quality Assurance Operations activities at Artiva ... Solid background in document control, prior experience working with electronic quality management ...
Quick apply
In this role, you are responsible for supporting Quality Assurance Operations activities at Artiva ... Solid background in document control, prior experience working with electronic quality management ...
In this role, you are responsible for supporting Quality Assurance Operations activities at Artiva ... Solid background in document control, prior experience working with electronic quality management ...
In this role, you are responsible for supporting Quality Assurance Operations activities at Artiva ... Solid background in document control, prior experience working with electronic quality management ...
Quality Assurance Associate
New Lisbon, WI ยท On-site
We are looking for a Quality Assurance Associate in New Lisbon, WI. Schedule: Monday - Friday, 8:00 ... Quality Assurance Plant Document Control. This list of duties and responsibilities is not all ...
Quality Assurance Associate
New Lisbon, WI ยท On-site
We are looking for a Quality Assurance Associate in New Lisbon, WI. Schedule: Monday - Friday, 8:00 ... Quality Assurance Plant Document Control. This list of duties and responsibilities is not all ...
Quality Assurance Associate
Lisbon, WI ยท On-site
We are looking for a Quality Assurance Associate in New Lisbon, WI. Schedule: Monday - Friday, 8:00 ... Quality Assurance Plant Document Control. This list of duties and responsibilities is not all ...
Quality Assurance Associate
Lisbon, WI ยท On-site
We are looking for a Quality Assurance Associate in New Lisbon, WI. Schedule: Monday - Friday, 8:00 ... Quality Assurance Plant Document Control. This list of duties and responsibilities is not all ...
The QA Associate will need to provide support with identifying operational and quality gaps. The ... Review and approve documentation for Quality approval, including but not limited to on-floor batch ...
The QA Associate will need to provide support with identifying operational and quality gaps. The ... Review and approve documentation for Quality approval, including but not limited to on-floor batch ...
Quality Document Control Specialist
Fuquay Varina, NC ยท On-site
$30 - $35/hr
Support QA/QC teams in training employees on GDP and cGMP requirements. Communicate process updates ... Some advanced education is preferred (Associate's or Bachelor's degree a plus). * 3 years' minimum ...
Quality Document Control Specialist
Fuquay Varina, NC ยท On-site
$30 - $35/hr
Support QA/QC teams in training employees on GDP and cGMP requirements. Communicate process updates ... Some advanced education is preferred (Associate's or Bachelor's degree a plus). * 3 years' minimum ...
Quality Assurance Document Control Associate II
Clifton, NY ยท On-site
$22.53 - $29/hr
The Quality Assurance Document Control Associate is responsible for the administration, maintenance, and control of Quality Management System (QMS) documentation in accordance with the requirements ...
Quality Assurance Document Control Associate II
Clifton, NY ยท On-site
$22.53 - $29/hr
The Quality Assurance Document Control Associate is responsible for the administration, maintenance, and control of Quality Management System (QMS) documentation in accordance with the requirements ...
Qa Associate Specialist Document Control information
See salary details
$11.30 - $14.47
13% of jobs
$14.47 - $17.64
6% of jobs
$18.36 is the 25th percentile. Wages below this are outliers.
$17.64 - $20.80
25% of jobs
The median wage is $22.14 / hr.
$20.80 - $23.97
14% of jobs
$23.97 - $27.14
8% of jobs
$27.14 - $30.31
5% of jobs
$32.01 is the 75th percentile. Wages above this are outliers.
$30.31 - $33.48
8% of jobs
$33.48 - $36.65
11% of jobs
$36.65 - $39.82
2% of jobs
$39.82 - $42.99
3% of jobs
$42.99 - $46.15
5% of jobs
$11
$26
$46
How much do qa associate specialist document control jobs pay per hour?
What are the key skills and qualifications needed to thrive as a QA Associate Specialist Document Control, and why are they important?
What does a QA Associate Specialist in Document Control do?
What are some common challenges faced by a QA Associate Specialist in Document Control, and how can they be managed effectively?
What is the difference between Qa Associate Specialist Document Control vs Qa Associate Specialist Quality Assurance?
| Aspect | Qa Associate Specialist Document Control | Qa Associate Specialist Quality Assurance |
|---|---|---|
| Primary Focus | Managing and controlling documentation, ensuring document accuracy and compliance | Ensuring product quality through testing, inspections, and process audits |
| Key Responsibilities | Document review, version control, record keeping | Product testing, process validation, quality audits |
| Required Credentials | Typically a degree in life sciences or related field, familiarity with document management systems | Similar educational background, knowledge of quality standards and testing procedures |
| Work Environment | Office-based, document management systems, regulated industries | Laboratory or manufacturing settings, quality labs |
While both roles support quality processes, the Qa Associate Specialist Document Control primarily manages documentation and records, whereas the Qa Associate Specialist Quality Assurance focuses on product testing and process validation. Both positions require similar credentials and are essential in regulated industries like pharmaceuticals and biotech.

Contractor
Posted 24 days ago
Job description
Title: Associate Document Control Specialist (Hybrid)
Duration: 12 Months
Location: Chicago, IL
Only W2 candidatesare eligible for this position. Third-party or C2C candidates will not be considered.
Job Description:
The associate document control specialist is responsible for data entry tasks associated with the project document life cycle. The Associate Specialist position collects, maintains, and distributes various electronic documents necessary to support throughout the project life cycle; maintains a comprehensive filing system and database for all documents to be retained in the document control system; manages the latest revision of all documentation in a timely manner. Associate Specialist performs mostly data entry functions into the electronic database and tracking log, including reviewing documents for minor imperfections, and making minor corrections. Associate specialist is required to review and follow all document control checklists, guidelines, and processes prior to performing their job function.
Job Duties:
- Data entry, control, metadata, release, versioning, and archiving of electronic documentation.
- Communicate and coordinate with other departments for collecting, data entry and filing all documentation relating to document life cycle. Maintain document files to be orderly, up-to-date, and ready for audit at all times.
- Respond and fulfill internal documentation requests. Printing and compiling documentation as requested.
- Light analysis and review of documents received compared to the document requirements.
- Provide feedback to the supplier of the documents as needed and make minor corrections.
Minimum Qualifications:
- High School Diploma, HSED, or GED
- 1+ years providing support on major construction programs, preferably within a utility. 1+ years of administrative and data entry experience in any setting.
- 3+ years' experience in Microsoft Office products Adobe Professional Scanning and Printing with OCE plotters and experience should include working in an electronic Document Management System