This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
New
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
New
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
New
This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and ...
New
Excellent clinical summarization and documentation review skills. * Strong communication with clinical teams and insurance reviewers. * Ability to problem-solve, escalate appropriately, and manage ...
Quick apply
Excellent clinical summarization and documentation review skills. * Strong communication with clinical teams and insurance reviewers. * Ability to problem-solve, escalate appropriately, and manage ...
Clinical Document Specialist-PBO-BHC
Fort Lauderdale, FL · On-site
$33.25 - $44.75/hr
Provides a clinically based concurrent and retrospective review of inpatient medical records to evaluate the documentation of acute care services. Generates and issues compliant queries to providers ...
Clinical Document Specialist-PBO-BHC
Fort Lauderdale, FL · On-site
$33.25 - $44.75/hr
Provides a clinically based concurrent and retrospective review of inpatient medical records to evaluate the documentation of acute care services. Generates and issues compliant queries to providers ...
Utilization Review Specialist (Per Diem)
Deerfield Beach, FL · On-site
$65 - $111/hr
Excellent clinical summarization and documentation review skills. * Strong communication with clinical teams and insurance reviewers. * Ability to problem-solve, upscale appropriately, and manage ...
Utilization Review Specialist (Per Diem)
Deerfield Beach, FL · On-site
$65 - $111/hr
Excellent clinical summarization and documentation review skills. * Strong communication with clinical teams and insurance reviewers. * Ability to problem-solve, upscale appropriately, and manage ...
Post-Closing Document Specialist
Fort Lauderdale, FL · On-site
$20 - $25/hr
You'll review every page of every package, day in and day out. That precision is the whole point. These are the most critical documents in our business, including original notes and recorded ...
Post-Closing Document Specialist
Fort Lauderdale, FL · On-site
$20 - $25/hr
You'll review every page of every package, day in and day out. That precision is the whole point. These are the most critical documents in our business, including original notes and recorded ...
General Characteristics The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service ...
General Characteristics The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service ...
... documentation in Student Information System Note and request any changes/corrections that need to be made at the campus level The Financial Aid Reviewer role is primarily focused on assisting ...
... documentation in Student Information System Note and request any changes/corrections that need to be made at the campus level The Financial Aid Reviewer role is primarily focused on assisting ...
... documentation in Student Information System • Note and request any changes/corrections that need to be made at the campus level The Financial Aid Reviewer role is primarily focused on assisting ...
... documentation in Student Information System • Note and request any changes/corrections that need to be made at the campus level The Financial Aid Reviewer role is primarily focused on assisting ...
Validate documentation in Student Information System* Note and request any changes/corrections that need to be made at the campus levelThe Financial Aid Reviewer role is primarily focused on ...
Quick apply
Validate documentation in Student Information System* Note and request any changes/corrections that need to be made at the campus levelThe Financial Aid Reviewer role is primarily focused on ...
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist
Plantation, FL · On-site
$19 - $20/hr
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quick apply
Quality Control Document Specialist
Plantation, FL · On-site
$19 - $20/hr
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Director of Preconstruction
Hollywood, FL · On-site
Acts as a document reviewer and adviser for constructability and value analysis.* * Provides monthly cost analysis for all active preconstruction assignments and manages the preconstruction ...
Director of Preconstruction
Hollywood, FL · On-site
Acts as a document reviewer and adviser for constructability and value analysis.* * Provides monthly cost analysis for all active preconstruction assignments and manages the preconstruction ...
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
Quality Control Document Specialist Location: Miramar, FL Department: Quality Assurance ... Review analytical assay data for accuracy and compliance; determine acceptability of results
General Characteristics The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service ...
General Characteristics The contract writer will be responsible for drafting and reviewing documentation related to but not limited to, procurement activities, such as purchase orders, service ...
Clinical Document Specialist - BHC - FT - Days
Fort Lauderdale, FL · On-site
$33.25 - $44.75/hr
Provides a clinically based concurrent and retrospective review of inpatient medical records to evaluate the documentation of acute care services. Generates and issues compliant queries to providers ...
Clinical Document Specialist - BHC - FT - Days
Fort Lauderdale, FL · On-site
$33.25 - $44.75/hr
Provides a clinically based concurrent and retrospective review of inpatient medical records to evaluate the documentation of acute care services. Generates and issues compliant queries to providers ...
Document Reviewer information
See Boca Raton, FL salary details
$13.23 - $15.70
6% of jobs
$17.89 is the 25th percentile. Wages below this are outliers.
$15.70 - $18.17
21% of jobs
$18.17 - $20.63
18% of jobs
The median wage is $21.49 / hr.
$20.63 - $23.10
14% of jobs
$23.10 - $25.57
11% of jobs
$27.73 is the 75th percentile. Wages above this are outliers.
$25.57 - $28.04
6% of jobs
$28.04 - $30.51
7% of jobs
$30.51 - $32.97
7% of jobs
$32.97 - $35.44
3% of jobs
$35.44 - $37.91
3% of jobs
$37.91 - $40.38
3% of jobs
$13
$24
$40
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$19/hr
Full-time
Re-posted 23 days ago
Job description
A well-established pharmaceutical company in Miramar, FL is seeking an experienced and detail-oriented Quality Assurance (QA) Document Control Specialist to support its evening shift operations. This role is responsible for maintaining, reviewing, and managing GMP documentation to ensure compliance with regulatory standards. The ideal candidate is bilingual (English/Spanish), organized, and has prior experience in pharmaceutical or FDA-regulated environments.
Location: Miramar, FL
Industry: Pharmaceutical Manufacturing
Job Type: Full-Time
Schedule: Monday to Friday, 2:30 PM - 11:00 PM
Pay: $19.00 per hour
Key Responsibilities
- Maintain and control quality documentation in accordance with GMP and FDA guidelines
- Review and archive manufacturing, packaging, and testing records for accuracy and completeness
- Ensure proper version control and distribution of controlled documents (SOPs, batch records, etc.)
- Assist in audits, inspections, and internal reviews by preparing and providing requested documentation
- Support QA team in implementing document changes, updates, and approvals
- Ensure timely and accurate entry of documentation into digital or physical filing systems
- Collaborate with production, quality, and regulatory departments to ensure documentation compliance
- Report any deviations or non-conformances found in records
Qualifications
- Minimum 1-2 years of experience in document control or QA in a pharmaceutical or FDA-regulated environment
- High school diploma or equivalent required; associate or bachelor's degree preferred
- Strong knowledge of GMP, SOPs, and document control best practices
- Excellent attention to detail and organizational skills
- Bilingual (English/Spanish) - required
- Proficient in Microsoft Office (Excel, Word, Outlook)
- Ability to work independently with minimal supervision during evening shift hours
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