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Iso Document Control Jobs in Florida (NOW HIRING)

Alliance Workforce

Quality Control

Pinellas Park, FL

$16.25 - $20.75/hr

Perform quality testing and document inspection results. * Record and analyze data using quality ... Follow all safety, quality, and ISO procedures. * Assist with continuous process improvement ...

BRPH

Construction Drafter

Melbourne, FL · On-site

Maintain drawing files, revision histories, and document control procedures. Support multiple ... Knowledge of ANSI, ISO, or client-specific drafting standards. Performance Expectations Accuracy ...

WTEC

Quality Control Inspector

Milton, FL · On-site

$16 - $18/hr

We are an ISO-9001 Certified OEM manufacturer. The selected individual will be part of a growing ... documentation as it relates to daily inspection process or lab test. Assist in the processing of ...

BRPH

Construction Drafter

Melbourne, FL · On-site

... and document control to produce timely, accurate drawings that facilitate successful project ... ISO, or client-specific drafting standards. Performance Expectations • Accuracy and quality of ...

Actalent

Quality Engineer

Miami, FL

$68K - $88K/yr

Maintain and oversee document control processes to ensure accurate, current, and compliant quality ... Familiarity with ISO and Good Manufacturing Practice (GMP) requirements. * Proficiency in root ...

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Iso Document Control information

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How much do iso document control jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for iso document control in Florida is $16.24, according to ZipRecruiter salary data. Most workers in this role earn between $12.93 and $18.70 per hour, depending on experience, location, and employer.

Is iso document control a stressful job?

ISO document control is generally a detail-oriented role that involves managing and maintaining quality management system documents, which can be repetitive but typically does not involve high stress levels. The job requires accuracy, organization, and familiarity with standards like ISO 9001, and workload may vary depending on company size and project deadlines.

Is document control a stressful job?

Document control roles, such as ISO document control specialists, involve managing and maintaining accurate records, which can be detail-oriented and require strict adherence to deadlines. The job can be stressful during busy periods or when handling large volumes of documents, but effective organization and familiarity with document management systems can help reduce stress.

What qualifications do I need to be an ISO Document Control?

To be an ISO Document Control professional, candidates typically need a high school diploma or equivalent, with many roles preferring or requiring a bachelor's degree in fields like quality management, business, or engineering. Strong organizational skills, attention to detail, familiarity with document management systems, and knowledge of ISO standards such as ISO 9001 are important qualifications for this role.

What are the key skills and qualifications needed to thrive in the ISO document control position, and why are they important?

To excel as an ISO Document Control specialist, strong attention to detail, organizational skills, and a good understanding of document management systems are essential, often supported by experience or certification in ISO standards like ISO 9001. Familiarity with electronic document management software (EDMS), version control systems, and auditing tools is typically required. Excellent communication, time management, and the ability to work collaboratively with various departments are valuable soft skills in this role. These competencies are crucial for maintaining compliance, ensuring document accuracy, and supporting smooth audits and process improvements.

What does an ISO document control do?

An ISO Document Control professional's day-to-day responsibilities often include managing document updates and revisions, distributing controlled documents to relevant teams, and ensuring all documentation complies with applicable ISO standards. They may also conduct internal audits, maintain document logs, and liaise with auditors or regulatory bodies during inspections. Collaboration with quality assurance, engineering, and management is common to ensure all team members have access to the latest procedures and records. Staying organized and maintaining consistency across documentation helps support efficient operations and successful external audits.

What is an ISO document control?

An ISO Document Control job involves managing and organizing documents to comply with ISO standards. Responsibilities include creating, reviewing, updating, and distributing controlled documents while ensuring version control and compliance with quality management systems. This role is critical for maintaining consistency, accuracy, and accessibility of documents in organizations seeking ISO certification. It often involves coordinating with different departments, conducting audits, and ensuring proper documentation practices.

What are the most commonly searched types of Iso Document Control jobs in Florida? The most popular types of Iso Document Control jobs in Florida are:
What are popular job titles related to Iso Document Control jobs in Florida? For Iso Document Control jobs in Florida, the most frequently searched job titles are:
What job categories do people searching Iso Document Control jobs in Florida look for? The top searched job categories for Iso Document Control jobs in Florida are:
Iso Document Control jobs near you
Infographic showing various Iso Document Control job openings in Florida as of August 2026, with employment types broken down into 87% Full Time, 6% Contract, and 7% Nights. Highlights an 100% In-person job distribution, with an average salary of $33,779 per year, or $16.2 per hour.

QA/QC Specialist - Dietary Supplement Manufacturer (21 CFR 111 )

Sun Nutraceuticals

Fort Lauderdale, FL • On-site

$23 - $30.75/hr

Full-time

Re-posted 3 days ago

Job description

We are a fast-growing dietary supplement manufacturer operating in compliance with 21 CFR Part 111, seeking a hands-on QA/QC professional who is motivated by building, strengthening, and refining quality systems—not simply maintaining the status quo.
This role combines daily QA/QC execution (including raw materials & product receiving, in-process and final reviews for materials / documentation, material quarnatines and releases, and document control) with active Quality Management System development. Responsibilities include writing and reviewing SOPs, MMRs, and BPRs; supporting supplier qualification; strengthening CAPA effectiveness; and contributing to GMP training programs. You will partner closely with Quality leadership to enhance process consistency, reduce errors, and elevate our long-term “inspection-ready” posture.
The ideal candidate is comfortable operating in a dynamic, growing environment and is eager to help establish structure, drive continuous improvement, and ensure those improvements are sustainable.
 
What you’ll do
Quality System Continuous Improvement
Partner with Quality leadership to identify compliance gaps, prioritize improvements, and execute a practical roadmap across documentation, training, supplier qualification, and CAPA.
  • Improve how we work by standardizing templates and workflows (SOPs, forms, logs, batch packets) to reduce human error and rework.
  • Strengthen specifications, acceptance criteria, and review workflows so release decisions are consistent and fast.
  • Help establish quality metrics (doc errors, deviations, supplier performance, training completion) and drive corrective/preventive actions.
Documentation & Record Control
  • Draft, revise, and version-control SOPs, Work Instructions, forms, and logbooks; route for review/approval; train teams on changes.
  • Build and maintain Master Manufacturing Records (MMRs) (21 CFR 111.210) and ensure executed Batch Production Records (BPRs) (111.260) are complete, legible, and compliant.
  • Support document change control (redlines, impact assessments, training, effective dates).
Quality Control Operations
  • Perform/coordinate receiving inspections, in-process checks, line clearance, label reconciliation, and finished product release/quarantine per specifications.
  • Support sampling plans (ANSI/ASQ Z1.4 / ISO 2859), retain management, and reserve samples (111.83).
Supplier & Material Qualification
  • Maintain the Approved Supplier List; collect/assess questionnaires, audits, and performance data.
Deviations, Investigations & CAPA
  • Log and investigate deviations/OOS/OOT and drive CAPA through effectiveness checks.
  • Track trends and propose preventive actions to reduce repeats.
What you’ll bring
Minimum (one of the following)
  • 1+ year in a QA or QC role in dietary supplements or food/beverage.
  • Relevant education/training (degree in relevant field, GMP certifications, etc.) demonstrating readiness to perform regulated QA/QC work.
Bonus points if you have
  • Experience supporting regulatory inspections or GMP certification audits.
  • Experience with Lean Manufacturing / Six Sigma
  • Experience with cloud-based ERP/MRP platforms.
  • Experience developing/reviewing product specifications.
  • Experience developing/reviewing product packaging and labeling.
  • Solid Excel/Google Sheets skills (filters, pivot tables, lookups) and comfort learning digital tools (we use digital systems and expect you to learn quickly).
Physical & work environment
  • Stand/walk on a production floor; lift up to 50 lbs occasionally; wear PPE; work around food-grade solvents and flavors.
  • Adhere to hygiene, gowning, allergen, and sanitation rules.
  • Must have reliable transportation; role may include traveling between sites.
  • Must be willing to work early/later than business hours on occasion.