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Quality Systems / Technical Documentation Specialist

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Onsite

Quality Systems / Technical Documentation Specialist

TAMPA BRASS & ALUMINUM

Quality Systems / Technical Documentation Specialist

Skills

ComplianceRegulatory Compliance

2 months ago

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Important information


Contract type:

Permanent

Salary:

$75,000 – $88,000 / year

Location:

Tampa, FL, USA

Work mode:

Onsite

Published on:

9 September 2026

What they need


Position Summary

The Quality Systems / Technical Documentation Specialist is responsible for maintaining and improving the organization's Quality Management System (QMS) while ensuring technical documentation is accurate, controlled, and compliant with industry and customer requirements. This position supports manufacturing, engineering, and quality teams by administering document control processes, managing quality records, coordinating audits, and maintaining procedures, work instructions, specifications, and technical documentation.

The ideal candidate has experience in manufacturing, aerospace, defense, foundry, or metal casting environments and possesses a strong understanding of quality systems, document control, and regulatory compliance.

Essential Duties & Responsibilities

  • Administer and maintain the Quality Management System (QMS) in accordance with company standards and applicable industry requirements.
  • Create, revise, format, distribute, and control technical documents, including:
  • Standard Operating Procedures (SOPs)
  • Work Instructions
  • Quality Procedures
  • Engineering Specifications
  • Inspection Plans
  • Forms and Templates
  • Process Flow Documents
  • Ensure document revisions are properly reviewed, approved, released, and archived.
  • Maintain document revision history and document retention requirements.
  • Coordinate document change requests (DCRs/ECRs/ECOs) with Engineering, Manufacturing, and Quality.
  • Support internal, customer, and third-party audits by organizing documentation and quality records.
  • Maintain quality records in compliance with retention requirements.
  • Assist with CAPA (Corrective and Preventive Actions) documentation and follow-up activities.
  • Track nonconformances and assist with documentation associated with NCRs.
  • Monitor QMS metrics and prepare quality reports as requested.
  • Support ISO 9001, AS9100, or other quality management system compliance initiatives.
  • Maintain training records associated with controlled procedures and work instructions.
  • Ensure obsolete documents are removed from points of use.
  • Coordinate periodic document reviews with department owners.
  • Assist Engineering with Bill of Materials (BOMs), specifications, and technical drawing documentation control.
  • Maintain confidentiality of proprietary technical documentation.

Required Qualifications

  • Associate's or Bachelor's degree in Quality, Engineering Technology, Business, Technical Writing, Manufacturing, or related field preferred.
  • Minimum 3 years of experience in Quality Systems, Document Control, or Technical Documentation in a manufacturing environment.
  • Experience maintaining Quality Management Systems (QMS).
  • Strong understanding of document control processes.
  • Experience supporting audits.
  • Excellent organizational and record management skills.
  • Strong written and verbal communication skills.
  • High attention to detail and accuracy.
  • Ability to manage multiple projects and priorities simultaneously.

Preferred Qualifications

Experience with one or more of the following:

  • ISO 9001
  • AS9100
  • NADCAP documentation
  • Aerospace or Defense manufacturing
  • Metal Casting or Foundry operations
  • ERP/MRP systems
  • Electronic Document Management Systems (EDMS)
  • Microsoft SharePoint
  • PLM systems
  • Engineering Change Orders (ECO)
  • Corrective Action systems (CAPA)

Technical Skills

  • Microsoft Office Suite (Word, Excel, Outlook, PowerPoint)
  • Adobe Acrobat
  • SharePoint
  • ERP/MRP software
  • Document Management Systems
  • Quality Management Software
  • Ability to read engineering drawings and specifications
  • Basic understanding of GD&T is preferred

Key Competencies

  • Attention to Detail
  • Technical Writing
  • Document Control
  • Quality Systems Administration
  • Regulatory Compliance
  • Organization and Time Management
  • Continuous Improvement
  • Root Cause Documentation
  • Communication Skills
  • Collaboration across Engineering, Manufacturing, and Quality teams

Physical Requirements

  • Ability to work in both office and manufacturing environments.
  • Ability to sit, stand, and walk for extended periods.
  • Ability to lift up to 25 pounds occasionally.
  • Must be able to access manufacturing and production areas while wearing required PPE.

Preferred Industry Experience

Candidates with experience in one or more of the following industries are strongly preferred:

  • Aerospace Manufacturing
  • Defense Manufacturing
  • Metal Casting / Foundry
  • Precision Machining
  • Heavy Manufacturing
  • Industrial Manufacturing

Preferred Certifications (Desired but Not Required)

  • Certified Quality Improvement Associate (CQIA)
  • Certified Quality Technician (CQT)
  • Certified Quality Auditor (CQA)
  • ASQ Certified Quality Engineer (CQE)
  • ISO 9001 or AS9100 Internal Auditor Training
  • Lean Six Sigma Green Belt (preferred)

This position is ideal for a detail-oriented quality professional who enjoys maintaining robust quality systems, ensuring documentation accuracy, and supporting regulatory compliance while collaborating across engineering and manufacturing teams.

Pay: $75,000.00 - $88,000.00 per year

Benefits:

  • 401(k)
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Vision insurance

Work Location: In person

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