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Technical Write Jobs in Florida (NOW HIRING)

ASI Systems Engineering

GMP Technical Writer

Tampa, FL · On-site

$60 - $70/hr

GMP Technical Writer Contract: 5 months duration with potential for extension Location: Tampa, FL - onsite Role Summary ASI is seeking a GMP Technical Writer / SQA Specialist to support our client ...

SAIC

Technical Writer Associate

Pensacola, FL · On-site

Technical Writer/Ed Schedule: Full-Time Shift: Day Job Travel: No Minimum Clearance Required: Interim_Secret Clearance Level Must Be Able to Obtain: Secret Potential for Remote Work: ORA_HYBRID ...

Olgoonik Corporation

Sr. Technical Writer

Tampa, FL · On-site

The Technical Writer Sr. will coordinate, execute, and lead advanced writing and editing projects to communicate complex technical and procedural requirements across the SOCOM Information Environment ...

BCforward

Technical Writer

Clearwater, FL

$25/hr

Technical Writer Clearwater, FL, USA, 33764 02/06/2017 to 10/14/2017 $25/HR ON W2 ALL SHIFTS ARE AVAILABLE Must be a US Citizen Duration can go up to 2 year max 1st shift- 7:00 am - 3:00 pm (Both 1st ...

TekWissen LLC

Technical Writer - Software

Lutz, FL · On-site

$27/hr

Position: Technical Writer - Software Location: Lutz,Florida,33558 Duration: 6 Months Job Type ... Write user-friendly content that meets the needs of target audience, turning insights into language ...

SAIC

Technical Writer Associate

Pensacola, FL · On-site

Description SAIC is hiring a Technical Writer located in Pensacola, FL . This position will be supporting Training & Education Management Systems for Naval Education and Training Command (NETC). The ...

SAIC

Technical Writer Associate

Pensacola, FL · On-site

Description SAIC is hiring a Technical Writer located in Pensacola, FL . This position will be supporting Training & Education Management Systems for Naval Education and Training Command (NETC). The ...

Collabera

Technical Writer

Fort Lauderdale, FL · On-site

The Technical Writer is responsible for driving a seamless Customer Experience through writing ... This position will write and review procedural content to ensure that all business units and ...

Collabera

Technical Writer

Saint Petersburg, FL

Writes a variety of technical articles, reports, brochures, and/or manuals for documentation for a wide range of uses. May be responsible for coordinating the display of graphics and the production ...

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Technical Write information

What jobs can technical writers do?

Technical writers can work in industries such as technology, healthcare, engineering, and manufacturing, creating user manuals, technical documentation, training materials, and online help systems. They often collaborate with subject matter experts and use tools like Adobe FrameMaker, MadCap Flare, or Microsoft Word, and may require certifications in technical communication or related fields.

What is the work of a technical writer?

A technical writer creates clear and concise documentation such as user manuals, guides, and technical reports to help users understand complex information. They often collaborate with engineers and subject matter experts and use tools like Markdown or Adobe FrameMaker to produce accurate materials. Strong writing skills and knowledge of technical concepts are essential for this role.

Are technical writers still in demand?

Technical writers are still in demand across various industries, especially in technology, healthcare, and engineering, as companies need clear documentation for products and services. The role often requires proficiency with tools like Markdown, XML, or content management systems, and demand is expected to grow with increasing technological complexity.
What cities in Florida are hiring for Technical Write jobs? Cities in Florida with the most Technical Write job openings:
Technical Write jobs near you
Infographic showing various Technical Write job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 8% Part Time, 4% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

GMP Technical Writer

ASI Systems Engineering

Tampa, FL • On-site

$60 - $70/hr

Contractor

Posted 21 days ago

Job description


GMP Technical Writer
Contract: 5 months duration with potential for extension
Location: Tampa, FL - onsite
Role Summary
ASI is seeking a GMP Technical Writer / SQA Specialist to support our client's oral solid dose manufacturing operations in Tampa. The role will provide documentation and quality-system support for equipment, utilities, and facilities used in the manufacture of tablets, capsules, and powder-based products, with particular emphasis on calibration and maintenance remediation. This role will also support deviations, investigations, CAPAs, and computerized-system access controls.
Key Responsibilities
  • Author and revise GMP documents, including SOPs, WorkInstructions, deviations, investigations, CAPAs, and maintenance andcalibration procedures
  • Work with Maintenance, Calibration, Engineering,Operations, and Quality personnel to gather technical content and convertit into clear, GMP-compliant documentation
  • Support investigation writing, root-causedocumentation, corrective actions, and closure of quality-system records
  • Review and update preventive maintenance andcalibration documentation for accuracy, completeness, and alignment withcurrent practices
  • Maintain trackers for open documents, investigations,CAPAs, calibration items, maintenance actions, and approval status
  • Catalog computerized systems and online softwareplatforms used across the site
  • Review, document, and update user access, securityroles, permissions, and system ownership
  • Support periodic access reviews and removal ofinactive, duplicate, or inappropriate access
  • Coordinate document routing, review, approval, andeffective-date activities within applicable electronic quality systems
  • Support inspection-readiness anddocumentation-remediation initiatives

Requirements
Requirements
Required Qualifications
  • 3-6+ years of GMP technical writing experience inpharmaceutical, biotech, or medical-device manufacturing
  • Demonstrated experience authoring SOPs, WorkInstructions, deviations, investigations, and CAPAs
  • Experience supporting calibration, maintenance,engineering, or equipment-related documentation
  • Familiarity with electronic quality-management anddocument-control systems
  • Strong understanding of GMP documentation, dataintegrity, version control, and approval workflows
  • Ability to translate complex technical informationinto clear, compliant, and auditable documents
  • Strong organizational skills and attention to detail

Apply