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Gmp Technical Writer Jobs (NOW HIRING)

Kellton Tech

Technical Writer I

Houston, TX · On-site

$23 - $28/hr

Technical Writer I Location: Houston, TX (Onsite - 5x/week) Schedule: Monday - Friday | 1st Shift ... Review and interpret GMP documents (SOPs, logs, Batch Records) * Participate in deviation review ...

INTERACTION 24 LLC

Maintenance Technical Writer Employment Type: Contract-to-Hire | Location: Seabrook, NJ (on-site ... Familiarity with food & beverage or food-grade manufacturing environments and GMP documentation ...

Astrix Inc

Technical Writer I/II

Houston, TX · On-site

$32 - $38/hr

Qualifications * 5+ years of technical writing experience, preferably with electronic or medical ... Experience in a regulated environment (GMP/FDA) preferred. This is a complete list of all desired ...

Thermo Fisher Scientific

Technical Writer

Allentown, PA · On-site

Working Conditions and Environment: • Work is performed in an office, laboratory and/or GMP Depot environment. • For laboratory positions, potential exposure to biological fluids with potential ...

Thermo Fisher Scientific

Technical Writer

Allentown, PA · On-site

Working Conditions and Environment: • Work is performed in an office, laboratory and/or GMP Depot environment. • For laboratory positions, potential exposure to biological fluids with potential ...

Orion Group

$33 - $38/hr

Senior Technical Writer - Quality Documentation & Change Control Location: 100% Onsite- Branchburg ... Forms and other GMP-controlled documentation * Serve as an Initiator for Change Controls and manage ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Review GMP documents such as SOPs, Batch records, Logbooks to identify the root cause for the ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Review GMP documents such as SOPs, Batch records, Logbooks to identify the root cause for the ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Review GMP documents such as SOPs, Batch records, Logbooks to identify the root cause for the ...

System One

Technical Investigation Writer

Lincolnton, NC · On-site

$40/hr

Technical Investigation Writer Location: Lincolnton, NC Type: Contract Compensation: up to $40.00 ... Review GMP documents such as SOPs, Batch records, Logbooks to identify the root cause for the ...

INTERACTION 24 LLC

Maintenance Technical Writer | Employment Type | Contract-to-Hire | Location | Seabrook, NJ (on ... environments and GMP documentation requirements • Experience working alongside a CMMS ...

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Gmp Technical Writer information

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How much do gmp technical writer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for gmp technical writer in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is a GMP technical writer?

A GMP Technical Writer is a professional responsible for creating, reviewing, and maintaining documentation required for compliance with Good Manufacturing Practices (GMP) in regulated industries like pharmaceuticals, biotechnology, and medical devices. They ensure that documents such as standard operating procedures (SOPs), batch records, validation protocols, and reports meet both regulatory and company standards. Their work is crucial for meeting quality and safety requirements, supporting audits, and ensuring products are consistently produced and controlled according to quality standards.

What are the key skills and qualifications needed to thrive as a GMP technical writer?

To thrive as a GMP Technical Writer, you need a solid understanding of Good Manufacturing Practices (GMP), technical writing expertise, and often a background in life sciences or pharmaceuticals. Familiarity with document management systems, regulatory submission platforms, and quality management software is typically required. Attention to detail, excellent organizational skills, and clear communication help distinguish top performers in this role. These skills ensure accurate, compliant, and clear documentation, which is critical for regulatory approval and maintaining product quality standards.

What are some common challenges faced by GMP technical writers during the documentation process?

GMP Technical Writers often encounter challenges such as ensuring strict compliance with regulatory standards while translating complex scientific processes into clear, concise documentation. They must frequently coordinate with subject matter experts, quality assurance teams, and manufacturing staff to verify accuracy and completeness of information. Managing multiple document versions and keeping up with evolving regulations can also be demanding, requiring strong organizational skills and attention to detail. Effective communication and collaboration are key to overcoming these challenges and producing high-quality, audit-ready documents.

What is the difference between Gmp Technical Writer vs Gmp Documentation Specialist?

AspectGmp Technical WriterGmp Documentation Specialist
CredentialsTypically requires a degree in life sciences or related field; certifications like RAC or RQAP are commonSimilar credentials; often holds certifications in regulatory affairs or document management
Work EnvironmentWorks in pharmaceutical or biotech companies, focusing on creating and editing GMP documentationWorks in regulated industries, managing and maintaining GMP documents and records
Employer & Industry UsageUsed by pharmaceutical, biotech, and medical device companies for compliance documentationCommon in similar industries, focusing on document control and compliance

Both roles require knowledge of GMP regulations and strong writing skills. Gmp Technical Writers focus on creating and editing technical documents, while Gmp Documentation Specialists manage and maintain GMP records. The roles often overlap but differ mainly in scope and focus within the documentation process.

What cities are hiring for Gmp Technical Writer jobs?

Cities with the most Gmp Technical Writer job openings:

What states have the most Gmp Technical Writer jobs?

States with the most job openings for Gmp Technical Writer jobs include:

What are popular job titles related to Gmp Technical Writer jobs?

For Gmp Technical Writer jobs, the most frequently searched job titles are:

Infographic showing various Gmp Technical Writer job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 88% Full Time, 6% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

Technical Writer I

Houston, TX • On-site

Kellton Tech
See more jobs at Kellton Techexternal

$23 - $28/hr

Contractor

Re-posted 2 days ago

Job description

Job Title: Technical Writer I
Location: Houston, TX (Onsite – 5x/week)
Schedule: Monday – Friday | 1st Shift
Pay Rate: $23.00 – $28.00/hour (W2)

Position Overview:

The Technical Writer I is responsible for the tracking, management, and completion of Supply Chain Quality Records (including deviations, material recalls, and CAPAs), working closely with subject matter experts (SMEs). This role supports continuous improvement and error prevention initiatives by identifying and addressing recurring root causes. The individual will serve as a Quality Record (PR) Subject Matter Expert (SME) – Level I for the Warehouse/Supply Chain team.

Key Responsibilities:

  • Initiate, investigate, and complete Minor and Track-and-Trend process deviations
  • Write clear, cohesive, and technically sound reports for an educated but uninformed reader
  • Capture immediate actions and containment steps for events
  • Gather and analyze data across site operations
  • Perform Root Cause Analysis (RCA) and document findings
  • Review and interpret GMP documents (SOPs, logs, Batch Records)
  • Participate in deviation review board meetings and cross-functional problem solving
  • Communicate investigative status updates to stakeholders and management
  • Collaborate with QA (Raw Materials) and other departments for CAPA discussions and comments resolution
  • Observe and collect data from warehouse/lab floor processes to support investigations
  • Adhere to standard timelines and escalate issues when needed
  • Share knowledge and updates openly with team members
  • Demonstrate professionalism and respect in all interactions
  • Perform other duties as assigned

Required Knowledge & Skills:

 

Technical Expertise:

  • Experience performing RCA and leading investigations
  • Background in laboratory environments required
  • Understanding of cGMP systems and documentation standards

 

Computer Proficiency:

  • Proficient in Microsoft Excel, Word, and databases
  • Experience with TrackWise highly preferred

 

Communication & Writing:

  • Excellent technical writing skills; clear, concise, and grammatically accurate
  • Effective communicator with internal and external stakeholders

Decision Making & Problem Solving:

  • Able to manage multiple investigations and meet deadlines
  • Strong judgment in escalating issues and driving timely resolutions

Teamwork & Initiative:

  • Collaborative, dependable, and respectful
  • Open to feedback and focused on continuous self-improvement
  • Champions change and demonstrates resilience during challenges