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Gmp Technical Writer Jobs (NOW HIRING)

INCOG

Engineering Technical Writer

Fishers, IN

Author, revise, and maintain engineering GMP documentation (SOPs, work instructions, prep forms, IQ ... Minimum of 3 years of technical writing experience, preferably within a regulated GMP environment ...

BioPhase Solutions

CA · On-site

$36 - $41/hr

Ensure compliance with GMP, ISO 90001, regulatory requirements, dept/bldg. Safety rules and applicable company policies and procedures * Support cross functional teams by providing technical writing ...

USWM, LLC

Technical Writer

Philadelphia, PA · On-site

$92K - $117K/yr

The Technical Writer, Facilities is responsible for creating, maintaining, and improving written ... Experience with GMP Quality Management Systems (i.e deviations, change controls, investigations ...

New

Pacer Group

Admin - Assoc Spec, Technical Writing

Irvine, CA · On-site

$24.50 - $30.75/hr

The main function of a technical writing specialist is to develop and create accurate Good Manufacturing Practices (GMP) technical documents. Key Responsibilities: • Collect data and testing ...

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How much do gmp technical writer jobs pay per hour?

As of Sep 11, 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, 85% Full Time, 10% Part Time, 2% 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

Franklin, OH

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Integrated Resources INCexternal

Contractor

Re-posted 5 days ago

Job description

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Looking for GMP experience in addition to tech writer experience. Also, this person will also be summarizing metrics for the site so some data extraction and spreadsheet experience will be required.Technical Writing role writes, or supports the development of, various technical documents such as: requirements, specifications, test plans, and user manuals.

Qualifications
  • Understands validation concepts in order to produce documentation for validated systems;
  • Provides evidence of compliance with legal, business and regulatory requirements;
  • Translates highly technical software functions/features into process driven user friendly materials to support implementation and training of applications;
  • Liaises with clients or developers to gather information; 
  • Organizes, synthesizes medical and business literature, and writes clear, accurate reviews of the literature. 
  • Creates operational and system qualification documentation in support of Messaging Services implementation.
  •  Develops Standard Operating Procedures (SOPs), training materials, and user manuals.
  • Bachelor's Degree is must.
Additional Information

Thanks!!
With Regards,
Sasha Sharma
Clinical Recruiter
Integrated Resources, Inc
IT REHAB CLINICAL NURSING
Direct: 732-662-7964 | (W) 732-549-2030 x 219

Inc. 5000 - 2007-2015 (9 Years in a row)

Integrated Resources logo

About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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