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Technical Writer Jobs in Riverside, CA (NOW HIRING)

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Technical Writer

Rancho Cucamonga, CA · On-site

$31 - $35.50/hr

ON-SITE TECHNICAL WRITER ID: 900064 Department: Marketing Starting Wage or Wage Range: $31.00 - $35.50 Why join the General Micro Systems team? Since its inception in 1979, General Micro Systems has ...

Quality Technical Writer We are seeking a skilled Quality Technical Writer to join our team. The ideal candidate will excel in technical report writing and will be working in a contained facility lab ...

ClifyX is a company that specializes in technical documentation, and they are seeking a Technical Writer to create documentation for Rivian hardware and software. The role involves collaborating with ...

Criterion Writer 2026-27

Riverside, CA · On-site

$16.90 - $17.40/hr

A writer for any Criterion section is expected to write various Criterion pieces per quarter, depending on need and after receiving explicit instruction from the editorial team. * All writers are ...

Coordinate and review consultant technical specifications for conformance with firm standards and ... Minimum of 3 years of increased responsibility in writing, editing, and developing AIA MasterFormat ...

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Technical Writer information

See Riverside, CA salary details

$14

$40

$68

How much do technical writer jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for technical writer in Riverside, CA is $40.63, according to ZipRecruiter salary data. Most workers in this role earn between $30.10 and $49.13 per hour, depending on experience, location, and employer.

What is the difference between Technical Writer vs Technical Editor?

AspectTechnical WriterTechnical Editor
Primary RoleCreates and develops technical documentation, manuals, and guides.Reviews, revises, and ensures clarity and accuracy of technical content.
Skills & CertificationsStrong writing, communication, and technical knowledge; certifications like STC are common.Editing skills, attention to detail, and technical understanding; often holds editing certifications.
Work EnvironmentCollaborates with engineers, product teams, and subject matter experts.Works closely with writers and subject matter experts to refine content.
Industry UsageUsed across tech, manufacturing, software, and engineering sectors.Commonly employed in publishing, software, and technical fields for quality control.

While both roles require technical knowledge and strong communication skills, Technical Writers focus on creating content, whereas Technical Editors concentrate on reviewing and improving existing documentation. Both roles are essential for producing clear, accurate technical materials in various industries.

How does a technical writer typically collaborate with subject matter experts (SMEs) during documentation projects?

Technical Writers frequently work closely with subject matter experts to gather accurate information and clarify complex concepts. This collaboration often involves conducting interviews, attending product demos, and reviewing drafts together to ensure technical accuracy and clarity. Building a strong rapport with SMEs is essential, as it helps streamline the review process and results in higher-quality documentation. Effective communication and a proactive approach are key to overcoming challenges such as limited SME availability or evolving product features.

What are the key skills and qualifications needed to thrive as a technical writer, and why are they important?

To thrive as a Technical Writer, you need strong writing, editing, and research skills, often supported by a degree in English, communications, or a related field. Familiarity with documentation tools such as Microsoft Word, Adobe FrameMaker, MadCap Flare, and content management systems is typically required. Attention to detail, the ability to simplify complex information, and effective collaboration are crucial soft skills for this role. These competencies ensure the creation of clear, accurate, and user-friendly documentation that supports product usability and end-user satisfaction.

Is technical writing still in demand?

Technical writing remains in demand across industries such as technology, healthcare, and engineering, as companies require clear documentation for products, processes, and compliance. Skilled technical writers with knowledge of tools like Markdown, XML, or content management systems are especially sought after, and the role often requires strong communication and technical skills. The demand is expected to grow with increasing complexity in products and regulatory requirements.

Are technical writers paid well?

Technical writers are generally paid competitive salaries that vary based on experience, industry, and location. Entry-level positions typically start lower, while experienced technical writers with specialized skills or certifications can earn higher wages, especially in technology and engineering sectors.

Can you work remotely as a technical writer?

Many technical writers have the option to work remotely, especially those with strong writing, communication, and technical skills. Remote work arrangements depend on the employer and project requirements, and tools like documentation platforms and collaboration software facilitate remote collaboration.
What are the most commonly searched types of Technical Writer jobs in Riverside, CA? The most popular types of Technical Writer jobs in Riverside, CA are:
What are popular job titles related to Technical Writer jobs in Riverside, CA? For Technical Writer jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Technical Writer jobs in Riverside, CA look for? The top searched job categories for Technical Writer jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Technical Writer jobs? Cities near Riverside, CA with the most Technical Writer job openings:
Infographic showing various Technical Writer job openings in Riverside, CA as of July 2026, with employment types broken down into 92% Full Time, 5% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $84,506 per year, or $40.6 per hour.

$68K - $96K/yr

Full-time

Re-posted 2 days ago


Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

68th of 536 rated manufacturers


Job description

Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) team, part of the AI, Product and Platforms organization, is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It is our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
At Edwards Lifesciences, the IHFM AI, Product and Platforms organization designs and builds the software and data products that clinicians and patients depend on. As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated software traceable and audit ready. You produce and maintain design control artifacts and user-facing documentation with limited guidance, partnering with engineering, quality, and product.
Based in Irvine, CA, you'll join a high-impact medtech innovation hub in the heart of Orange County, collaborating in person with cross-functional teams to shape patient-focused technology.
How You'll Make an Impact
  • Create and maintain moderately complex Good Manufacturing Practices (GMP) protocols, reports, technical summaries, and test procedures.
  • Develop well-scoped controlled documentation that supports regulated software traceability and audit readiness.
  • Maintain documentation in a standard format and follow established guidelines for content quality, organization, and consistency.
  • Partner with production employees, technicians, engineers, project teams, regulatory partners, and management to understand product, component, or device changes.
  • Review documents for style, clarity, grammar, punctuation, and overall usability.
  • Identify and resolve inconsistencies in content, structure, or document development, and work with authors to recommend appropriate updates.
  • Respond to requests for clarification or explanation of reference materials and technical documentation.
  • Support additional documentation-related needs as assigned by leadership.

What you'll need (Required):
  • Bachelor's degree in a related field and 3 years of technical writing experience, or equivalent work experience based on Edwards criteria.
  • Relocation is not provided for this role. Only candidates within a 50-mile radius of Irvine, California will be considered.

What else we look for (Preferred):
  • Biotechnology, medical device, or regulated industry experience, or equivalent work experience based on Edwards criteria.
  • Experience creating or maintaining documentation types such as procedures, routers, process sheets, technical summaries, protocols, and test reports.
  • Solid understanding of policies, procedures, and guidelines relevant to technical documentation development.
  • Strong editing, proofreading, and technical writing skills, with careful attention to style, clarity, grammar, and punctuation.
  • Proficiency with Microsoft Office Suite, including Word, Excel, PowerPoint, and Publisher; Adobe and Photoshop experience preferred.
  • Good written and verbal communication skills in English, with strong interpersonal skills.
  • Good problem-solving, critical thinking, organization, and prioritization skills in a fast-paced environment.
  • Ability to work independently on more complex projects or lines of work, with work reviewed for accuracy and soundness.
  • Ability to collaborate across interdepartmental teams, build productive internal and external working relationships, and represent the organization on specific projects.
  • Strict attention to detail and commitment to following all company rules and requirements, including Environmental Health & Safety expectations and applicable protocols.

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California (CA), the base pay range for this position is $68,000 to $96,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.
COVID Vaccination Requirement
Edwards is committed to protecting our vulnerable patients and the healthcare providers who are treating them. As such, all patient-facing and in-hospital positions require COVID-19 vaccination. If hired into a covered role, as a condition of employment, you will be required to submit proof that you have been vaccinated for COVID-19, unless you request and are granted a medical or religious accommodation for exemption from the vaccination requirement. This vaccination requirement does not apply in locations where it is prohibited by law to impose vaccination.

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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958