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Medical Device Technical Writer Jobs (NOW HIRING)

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

Technical Writer

Northridge, CA · On-site +1

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

Technical Writer

Atlanta, GA · On-site

$64K - $110K/yr

About the Role The Technical Writer scopes, revises and drafts a variety of patient-facing ... Develop of a working understanding of medical device products * Work with required subject matter ...

Company Description Medical Device/ Pharmaceutical Company. The applicant will write Product Risk ... The incumbent will work with medical, technical, manufacturing, and quality groups to develop ...

Technical Writer (FDA/GMP Documentation) Location: Petaluma, CA (100% Onsite) Pay: $60 - $70/hour ... Experience supporting pharmaceutical, biotechnology, medical device, food manufacturing, or similar ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

As a Technical Reviewer, you will work with medical device manufacturers throughout their ... writing skills, client and project management. You will assess cutting edge technology that will ...

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Medical Device Technical Writer information

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$57

How much do medical device technical writer jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for medical device technical writer in the United States is $38.64, according to ZipRecruiter salary data. Most workers in this role earn between $26.20 and $48.80 per hour, depending on experience, location, and employer.

What is a medical device technical writer?

A Medical Device Technical Writer creates clear, accurate documentation for medical devices, including user manuals, regulatory submissions, and technical reports. They translate complex technical information into understandable content for various audiences, such as healthcare professionals, regulatory agencies, and end-users. This role requires knowledge of medical device regulations, engineering concepts, and technical writing standards. Strong attention to detail and collaboration with engineers, regulatory specialists, and subject matter experts are essential.

What are the typical day-to-day responsibilities of a medical device technical writer?

As a Medical Device Technical Writer, your daily responsibilities usually include creating and revising user manuals, product instructions, and regulatory documentation for medical devices. You'll often collaborate closely with subject matter experts such as engineers, product managers, and quality assurance teams to gather technical details and ensure accuracy. You may also be involved in reviewing documents for compliance with industry regulations and standards, as well as participating in document audits or updates. The role requires balancing multiple projects and deadlines while ensuring all materials are clear, concise, and suitable for their intended audience.

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

To thrive as a Medical Device Technical Writer, you need a deep understanding of medical terminology, regulatory standards, and technical writing best practices, typically supported by a degree in science, engineering, or technical communication. Familiarity with document management systems, authoring tools (such as Adobe FrameMaker or MadCap Flare), and knowledge of FDA or ISO documentation requirements are often essential. Exceptional attention to detail, strong organizational skills, and clear communication help writers collaborate effectively with engineers, clinicians, and regulatory teams. These skills and attributes ensure that complex medical device information is accurately documented, compliant with regulations, and accessible to diverse stakeholders.

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Infographic showing various Medical Device Technical Writer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 15% Part Time, and 7% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $80,364 per year, or $38.6 per hour.

$68K - $96K/yr

Full-time

Re-posted 17 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 540 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.

  • This is an onsite role based in Irvine, CA. Relocation assistance is not provided, and candidates must reside within a 50-mile radius of Irvine to 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.


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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