Technical Writer
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
Irvine, CA · On-site
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
Irvine, CA · On-site
$68K - $96K/yr
As a Technical Writer, you own well-scoped controlled documentation that keeps our regulated ... Biotechnology, medical device, or regulated industry experience, or equivalent work experience ...
The Technical Writer/Analyst Medical Affairs, Business Process & Operations will support the file ... Medical Device (MD) operating companies. * This person will collaborate with Medical Affairs ...
The Technical Writer/Analyst Medical Affairs, Business Process & Operations will support the file ... Medical Device (MD) operating companies. * This person will collaborate with Medical Affairs ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Morrisville, NC · On-site
$55.10 - $110.21/hr
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Morrisville, NC · On-site
$55.10 - $110.21/hr
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
Senior level 8-15 years of experience in technical writing within the Pharma, Medical Device, or BioTech industries is desired. Desired Aptitude and Skill Set: * Resourceful * Extremely detail ...
$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 ...
$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 ...
$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 ...
$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 ...
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 ...
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 ...
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 ...
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 ...
San Diego, CA · On-site
$90 - $130/hr
Overview Technical Writer job at Stellar Consulting Solutions, LLC. San Diego, CA. Location: San ... The ideal candidate will have extensive experience in the medical device industry and the ability ...
New
San Diego, CA · On-site
$90 - $130/hr
Overview Technical Writer job at Stellar Consulting Solutions, LLC. San Diego, CA. Location: San ... The ideal candidate will have extensive experience in the medical device industry and the ability ...
New
Mountain View, CA · On-site
$60 - $65/hr
Job Title: Technical Writer Location: Mountain View, CA 94043 Duration: 12 Months * Produce ... Plan, write, and edit instructions for use (IFU) for medical device systems and instruments ...
Quick apply
Mountain View, CA · On-site
$60 - $65/hr
Job Title: Technical Writer Location: Mountain View, CA 94043 Duration: 12 Months * Produce ... Plan, write, and edit instructions for use (IFU) for medical device systems and instruments ...
Raritan, NJ · On-site
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 ...
Raritan, NJ · On-site
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 ...
$60 - $70/hr
Technical Writer (FDA/GMP Documentation) Location: Petaluma, CA (100% Onsite) Pay: $60 - $70/hour ... Experience supporting pharmaceutical, biotechnology, medical device, food manufacturing, or similar ...
Quick apply
$60 - $70/hr
Technical Writer (FDA/GMP Documentation) Location: Petaluma, CA (100% Onsite) Pay: $60 - $70/hour ... Experience supporting pharmaceutical, biotechnology, medical device, food manufacturing, or similar ...
Chicago, IL · Hybrid
$150K - $210K/yr
... medical device technical execution. You will partner closely with R&D, Product Management ... Excellent written and verbal communication skills, including the ability to act as translator among ...
Chicago, IL · Hybrid
$150K - $210K/yr
... medical device technical execution. You will partner closely with R&D, Product Management ... Excellent written and verbal communication skills, including the ability to act as translator among ...
Chicago, IL · On-site
$150K - $210K/yr
... medical device technical execution. You will partner closely with R&D, Product Management ... Excellent written and verbal communication skills, including the ability to act as translator among ...
Chicago, IL · On-site
$150K - $210K/yr
... medical device technical execution. You will partner closely with R&D, Product Management ... Excellent written and verbal communication skills, including the ability to act as translator among ...
Chicago, IL · On-site
$150K - $210K/yr
... medical device technical execution. You will partner closely with R&D, Product Management ... Excellent written and verbal communication skills, including the ability to act as translator among ...
Chicago, IL · On-site
$150K - $210K/yr
... medical device technical execution. You will partner closely with R&D, Product Management ... Excellent written and verbal communication skills, including the ability to act as translator among ...
Collaborating with remote global teams, including device, application, test, etc. to innovate new technologies with maximum development efficiency. Technical Writer Mandatory Skills * BA/BS degree or ...
Collaborating with remote global teams, including device, application, test, etc. to innovate new technologies with maximum development efficiency. Technical Writer Mandatory Skills * BA/BS degree or ...
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 ...
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 ...
$14.18 - $18.16
3% of jobs
$18.16 - $22.14
9% of jobs
$26.03 is the 25th percentile. Wages below this are outliers.
$22.14 - $26.11
13% of jobs
$26.11 - $30.09
7% of jobs
$30.09 - $34.07
8% of jobs
$34.07 - $38.05
5% of jobs
The median wage is $39.79 / hr.
$38.05 - $42.02
8% of jobs
$42.02 - $46
16% of jobs
$47.54 is the 75th percentile. Wages above this are outliers.
$46 - $49.98
12% of jobs
$49.98 - $53.96
7% of jobs
$53.96 - $57.93
11% of jobs
$14
$38
$57
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.
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.
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.
Cities with the most Medical Device Technical Writer job openings:
The most popular types of Medical Device Technical Writer jobs are:
States with the most job openings for Medical Device Technical Writer jobs include:
The top searched job categories for Medical Device Technical Writer jobs are:

$68K - $96K/yr
Full-time
Re-posted 17 days ago
8.3
Based on 30 frontline employees who took The Breakroom Quiz
68th of 540 rated manufacturers
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 ImpactCreate 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.
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.
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.
Get the full story on Breakroom
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.
Medical equipment and supplies manufacturing
10,000+ Employees
Irvine, CA, US
1958