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 ...
Sr. Manager, Medical Device Cyber Security
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 ...
Sr. Manager, Medical Device Cyber Security
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 ...
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Engineering Technical Writer
Clearwater, FL · On-site
$60K - $70K/yr
Minimum of 2-4 years of experience in technical writing within a regulated industry, preferably in medical device manufacturing. • Strong understanding of documentation requirements for FDA ...
Quick apply
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Engineering Technical Writer
Clearwater, FL · On-site
$60K - $70K/yr
Minimum of 2-4 years of experience in technical writing within a regulated industry, preferably in medical device manufacturing. • Strong understanding of documentation requirements for FDA ...
DITA XML Technical Writer
Sunnyvale, CA · Hybrid
$78/hr
Plans, writes, edits, and maintains Field Service documentation (i.e., Field Service procedures and technical bulletins) for medical device systems. * Complete documentation control steps to release ...
DITA XML Technical Writer
Sunnyvale, CA · Hybrid
$78/hr
Plans, writes, edits, and maintains Field Service documentation (i.e., Field Service procedures and technical bulletins) for medical device systems. * Complete documentation control steps to release ...
Medical Device Technical Program Coordinator Are you a Medical Device Technical Program Coordinator ... Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of ...
New
Medical Device Technical Program Coordinator Are you a Medical Device Technical Program Coordinator ... Under the San Francisco Lactation in the Workplace Ordinance, we will provide written notice of ...
New
SOP Specialist / Technical Writer (Training & Documentation)-Medical Devices
Rensselaer, NY · On-site
$40/hr
SOP Specialist / Technical Writer (Training & Documentation) Location: Rensselaer, NY Employment ... pharma/medical device industries * Strong understanding of cGMP, FDA, and/or ISO regulations
Quick apply
SOP Specialist / Technical Writer (Training & Documentation)-Medical Devices
Rensselaer, NY · On-site
$40/hr
SOP Specialist / Technical Writer (Training & Documentation) Location: Rensselaer, NY Employment ... pharma/medical device industries * Strong understanding of cGMP, FDA, and/or ISO regulations
Technical Writer
Sunnyvale, CA · On-site
$73 - $78/hr
Plans, writes, edits, and maintains Field Service documentation (i.e., Field Service procedures and technical bulletins) for medical device systems. * Complete documentation control steps to release ...
Quick apply
Technical Writer
Sunnyvale, CA · On-site
$73 - $78/hr
Plans, writes, edits, and maintains Field Service documentation (i.e., Field Service procedures and technical bulletins) for medical device systems. * Complete documentation control steps to release ...
Sr. Manager, Medical Device Cyber Security
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 ...
Sr. Manager, Medical Device Cyber Security
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 ...
Required : • 3+ years of technical writing experience in a GxP-regulated pharmaceutical, biotech, or medical device environment • Proven experience authoring IQ/OQ/PQ protocols, SOPs, and RTMs in ...
Required : • 3+ years of technical writing experience in a GxP-regulated pharmaceutical, biotech, or medical device environment • Proven experience authoring IQ/OQ/PQ protocols, SOPs, and RTMs in ...
Sr. Manager, Medical Device Cyber Security
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 ...
Sr. Manager, Medical Device Cyber Security
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 ...
Technical Writer in Mountain View, CA 94043
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 ...
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Technical Writer in Mountain View, CA 94043
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 ...
Kforce has a client that is seeking a Technical Writer in Acton, MA. Overview: The UX Instructional ... medical device experience preferred * Ability to understand and communicate complex medical ...
Kforce has a client that is seeking a Technical Writer in Acton, MA. Overview: The UX Instructional ... medical device experience preferred * Ability to understand and communicate complex medical ...
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 ...
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 ...
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 ...
New
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 ...
New
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 ...
New
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 ...
New
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 ...
New
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 ...
New
Engineering - Technical Writer - Exempt
North Haven, CT · On-site
$45 - $50/hr
Key Responsibilities * Plan, research, develop, and write medical device labeling, managing ... Conduct interviews with various users and technical staff to gather data for documentation.
Engineering - Technical Writer - Exempt
North Haven, CT · On-site
$45 - $50/hr
Key Responsibilities * Plan, research, develop, and write medical device labeling, managing ... Conduct interviews with various users and technical staff to gather data for documentation.
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 ...
New
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 ...
New
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 ...
Medical Device Technical Writer information
See salary details
$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
How much do medical device technical writer jobs pay per hour?
As of Jun 14, 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 are the key skills and qualifications needed to thrive in the Medical Device Technical Writer position, and why are they important?
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.
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 is a Medical Device Technical Writer job?
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.
More about Medical Device Technical Writer jobs
What cities are hiring for Medical Device Technical Writer jobs? Cities with the most Medical Device Technical Writer job openings:
What are the most commonly searched types of Medical Device Technical Writer jobs? The most popular types of Medical Device Technical Writer jobs are:
What states have the most Medical Device Technical Writer jobs? States with the most job openings for Medical Device Technical Writer jobs include:
What job categories do people searching Medical Device Technical Writer jobs look for? The top searched job categories for Medical Device Technical Writer jobs are:
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
Responsibilities:
- The Technical Writer/Analyst Medical Affairs, Business Process & Operations will support the file standardization for a new controlled document management system.
- S/He gathers documents, compiles information, and maintains records for creation of Medical Affairs internal documents.
- Reviews documents for accuracy and elevates issues to supervisor.
- This person will participate in change management activities relating to harmonizing Medical Operations processes across the Medical Device (MD) operating companies.
- This person will collaborate with Medical Affairs associates to help ensure that Medical Affairs' documents align with the global cross-functional strategy.
- The candidate will be an experienced professional with a focus on creating forms, templates, data entry and organizing files in structured folders and SharePoint sites.
- This candidate shall also have experience creating training guides and Work Instructions.
- This person shall possess strong editorial skills including a good understanding of medical terminology and scientific publication bibliographic material.
- The successful candidate will contribute to dictionary of terms for understanding the hierarchy of products, disease states and specialties to build the smart search tools.
- This requires an understanding of medical terminology and evaluating synonymous keywords.
- This person shall support the Medical Affairs SharePoint team site creation and maintenance.
- This includes creating and assigning User Groups and Permissions, SharePoint Lists and Libraries.
- S/He will support medical operations cross-functionally within a matrix organization of medical device companies.
Qualifications
Qualifications:
- A Bachelor's Degree with 6+ years of related medical/ healthcare industry experience is required.
- Experience with MS Office applications (Word, SharePoint Online/2013, Outlook, Excel) is required.
- Ability to synthesize and understand search terms to create dictionary lists.
- Demonstrated knowledge and experience with medical terminology and medical device products in regulatory compliance or healthcare compliance is preferred.
- Strong typing and MS Office365 and SharePoint skills are required.
- Previous experience managing short deadlines, working with colleagues in different time zones and countries is required. The ability to work with people in a matrixed organization is highly preferred.
- This position will be located in Somerville, NJ and will require 0% travel.
Additional Information
Kind Regards,
Sasha Sharma
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
DIRECT # - 732-662-7964
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