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Api Technical Writer Remote Jobs in Colorado (NOW HIRING)

Remote Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based ... Bachelor's degree in a scientific, technical, healthcare, or related discipline. * Minimum 6 years ...

New

API Engineer

Boulder, CO · On-site +1

$75K - $110K/yr

Testing & validation: write unit and integration tests and output-validation checks to confirm ... technical services. Our continually expanding team combines scientific expertise with mature ...

Testing & validation: write unit and integration tests and output-validation checks to confirm ... technical services. Our continually expanding team combines scientific expertise with mature ...

Excellent written and verbal communication skills. * Proven ability to manage multiple priorities ... Remote work model #LI-REMOTE * Competitive benefits package and competitive total compensation * An ...

Excellent written and verbal communication skills. * Proven ability to manage multiple priorities ... Remote work model #LI-REMOTE * Competitive benefits package and competitive total compensation * An ...

Excellent written and verbal communication skills. * Proven ability to manage multiple priorities ... Remote work model #LI-REMOTE * Competitive benefits package and competitive total compensation * An ...

Technical Editor, Mid

Aurora, CO · On-site +1

$61K - $141K/yr

Remote Work: No Job Number: R0247075 Location: Aurora,CO,US Share job via: Share Technical Editor ... You Have: * 3+ years of experience reviewing written intelligence products for grammar, punctuation ...

This is a full-time, remote position. We do expect the successful candidate to come to the Denver ... Write technical specs, document common components, and keep the team accountable for necessary ...

Collaborate with stakeholders to gather requirements and translate business needs into technical ... Experience building and supporting REST API integrations within ServiceNow (required) Experience ...

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Api Technical Writer Remote information

What is an API technical writer?

An API Technical Writer (Remote) is a professional who creates clear, accurate, and user-friendly documentation for Application Programming Interfaces (APIs) while working from a remote location. Their role involves collaborating with developers and product teams to understand how APIs work, and then producing guides, reference materials, and tutorials for developers who use the API. They help ensure that API documentation is comprehensive and easy to understand, which is crucial for developers integrating with the API. Remote API technical writers use various tools and platforms to communicate and deliver their work, making strong communication and self-management skills essential for this role.

How does an API technical writer typically collaborate with developers and product teams in a remote work environment?

As a remote API Technical Writer, you'll frequently collaborate with developers, product managers, and QA engineers using tools like Slack, Jira, and video conferencing platforms. Regular communication is essential to clarify technical concepts, gather up-to-date information about new or changing APIs, and ensure documentation aligns with product releases. You may participate in virtual sprint meetings, review sessions, and asynchronous feedback cycles to keep documentation accurate and user-friendly. Developing strong relationships and proactive communication habits are key to overcoming the challenges of remote collaboration in this highly cross-functional role.

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

To thrive as an API Technical Writer (Remote), you need strong technical writing abilities, a solid understanding of software development concepts, and experience with API documentation standards, often supported by a degree in English, Computer Science, or a related field. Familiarity with tools like Swagger/OpenAPI, Markdown, Git, and content management systems, as well as knowledge of RESTful APIs, is typically required. Excellent communication, attention to detail, and the ability to collaborate virtually with developers and stakeholders are standout soft skills. These skills are crucial to producing clear, accurate documentation that enables users and developers to efficiently integrate and use APIs.

What are the most commonly searched types of Api Technical Writer jobs in Colorado?

The most popular types of Api Technical Writer jobs in Colorado are:

What cities in Colorado are hiring for Api Technical Writer Remote jobs?

Cities in Colorado with the most Api Technical Writer Remote job openings:

Infographic showing various Api Technical Writer Remote job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 87% Full Time, 8% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution.

Senior Staff Medical Writer (Remote)

Stryker

Denver, CO • On-site, Remote

$143K - $238K/yr

Full-time

Posted 3 days ago

New


Stryker rating

8.2

Company rating: 8.2 out of 10

Based on 112 frontline employees who took The Breakroom Quiz

132nd of 491 rated machine equipment manufacturers


Job description

Work Flexibility: Remote

Stryker is hiring a Senior Staff Medical Writer to join our Endoscopy Division, to be based remotely anywhere within the United States. Stryker is one of the world's leading medical technology companies and, together with its customers, is driven to make healthcare better. Our Endoscopy Division delivers a diverse array of innovative medical technologies to support minimal invasive surgery through brilliant visualization, connected OR solutions, sports medicine products to sustainability solutions.

As the Senior Staff Medical Writer, you will develop scientific and clinical documentation that supports global regulatory compliance and market access for medical devices. This position partners closely with Regulatory Affairs, Clinical Affairs, Quality, Research & Development, and Marketing teams to translate complex clinical evidence into high-quality regulatory and scientific documents throughout the product lifecycle.

What You Will Do

  • Author and maintain Clinical Evaluation Reports (CERs), Post-Market Clinical Follow-Up (PMCF) documents, and other clinical evidence documentation supporting international product registrations and lifecycle management.

  • Compile, analyze, and synthesize clinical evidence from clinical studies, published literature, post-market data, and other safety and performance sources into submission-ready regulatory documents.

  • Respond to notified body reviews and regulatory feedback, driving resolution of clinical documentation questions to support ongoing market access.

  • Collaborate with cross-functional teams to develop clinical evidence strategies, regulatory documentation plans, and project timelines.

  • Author clinical study protocols, study reports, data summaries, and supporting scientific documents for regulatory and clinical initiatives.

  • Conduct systematic literature reviews, evaluate scientific data, and integrate findings into clinical and regulatory documentation.

  • Lead document review cycles, coordinate stakeholder feedback, resolve content issues, and obtain timely approvals.

  • Drive continuous improvement initiatives, maintain medical writing tools and templates, and mentor junior medical writing team members.

What You Need

Required

  • Bachelor's degree in a scientific, technical, healthcare, or related discipline.

  • Minimum 6 years of industry experience within medical technology, medical devices, pharmaceuticals, or healthcare products.

  • Minimum 4 years of experience in scientific writing, medical writing, clinical research, or related regulatory documentation activities.

  • Experience authoring Clinical Evaluation Reports (CERs) and Post-Market Clinical Follow-Up (PMCF) documentation.

  • Expert knowledge of MEDDEV 2.7/1 Rev. 4, European Union Medical Device Regulation (EU MDR 2017/745), and Medical Device Coordination Group (MDCG) guidance for clinical evaluations.

  • Experience conducting systematic literature reviews and utilizing scientific databases, literature search methodologies, and literature management tools.

  • Knowledge of FDA, Good Clinical Practice (GCP), ISO 14155, ISO 14971, and applicable international medical device regulations and standards.

Preferred

  • Master's degree, PhD, PharmD, MD, MPH, RN, BSN, or other advanced health-related degree.

  • Experience authoring clinical study protocols, clinical study reports, manuscripts, or scientific publications.

  • Experience supporting regulatory submissions and global market access initiatives for medical devices.

  • Knowledge of clinical operations, risk management, and international regulatory requirements.

United States of America Pay Ranges:

  • USN: $110,100 - $183,400 USD Annual
  • US5: $115,600 - $192,600 USD Annual
  • US10: $121,100 - $201,700 USD Annual
  • US15: $126,600 - $210,900 USD Annual
  • US20: $132,100 - $220,100 USD Annual
  • US30: $143,100 - $238,400 USD Annual
View the U.S. work location and transparency guide to find the pay range for your location.

Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.

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