Technical Writer I

Remote in Irvine, CA, US • Posted 11 hours ago • Updated 11 hours ago

Contract W2

On-site

Fitment

Dice Job Match Score™

📋 Comparing job requirements...

Job Details

Skills

Science
Editing
Research
Scripting
Lifecycle Management
Management
Workflow
Regulatory Compliance
Collaboration
Manufacturing
Research and Development
Documentation
Continuous Improvement
WIS
Technical Writing
Medical Devices
Microsoft Office
Microsoft Excel
Microsoft PowerPoint
Plant Lifecycle Management
Product Lifecycle Management
Document Management
Analytical Skill
Root Cause Analysis
Problem Solving
Conflict Resolution
Reporting
Communication
Attention To Detail

Summary

Kelly Science and Clinical FSP is currently seeking a Technical Writer I for a long-term engagement in Irvine, CA with one of our Global Medical Device clients. This position is hybrid. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you may be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to choose from. You may also be eligible for paid time off, including holiday, vacation, and sick/personal time.
We are looking for a detail-oriented Technical Writer to bridge the gap between complex engineering concepts and clear, compliant documentation. You will work directly with our Scientific and Engineering teams to document research findings, create technical manuals, and manage the Engineering Change Order (ECO) process. In this role, you aren't just a writer-you are a guardian of accuracy and traceability in a high-stakes medical device environment.
Key Responsibilities

Technical Documentation: Write and edit high-level research reports, technical manuals, specifications, and regulatory scripts.
Information Synthesis: Transform complex data into clear abstracts, summaries, charts, and graphs tailored for both technical and non-technical audiences.
Lifecycle Management: Manage the workflow for Change Requests and ECOs, ensuring 100% traceability and compliance with industry standards.
Standardization: Develop and maintain document templates, naming conventions, and numbering standards to ensure a unified "source of truth."
Cross-Functional Collaboration: Partner with Manufacturing, R&D, and Quality teams to ensure documentation aligns with production schedules and safety regulations.
Continuous Improvement: Identify and retire obsolete procedures (WIs) and look for ways to streamline the document approval process.

What You Bring (Requirements)

Education: Bachelor's Degree in Technical Writing, Communications, Engineering, or a related field.
Experience: Minimum of 2 years in technical writing; Medical Device industry experience is strongly preferred.
Tech Stack: Proficiency in MS Office Suite (Word, Excel, PowerPoint). Experience with PLM or Document Control software is a major plus.
Analytical Mindset: Strong root-cause analysis and problem-solving skills. You don't just report a problem; you help document the solution.
Communication: Exceptional written and verbal skills with the ability to "interview" engineers to extract technical details.
Precision: Attention to detail and a "quality-first" mindset.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 10105282
Position Id: 869522
Posted 11 hours ago

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

Technical Writer I

Michigan

•

Today

Job Title: Technical Writer Location: Hemlock, MI 48626 Duration: 6+ Months Job Type: Contract Top Required Skills: Technical documentation development Cross-functional collaboration Clear, user-focused technical writing Must-Have Skills: Experience developing and maintaining technical documentation (process manuals, system specs, guidelines, procedures) Ability to translate complex technical concepts into clear, user-friendly content Strong written and verbal communication skills Proficienc

Contract

CMC Regulatory Technical Writer

Remote

•

Today

Degree in Pharmacy or a relevant science/technical subject such as chemistry, biology, or related field.Minimum of 10 years within a CMC role in the pharmaceutical industry, with at least 5 years being directly involved with a CMC regulatory submission technical writing role.Significant knowledge of CMC-related regulatory requirements and guidelines (e.g., ICH, FDA, EMA) and experience with eCTD submissions.Exceptional technical writing skills with the ability to communicate complex scientific i

Easy Apply

Contract

$50 - $60

Technical Writer - Clearance Required

Remote

•

Today

Overview LMI seeks an experienced Technical Writer to support the U.S. Army's Holistic Health & Fitness (H2F) initiative as a member of the User Engagement functional team within the H2F Program Support Team. The Technical Writer is responsible for developing clear, accurate, and user-focused written content that communicates Government-approved strategies, guidance, and analytic insights delivered through the Holistic Health and Fitness Management System (H2FMS). This role focuses on content

Contract

USD 80,000.00 - 125,000.00 per year

Technical Writer

Remote

•

25d ago

The Tri-Com Consulting Group is a Full-Service IT Employment Consulting Firmwho is seeking qualified candidates for the following opening: Technical Writer Title: Technical Writer Duration: March March 2027 Work Site: Remote Scope of Work The Technical Writer will collaborate with the staff and a Data Analyst to begin the planning and implementation of a statewide community health needs assessment that identifies the communities with the greatest unmet health care needs, disparities in health o

Easy Apply

Third Party, Contract

Depends on Experience

Search all similar jobs