Stellar Consulting Solutions, LLC
Technical Writer
Stellar Consulting Solutions, LLC, San Diego, California, United States, 92189
Stellar Consulting Solutions, LLC provided pay range
This range is provided by Stellar Consulting Solutions, LLC. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $45.00/hr - $47.00/hr
Direct message the job poster from Stellar Consulting Solutions, LLC
The Senior Technical Writer develops, edits, and maintains technical documentation for
Class II medical devices . This role works closely with engineering, quality, regulatory, clinical, and marketing teams to ensure documentation is accurate, clear, user-friendly, and compliant with regulatory standards.
Key Responsibilities:
Write and maintain
user manuals, IFUs, installation guides, troubleshooting guides , and upgrade/downgrade instructions for global regulatory submissions
Ensure documentation meets
FDA and international regulatory requirements , industry standards, and internal policies
Create or support
illustrations, diagrams, flowcharts, tables, and images
to clearly explain technical information
Collaborate with
engineering, QA, regulatory, clinical, marketing, and customer support
teams to gather content and improve document clarity and usability
Review and edit documentation for
accuracy, consistency, and compliance
Develop and maintain
documentation standards, templates, and style guides
Manage multiple documentation projects, timelines, and priorities in a fast-paced environment
Lead or participate in
cross-functional meetings
related to documentation requirements
Mentor junior technical writers
Stay current on
regulatory updates and industry best practices.
Qualifications:
5+ years
of experience writing and editing
technical product documentation
(hardware/software)
Strong background in
regulatory compliance
for medical devices or pharmaceuticals
Experience with
device labeling and packaging content
Ability to work independently, manage multiple priorities, and meet tight deadlines
Familiarity with
electro-mechanical systems and software applications
Experience with
engineering change control
and Agile development preferred
Experience with
version control systems
(Git, Perforce, SVN, TFS)
Experience with
ERP systems
(SAP, Oracle) is a plus
Knowledge of
photo editing tools
(Adobe Photoshop)
Proficiency with
desktop publishing tools
(MadCap Flare, FrameMaker, InDesign, Illustrator, XML/DITA)
Skilled in both
electronic and hard-copy markup
(Word, Acrobat, tracked changes)
Kindly share resume at gaurav@stellarconsulting.com or call me at 678-935-7045 to discuss more!
Seniority level Associate
Employment type Contract
Industries Medical Equipment Manufacturing
#J-18808-Ljbffr
Base pay range $45.00/hr - $47.00/hr
Direct message the job poster from Stellar Consulting Solutions, LLC
The Senior Technical Writer develops, edits, and maintains technical documentation for
Class II medical devices . This role works closely with engineering, quality, regulatory, clinical, and marketing teams to ensure documentation is accurate, clear, user-friendly, and compliant with regulatory standards.
Key Responsibilities:
Write and maintain
user manuals, IFUs, installation guides, troubleshooting guides , and upgrade/downgrade instructions for global regulatory submissions
Ensure documentation meets
FDA and international regulatory requirements , industry standards, and internal policies
Create or support
illustrations, diagrams, flowcharts, tables, and images
to clearly explain technical information
Collaborate with
engineering, QA, regulatory, clinical, marketing, and customer support
teams to gather content and improve document clarity and usability
Review and edit documentation for
accuracy, consistency, and compliance
Develop and maintain
documentation standards, templates, and style guides
Manage multiple documentation projects, timelines, and priorities in a fast-paced environment
Lead or participate in
cross-functional meetings
related to documentation requirements
Mentor junior technical writers
Stay current on
regulatory updates and industry best practices.
Qualifications:
5+ years
of experience writing and editing
technical product documentation
(hardware/software)
Strong background in
regulatory compliance
for medical devices or pharmaceuticals
Experience with
device labeling and packaging content
Ability to work independently, manage multiple priorities, and meet tight deadlines
Familiarity with
electro-mechanical systems and software applications
Experience with
engineering change control
and Agile development preferred
Experience with
version control systems
(Git, Perforce, SVN, TFS)
Experience with
ERP systems
(SAP, Oracle) is a plus
Knowledge of
photo editing tools
(Adobe Photoshop)
Proficiency with
desktop publishing tools
(MadCap Flare, FrameMaker, InDesign, Illustrator, XML/DITA)
Skilled in both
electronic and hard-copy markup
(Word, Acrobat, tracked changes)
Kindly share resume at gaurav@stellarconsulting.com or call me at 678-935-7045 to discuss more!
Seniority level Associate
Employment type Contract
Industries Medical Equipment Manufacturing
#J-18808-Ljbffr