DGN Technologies
Overview
Be among the first 25 applicants. Hiring: Technical Writer 3 | Sunnyvale, CA (Onsite at 1020 Kifer Rd). Pay Rate: Up to $65/hr (W2). We’re seeking an experienced
Technical Writer
with a background in creating
user-facing documentation
(user manuals, IFUs) for regulated industries such as
medical devices, automotive, or aviation . Responsibilities
5+ years of
technical writing
experience focused on
end-user documentation
(not internal SOPs). Proficient with
DITA ,
Oxygen ,
Arbortext ,
XML , or similar authoring tools. Experience in regulated industries – able to incorporate warnings, cautions, and compliance requirements. Skilled in
Adobe FrameMaker ,
InDesign , and
Acrobat . Strong writing, editing, and content validation abilities. Develop accurate, compliant
Instructions for Use (IFUs)
for medical device systems and instruments. Collaborate with engineers, designers, and SMEs to produce clear and consistent documentation. Ensure deliverables align with
FDA and regulatory guidelines . Participate in content validation, verification, and document control processes. Qualifications
Experience creating user-facing documentation for regulated industries (medical devices, automotive, or aviation). Ability to work onsite in Sunnyvale, CA. Strong communication and cross-functional collaboration skills. Demonstrated track record of producing compliant, user-friendly documentation. Job Details
Seniority level:
Mid-Senior level Employment type:
Contract Job function:
Marketing, Public Relations, and Writing/Editing Industries:
IT Services and IT Consulting
#J-18808-Ljbffr
Be among the first 25 applicants. Hiring: Technical Writer 3 | Sunnyvale, CA (Onsite at 1020 Kifer Rd). Pay Rate: Up to $65/hr (W2). We’re seeking an experienced
Technical Writer
with a background in creating
user-facing documentation
(user manuals, IFUs) for regulated industries such as
medical devices, automotive, or aviation . Responsibilities
5+ years of
technical writing
experience focused on
end-user documentation
(not internal SOPs). Proficient with
DITA ,
Oxygen ,
Arbortext ,
XML , or similar authoring tools. Experience in regulated industries – able to incorporate warnings, cautions, and compliance requirements. Skilled in
Adobe FrameMaker ,
InDesign , and
Acrobat . Strong writing, editing, and content validation abilities. Develop accurate, compliant
Instructions for Use (IFUs)
for medical device systems and instruments. Collaborate with engineers, designers, and SMEs to produce clear and consistent documentation. Ensure deliverables align with
FDA and regulatory guidelines . Participate in content validation, verification, and document control processes. Qualifications
Experience creating user-facing documentation for regulated industries (medical devices, automotive, or aviation). Ability to work onsite in Sunnyvale, CA. Strong communication and cross-functional collaboration skills. Demonstrated track record of producing compliant, user-friendly documentation. Job Details
Seniority level:
Mid-Senior level Employment type:
Contract Job function:
Marketing, Public Relations, and Writing/Editing Industries:
IT Services and IT Consulting
#J-18808-Ljbffr