Senior Technical Writer w/Madcap FLARE
Mastech Inc. - Marlborough, Massachusetts, us, 01752![Mastech Inc.](/api/image?src=https%3A%2F%2Fgeneral-board-default.s3.us-east-2.amazonaws.com%2Fpublic%2Fimages%2Fdesk-360x180.webp&w=640&q=75&f=webp)
Work at Mastech Inc.
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Overview
All the relevant skills, qualifications and experience that a successful applicant will need are listed in the following description.Mastech Digital
provides digital and mainstream technology staff as well as Digital Transformation Services for all American Corporations. We are currently seeking a
Technical Writer with Madcap FLARE
for our client in the
Pharmaceutical
domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a
Contract
position, and the client is looking for someone to start immediately.Location:
Marlborough, MARole:
Technical Writer with Madcap FLAREPrimary Skills:
MadCap FlareRole Description:
The
Technical Writer with Madcap FLARE
must have at least 5+ years of experience. For this role, you must have experience with MadCap Flare software.The Technical Writer is responsible for the generation and maintenance of written technical matter supporting product lines. This role involves working in conjunction with the Technical Service, Product Development and other departments to research, plan and produce a variety of technical material for Medical Device products.These include Operator and Service Manuals, Quick Reference Guides, Package Inserts, Specification Sheets, Labeling, Technical Bulletins, etc.Responsibilities:Generate written text, document formatting, create and procure technical artwork, coordinates projects through to final print and or electronic distribution.Solicit training and feedback from in-house technical expert project managers, engineers, application specialists, etc. to help with design and development of technical documentation.Support Training efforts in house and remote to validate new and or revised documentation.Update and maintain existing technical publications as needed.Execute necessary Change Orders or other quality system processes while maintaining regulatory compliance.Coordinates and implements translations of technical written matter for Medical Device products into required local languages as needed.Support the electronic and hardcopy libraries of released and archived material.Education:
Bachelor’s degree in Computer Science, Electrical/Electronic Engineering, Information Technology or another related field or Equivalent.Experience:
Minimum 5+ years of experience.Relocation:
This position will not cover relocation expenses.Travel:
No.Local Preferred:
Yes.Note:
Must be able to work on a W2 basis (No C2C).
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