• Snapboard
  • Activity
  • Reports
  • Campaign
Welcome ,

Chat with the recruiter

...Minimize

Hey I'm Online! Leave me a message.
Let me know if you have any questions.

Technical Writer/Editor 3

In Massachusetts / United States

Save this job

Technical Writer/Editor 3   

Click on the below icons to share this job to Linkedin, Twitter!

JOB TITLE:

Technical Writer/Editor 3

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Norwood Massachusetts / United States

JOB DESCRIPTION:

For this role at our client, assignment is contingent upon the Employer of Record’s receipt of sufficient proof that you are fully vaccinated against COVID-19 (meaning two weeks have passed after the last injection of Pfizer/Moderna or two weeks after receipt of the J&J). In some locations, testing for COVID-19 may be available and/or required. Requests for accommodation will be considered pursuant to applicable law.

Shift Start and End Time: 8 AM - 5 PM

The Sr. Tech Writer is responsible for researching, recommending, and developing labeling content and documentation that delivers optimal usability and efficiency for best-in-class information solutions for our customers.
In addition, a Sr. Tech Writer contributes to the development and achievement of organizational goals and objectives, may develop new programs and or processes as well as modifying and enhancing existing processes and or programs, and may act as a mentor for other Information Developers. This role reports to the Director of UXD and Product Labeling.

Responsibilities
•Develop high-quality medical device (Point of Care) product labeling & documentation content for a diverse audience, including end users, system administrators, and medical professionals.
•Produce technically precise and well-written content for use in online help, user guides, Quick Start Guides, IFUs, and other labeling documentation to support POC products.
•Work with product managers, engineers, regulatory, Marketing and other cross functional staff to gather content; proactively engage with subject matter experts.
•Manage multiple labeling and documentation projects to ensure delivery on schedule meeting our quality standards working with team members both within the product labeling team and across the organization.
•Actively seeks customer input, and may take responsibility for customer situations (internal and external customers).
•Exercises considerable latitude in determining technical objectives independently.
•Manage portions of internationalization/localization projects with outside vendors.
•Understands business and technical drivers and can balance both when making decisions.
•Understands team tools and minimalist writing style.
•Other duties as assigned.

Qualifications
•BA or BS or equivalent in Information Design, Computer Science or similar field.
•Excellent written and verbal communication skills.
•Experience documenting software, hardware, or technical content in medical device industry
•7+ years’ technical writing and content development experience, preferably in a medical device company.
•Excellent time & project management skills to multitask across multiple simultaneous projects.
•Thorough knowledge of Adobe products (FrameMaker, RoboHelp, Acrobat, InDesign) Microsoft Office, screen/image capture software.
•Quick learner and a team player with a proven ability to multi-task in a fast-paced environment.
•Proactive, helpful attitude, willing to jump in and help as needed.
•Strong interpersonal and communications skills.
•Experience working as a member of a high-performing team.
•Strong written and oral communication skills.
•Proven ability to create and implement a project plan.
•Ability to prioritize and focus on what's of highest value to customers.
•Collaborative leadership style.
•People skills to work with and obtain information from a wide variety of team members.
•Demonstrated problem-solving skills.
•Self-starter ability to quickly learn new tools and products.

Position Details

POSTED:

Sep 03, 2022

EMPLOYMENT:

INDUSTRY:

SNAPRECRUIT ID:

S1657184408083690

LOCATION:

Massachusetts / United States

CITY:

Norwood

Job Origin:

Jobsrus_organic_feed

A job sourcing event
In Dallas Fort Worth
Aug 19, 2017 9am-6pm
All job seekers welcome!

Technical Writer/Editor 3    Apply

Click on the below icons to share this job to Linkedin, Twitter!

For this role at our client, assignment is contingent upon the Employer of Record’s receipt of sufficient proof that you are fully vaccinated against COVID-19 (meaning two weeks have passed after the last injection of Pfizer/Moderna or two weeks after receipt of the J&J). In some locations, testing for COVID-19 may be available and/or required. Requests for accommodation will be considered pursuant to applicable law.

Shift Start and End Time: 8 AM - 5 PM

The Sr. Tech Writer is responsible for researching, recommending, and developing labeling content and documentation that delivers optimal usability and efficiency for best-in-class information solutions for our customers.
In addition, a Sr. Tech Writer contributes to the development and achievement of organizational goals and objectives, may develop new programs and or processes as well as modifying and enhancing existing processes and or programs, and may act as a mentor for other Information Developers. This role reports to the Director of UXD and Product Labeling.

Responsibilities
•Develop high-quality medical device (Point of Care) product labeling & documentation content for a diverse audience, including end users, system administrators, and medical professionals.
•Produce technically precise and well-written content for use in online help, user guides, Quick Start Guides, IFUs, and other labeling documentation to support POC products.
•Work with product managers, engineers, regulatory, Marketing and other cross functional staff to gather content; proactively engage with subject matter experts.
•Manage multiple labeling and documentation projects to ensure delivery on schedule meeting our quality standards working with team members both within the product labeling team and across the organization.
•Actively seeks customer input, and may take responsibility for customer situations (internal and external customers).
•Exercises considerable latitude in determining technical objectives independently.
•Manage portions of internationalization/localization projects with outside vendors.
•Understands business and technical drivers and can balance both when making decisions.
•Understands team tools and minimalist writing style.
•Other duties as assigned.

Qualifications
•BA or BS or equivalent in Information Design, Computer Science or similar field.
•Excellent written and verbal communication skills.
•Experience documenting software, hardware, or technical content in medical device industry
•7+ years’ technical writing and content development experience, preferably in a medical device company.
•Excellent time & project management skills to multitask across multiple simultaneous projects.
•Thorough knowledge of Adobe products (FrameMaker, RoboHelp, Acrobat, InDesign) Microsoft Office, screen/image capture software.
•Quick learner and a team player with a proven ability to multi-task in a fast-paced environment.
•Proactive, helpful attitude, willing to jump in and help as needed.
•Strong interpersonal and communications skills.
•Experience working as a member of a high-performing team.
•Strong written and oral communication skills.
•Proven ability to create and implement a project plan.
•Ability to prioritize and focus on what's of highest value to customers.
•Collaborative leadership style.
•People skills to work with and obtain information from a wide variety of team members.
•Demonstrated problem-solving skills.
•Self-starter ability to quickly learn new tools and products.


Please wait..!!