LinkedIn - Jobboard
Technical Writer W/ Documentation [Need Global experience] - REMOTE - Urgent Nee
LinkedIn - Jobboard, Franklin Lakes, New Jersey, us, 07417
Position:
Technical Writer W/ Documentation [Need Global experience] - REMOTELocation:
RemoteDuration:
3+ Months ContractTotal Hours/week:
40.00Shift:
1st ShiftClient:
Medical Device CompanyEmployment Type:
Contract on W2 (Need US Citizens Or GC Holders Only)No H1B’sJob Description We are looking for a Technical Writer to produce high-quality global policies and procedures to be used across all Client sites, businesses, and regions. The writer will work with the Global Process Owner and development teams to define the process and then outline the process according to standardized formats and structure. Additionally, the role will support the document management process.Position Responsibilities
Develop, manage, and execute a documentation project from initiation through delivery.Analyze the request, create draft documents in active voice, and revise according to feedback.Create global policies, procedures, work instructions, forms, and technical standards based on input from GPO and process teams using templates and style guides.Partner with GPOs and teams to ensure that procedures accurately reflect the desired end state process.Estimated 85% original writing/15% revisions.Provide support to the document control team for the release of global documents.Prepare document package for routing and approval in the electronic document management system.Process document package in e-DMS.Job Requirements
Will involve conducting remote live video meetings with various corporate employees.Proven experience working in a technical writing position.Experience in writing documentation for the medical device industry according to the Quality Systems Regulation and/or ISO 13485 is required.Ability to deliver high-quality documentation paying close attention to detail.Ability to quickly grasp complex technical concepts and make them easily understandable in text and pictures.Excellent written skills in English - Writing samples may be required upon request.Strong working knowledge of Microsoft Office Suite.Experience working with electronic documents management systems.BA/BS required with 2 years of business experience, or without BA/BS degree, 5+ years extensive experience in the applicable area.
You could be just the right applicant for this job Read all associated information and make sure to apply.#J-18808-LjbffrRemote working/work at home options are available for this role.
Technical Writer W/ Documentation [Need Global experience] - REMOTELocation:
RemoteDuration:
3+ Months ContractTotal Hours/week:
40.00Shift:
1st ShiftClient:
Medical Device CompanyEmployment Type:
Contract on W2 (Need US Citizens Or GC Holders Only)No H1B’sJob Description We are looking for a Technical Writer to produce high-quality global policies and procedures to be used across all Client sites, businesses, and regions. The writer will work with the Global Process Owner and development teams to define the process and then outline the process according to standardized formats and structure. Additionally, the role will support the document management process.Position Responsibilities
Develop, manage, and execute a documentation project from initiation through delivery.Analyze the request, create draft documents in active voice, and revise according to feedback.Create global policies, procedures, work instructions, forms, and technical standards based on input from GPO and process teams using templates and style guides.Partner with GPOs and teams to ensure that procedures accurately reflect the desired end state process.Estimated 85% original writing/15% revisions.Provide support to the document control team for the release of global documents.Prepare document package for routing and approval in the electronic document management system.Process document package in e-DMS.Job Requirements
Will involve conducting remote live video meetings with various corporate employees.Proven experience working in a technical writing position.Experience in writing documentation for the medical device industry according to the Quality Systems Regulation and/or ISO 13485 is required.Ability to deliver high-quality documentation paying close attention to detail.Ability to quickly grasp complex technical concepts and make them easily understandable in text and pictures.Excellent written skills in English - Writing samples may be required upon request.Strong working knowledge of Microsoft Office Suite.Experience working with electronic documents management systems.BA/BS required with 2 years of business experience, or without BA/BS degree, 5+ years extensive experience in the applicable area.
You could be just the right applicant for this job Read all associated information and make sure to apply.#J-18808-LjbffrRemote working/work at home options are available for this role.