Bilingual Technical Writer - Raritan

A technical writer is required to have at least four years of experience on Azure. The role involves being an expert in various Azure services such as Virtual Machines and CosmosDB. · ResponsibilitiesCandidate should have at least 4 years of Azure experience · Knowledge and exper ...

+As part of the Portfolio Management Office within the AS Operations and Continuous Process Improvement organization, the Content Manager will curate and write content and communications to support key AS PMO programs and initiatives. · + · , ...

A top-rated technical writer with experience and background in the financial services systems is sought after. The candidate will work on documentation of technical applications that support our trading desks. · ...

A technical writer III position is available at Integrated Resources Inc. · Manage documentation and change order processes · Develop SOPs and associated technical documentation · Edit material prepared by SMEs or other personnel · ...

The job requires a technical writer to create and maintain technical documents. · Document control & review process of all technical documents. · Will work directly with Clients, and various departments to ensure documents are accurate. · ...

A Sr. Technical Writer is required with experience in writing detailed Functional Specifications and technical requirements to work in an R&D shop. · ...

The Deviation Investigation Technical Writing Consultant is an individual contributor role responsible for the authoring of deviations classified as Notice of Event, Minor, Major, and Critical deviations and associated investigations. · ...

+The Senior Technical Writer will be responsible for authoring,+ · reviewing and maintaining high-quality CMC and GMP documentation to support development,manufacturing testing and regulatory submissions for radiopharmaceutical products.+ · This role is heavily focused on analyti ...

The Technical Writer I is responsible for the development of controlled documentation in accordance with LifeCell policies and procedures. · Author changes to documentation. · Create new or revise existing content. · Participate in project team meetings. · ...

A client seeks a textual content specialist to improve customer-facing wording on mobile devices. · ...

The Client is seeking an experienced Web Content Creator/Copywriter to help create a best-in-class online identity for our corporate website. · This position creates, coordinates and repurposes multimedia brand content (text, photography and video) across a variety of corporate s ...

The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). This individual will be responsible for delivering CMC documentation to support the regulatory strategy for ...

This individual will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. · Co-authors/ authors scientific content for CTD ...

This individual will be responsible for delivering CMC documentation to support the regulatory strategy for the Cell Therapy clinical portfolio.The role requires effective collaboration across technical functions to deliver on timelines for submissions. · ...

This individual will be responsible for delivering CMC documentation (dossier and supporting documents) to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. · Co-authors/authors scientific content for CTD ...

The Technical Writer will sit within the Cell Therapy Development and Operations (CTDO) Portfolio Strategy and Operations (PSO) Pipeline Portfolio Management Office (PMO). The position interfaces with experts in Process Development, Analytical Development, Cell Therapy Technical ...

A technical writer is needed to assist with the authoring of documents for deploying Agile development in a Computer Systems Validated environment. · ...

This individual will be responsible for delivering CMC documentation (dossier and supporting documents)to support the regulatory strategy for the Cell Therapy clinical portfolio from early stage through registrational application. · Co-authors/authors scientific content for CTD Q ...

This individual will be responsible for delivering CMC documentation to support the regulatory strategy for the Cell Therapy clinical portfolio. · Co-authors/ authors scientific content for CTD Quality sections aligned with regulatory strategy. · Plan and facilitate submission ki ...

Our clients seek a Medical Technical Writer with pharmaceutical prescription drug related writing experience for an initial 6 month contracting role. · ...