Technical Writer - Parsippany-Troy Hills, NJ

We recruit top-notch talent for over 40 Fortune and Government clients coast-to-coast across the U.S. We are one of the fastest-growing companies in the U.S. · ...

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

Dice is the leading career destination for tech experts at every stage of their careers. · ...

· Elevate your career at Marotta Controls, a New Jersey Top Workplace three years running  Dedicated to innovation, quality and excellence, we deliver cutting edge control systems for the Aerospace & Defense industry. At Marotta, we value bold thinking and teamwork, and we empow ...

This is a Technical writer position to support the set up and change management of stability studies. · Supports internal customers in the set up and change management of stability studies. · Prepares submission-ready reports on stability data. · ...

Previous experience with SDLC and GLPGCP validation is preferred Technical writing or documentation experience in a regulated industry is preferred. · Bachelors Degree in Computer Science or related field · ...

Technical writer with experience in regulated industries. · ...

Supports internal customers in the set up and change management of stability studies fielding stability related queries concerning marketed pharmaceutical products and active pharmaceutical ingredients prepares submission ready reports on stability data. · May be involved on limi ...

We are seeking a technical writer to assist with CSV validation in a regulated industry. · Previous experience with SDLC and GLPGCP validation is preferred · Technical writing or documentation experience in a regulated industry is preferred · ...

We are seeking a Technical Writer to develop, manage, and maintain accurate, compliant technical documentation for aerospace systems and programs. · ...

Write documents for drug metabolism and bioanalysis within Client Nonclinical Disposition and Bioanalysis (NDB). Review data to determine the appropriate tabular and textual formats. Work with scientists in NDB to ensure proper presentation of data. · ...

We are one of the fastest growing IT Consulting company across the USA and we are hiring "Validation Technical Writer" for one of our clients. We offer a wide gamut of consulting solutions customized to our 450+ clients ranging from Fortune 500/1000 to Start-ups across various ve ...

The team support all of Summit West. The technical writer will work with teams to understand documentation requirements and system operations. · Ability to provide efficient, timely, reliable, and courteous service to customers. · Ability to effectively present information. · ...

Prepare technical documents and maintain existing ones. Review and revise content for accuracy and quality. · ...

· Company Description · About BCforward · BCforward began as an IT business solutions and staffing firm. Founded in 1998, BCforward has grown with our customers' needs into a full service personnel solutions organization. BCforward's headquarters are in Indianapolis, Indiana and ...

+These positions are to work with the Toxicology group at Bristol Myers-Squibb as a Nonclinical Safety Writer. · + · +Partner with Toxicologists on drug development programs to support regulatory document preparation and review. · Provide document and word processing support in t ...

We seek a Scientific Writer with strong scientific background and experience in writing manuscripts for publication in peer-reviewed journals to join a cross-functional publication team. · The successful candidate will develop, manage and execute publication plans of one or more ...

+Job summary · We believe in providing staffing solutions to address the current talent gap - Right Talent - Right Time - Right Place - Right Price and acting as a Career Coach to our consultants. · +QualificationsBachelor's degree in a related field from an accredited college or ...

The Tech writer for CAR T Systems and services works independently and is responsible for authorizing high-quality documentation in support of GMP manufacturing. · Author and revise documents as needed. · Manage the development of documents through the document management system ...

This position designs and develops training materials, edits, and maintains all training content for all U.S. REMS functional roles. · ...