- The Boeing Company (Mesa, AZ)
- …Commercial Airplanes** (BCA) is looking for an **Associate, Experienced, or** **Senior Writer Editor - Technical Communicator** to join our team in **Mesa, Arizona** ... nomenclature and navigation systems for multifaceted projects. Resolves issues regarding regulatory and legal requirements. Defines new standards and guidelines. +… more
- Insight Global (Raritan, NJ)
- Job Description We are seeking a detail-oriented and experienced Technical Writer to support the documentation needs for one of our largest pharmaceutical clients ... (operators, engineers, QA personnel). Ensure all documentation aligns with regulatory standards (GMP, FDA, etc.) and internal quality requirements. Maintain… more
- Kuehne+Nagel (Plymouth, MI)
- …also so much more than we imagine. **** You as Customs Entry Writer will communicate with customers, freight forwarders, and other departments to obtain necessary ... countries, major cities and ocean ports along with basic knowledge of US Regulatory Laws + Basic knowledge of INCO terms, the Harmonized Tariff Schedule, Customs… more
- Bank OZK (Little Rock, AR)
- …& Abilities + Knowledge of banking or finance within the scope of a technical writer . + Ability to communicate effectively both verbally and in writing, with a keen ... and tasks simultaneously, with exacting deadlines. + Ability to follow regulatory and Bank policy, procedures, and guidelines, including rules and regulations… more
- Guardian Life (Bethlehem, PA)
- …of our Group Underwriting organization. As the Group Underwriting Senior Technical Writer in Group Benefits Underwriting, you will collaborate with colleagues in ... IT to gather source material and validate content. + Familiarity with regulatory standards and documentation practices in insurance. **You have:** + Proficiency in… more
- CH Robinson (Atlanta, GA)
- CH Robinson is seeking a Senior Customs Entry Writer for our office in Atlanta. In this role, you'll be recognized as role model for account management excellence ... and seizing opportunities to demonstrate their professionalism--thorough knowledge of regulatory requirements and supply chains, and ability to create meaningful… more
- AbbVie (North Chicago, IL)
- …Job Description Key Responsibilities + Serve as a lead on complex clinical & regulatory documents. + Work closely with the team(s) on document authoring & content ... control of other functions involved in the production of clinical & regulatory projects. + Communicate deliverables needed, writing process, & timelines to team… more
- AbbVie (Chicago, IL)
- …. Job Description Responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company ... objectives. Responsibilities: *Independently prepares most clinical and regulatory documents needed for the development of AbbVIe drugs and/or devices. *Coordinates… more
- AbbVie (Chicago, IL)
- …. Job Description Responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company ... objectives. Responsibilities: * Responsible for leading and writing clinical and regulatory documents for drug and/or device development in support of company… more
- AbbVie (Chicago, IL)
- …. Job Description Purpose Responsible for leading and writing clinical and regulatory device and drug documents in support of company objectives for the ... (eg briefing books, IND, protocol, CSR, NDA sections, and regulatory response as well as CER, IDE and PMA)....other functions involved in the production of clinical and regulatory documents. Arranges and conducts review meetings with the… more