Writer Salary at Frederator Studios BETA

Type of Requisition: Regular Clearance Level Must Currently Possess: Secret Clearance Level Must Be Able to Obtain: Top Secret/SCI Public Trust/Other Required: None Job Family: Technical Documentation Job Qualifications: Skills: Documentations, Quality Documentation, Technical Documents Certifications: None Experience: 5 + years of related experience US Citizenship Required: Yes Job Description: GDIT is looking for a Technical Writer for the USCENTCOM CITS Program in Tampa, FL. The appropriate candidate will produce professional technical and contractual documentation across the program. Duties and Responsibilities: - Develops, updates, and maintains technical documentation, user guides, and how-to materials to assist users across the CITS Enterprise - Creates staff packages and provides documentation including white papers, information papers, decision papers, point papers, PowerPoint presentations, spreadsheets, databases, SharePoint, training packages, policy, and guidance within Do

Working within the Global Marine and Navy business unit you will provide technical writing support to JCI and our customers. Client portfolio will cover UK and international navies but also commercial vessels such as cargo ships, tankers, ferries, and yachts. The role will involve developing technical documentation across several contracts. The documents will be contract specific and will be developed in accordance with the client’s specifications. The type of documents will be wide ranging including mechanical, electrical, and environmental. What we can offer Competitive salary 25 days holidays + Bank Holidays and sick pay Working hours Mon – Thurs 8.30am-4.55pm and Fri 8.30am-3.30pm Comprehensive benefits package including 7% match pension, free life assurance, employee assistance program, employee referral scheme, employee discounts including high street brands, cycle 2 work scheme and discount on Johnson Controls security products. Extensive product and on the job/cross training op

Type of Requisition: Regular Clearance Level Must Currently Possess: None Clearance Level Must Be Able to Obtain: Secret Public Trust/Other Required: None Job Family: SCA Job Qualifications: Skills: Documentations, Technical Manuals, Technical Writing Certifications: None Experience: 3 + years of related experience US Citizenship Required: Yes Job Description: Technical Writer III Job Description Technical writer to support Surface Ship Torpedo Defense (SSTD) systems technical data documentation requirements for US Navy and Foreign Military Sales (FMS) Provide technical writing support for the review and development of SSTD technical procedures, processes, and manuals that are published in MS Office applications, Adobe PDFs and IETM’s. Gather, process, analyze, reconcile and enter SSTD systems engineering data and fleet modernization data in support of Ship Alteration Systems, Temporary Alteration Records, Engineering Change Orders, Engineering Change Proposals, Navy Training System Pl

Masis Professional Group is assisting our client in searching for a Writer with proven experience in creating strategies and content for employee-related communications based out of Westborough MA. Position is a contract position to last at least 6 months with high potential to convert to a permanent role for the right candidate. Position is 100% onsite. Looking for experienced communications professional with strong writing and editing skills, creating engaging content, video scripts, and other projects to promote the company's brand internally. Salary is commensurate with experience ($75,000 and up) Schedule: Onsite, Monday through Friday, standard 40 hours Duties and Responsibilities: Write, edit, review, and oversee content for the company intranet and communications platform by partnering with other departments to ensure content is accurate, appropriate and timely. Analyze performance metrics and oversee the publication of news stories, while leading the Internal Communications (I

Our client, Biotechnology domain is seeking a OPERATIONS TECHNICAL WRITER to join their team. As a OPERATIONS TECHNICAL WRITER, you will be part of the client team OPERATIONS TECHNICAL WRITER 29851 Willow Creek Eugene Oregon 97402 United States 6+ Months Contract Shift timings Exact Schedule - 8am-430pm M-F Job Description How will you make an impact? The Technical Writer position is part of the Operations Project Management/Technical Documentation team in Eugene, OR. This position will support a manufacturing operation that produces products used for labeling and detection in cell biology, molecular biology, and related fields. What will you do? • Work in the Finished Goods Manufacturing Department to write work instructions for technical/scientific manufacturing operations. • Review and interpret historical production records and manufacturing documents to collect data and information about existing processes to make accurate changes to manufacturing batch records. • Work directly wi

Job Description Job Description Job Title: Deviation Writer/ Technical Writer Duration: 3+ months Contract Job Location: St. Louis, MO, 63134 Pay Rate: $43/hr per hour on W2 Responsibilities: • Analyze and investigate deviations or non-conformances, using problem-solving tools like root cause analysis. • Collect relevant data and information related to the deviation, and analyze it to identify patterns, trends, or potential causes. • Document findings in a comprehensive and objective manner, ensuring accurate recording of all relevant information. • Collaborate with various departments to gather information, evaluate causal factors, and implement corrective and preventive actions (CAPAs). • Provide timely written documentation of investigations and communicate recommendations based on investigation outcomes. • Participate in client communications and responses, working closely with program team leads, quality, and management. Education: • BS/BA in biology, biochemistry, chemistry, or o

The team is seeking a hardworking, results-focused Document Facilitator who will assist in the formatting, facilitation, and document approval process through GMP documentation systems. The position will work with analytical scientists in the delivery of complete and thorough analytical work packages to support clinical Biologic drug substances and drug products. This position will report directly to a Senior Manager within the Sample and Data Management (SDM) Group of the Analytical Strategy & Operations (ASO)-GxP Biologics department. Essential Duties and Responsibilities include, but are not limited to, the following: Edit and format GMP documents including Specifications, SOPs, and Technical Documents. Facilitate the routing of technical documents through required workflows. Review documents for grammatical errors and formatting. Work with several technical teams and collaborators at BMS Biologics manufacturing sites, including Analytical testing, Process Development, and Materials

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries. ABOUT ABBOTT Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology. This position works out of our Columbus, Ohio plant location in the Abbott Nutrition Division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to