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Provide well-researched written content through a variety of mediums, translating technical content into well-understood information utilizing our organizational tone of voice and writing style.
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Strong documentation, technical writing, and communication skills. Must have at least 3 years of biotech/pharma process engineering experience. A leading pharmaceutical company in North Carolina is in immediate need of 2 Process Engineers to join their team for a 6-month project.
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Support deployment projects across the Fidelity EnterpriseDevelop program deployment schedules in conjunction with the requesting business units and all supporting technical groupsDevelop scorecards and reporting for program status to senior management and business unitsAbility to effectively deal with rapid change in a positive manner and to lead through changing priorities.
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The Technical Writer, reporting to the Director of Facilities will be responsible for writing and developing Standard Operating Procedures (SOPs) and other process documents for the Facilities and Engineering (FandE) department.
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Working knowledge of programming languages (e.g., Python, Matlab, LabVIEW) and experience with data analysis, signal processing, statistics, and technical writing. The successful candidate will be responsible for planning and executing key project deliverables, which includes generating creative design solutions to complex technical problems.
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Experience with creating and writing technical documents using MS Office products, Visio, Word, Excel, PowerPoint and JIRA. *Required 6 Years. Technical hands on knowledge in specialized areas of web application system analysis and programming: Java, J2EE, with JavaScript, XML and XSL *Required 7 Years.
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The Technical Director will work closely with the technical leads, SI Director, Program Management Director, and Country Directors to cascade the technical approach and ensure country work plans are in alignment.
$90,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Drive technical research to understand customer and clinical needs, develop insights and recommendations through scientific literature review, technology landscaping, and ethnographic research.
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Technical writing and document review experience (i.e. deviations, change requests, standard operating procedures, batch records, protocols, etc.) Provide technical/cGMP expertise in non-routine situations, guide decision making based on SOPs, process CPPs, CQAs, process validation, etc.
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Must be able to effectively communicate verbally and through technical writing (documentation of laboratory experiments). Under general guidance, prepare technical reports and/or CoAs to summarize data and document experimental conclusions.
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In-depth knowledge in one or more analytical topic areas: HPLC, GC, KF moisture testing, MDI/DPI performance testing. University degree (BS or MS) in the field of chemistry, pharmaceutical science, or related field.
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In this Small Scale Manufacturing (SSM) Manufacturing Specialist II role, you will be responsible for manufacturing support tasks including technical writing, project management, and process implementation.
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7+ years of experience in technical writing. Hands-on experience with business or financial writing; creative copywriting, including experience in an agency or in-house creative department.
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Experience in the use of software tools for data entry and analysis such as (LIMS); Well-developed technical writing skills. Experience in the use of software tools for data entry and analysis such as (LIMS); Well-developed technical writing skills.
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Keep abreast of current medical and/or technical writing/regulatory knowledge, including Good Clinical Practice (GCP), along with developments and advances in drug development/medical and/or technical writing.
$124,400 - $211,900 a yearFull-timeExpandApply NowActive JobUpdated Today
technical writing jobs in Durham, NC
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