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Under the supervision of a Regulatory Specialist and/or Department Management, provide support in writing submissions, design dossiers, technical files as required by global medical device regulations to obtain product clearances and or approvals for commercial distribution within targeted selling market.
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GMP Pharmaceutical/Vaccine laboratory work including technical writing including protocols/reports. Technical writing experience preferred in a GMP/GLP environment. Serve as the technical lead for qualifications and ensure methods are aligned with equipment functions.
$35 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Preferred Experience and Skills: Supply Chain- contacting vendors, Procurement skills (analyzing/forecasting), Facility/Warehouse inventory management, Experience working in an operations support role, Technical writing – including investigations, SOPs.
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Required top skillsets- Investigational Technical Writing Skills and Deviation management authorizing experience. 1) Investigational Technical Writing Skills. Post-Bachelors degree experience in a cGMP environment (e.g. Production, Development, Process Engineering, Technical Services, or related field) in the pharmaceutical/ biotech industry.
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Technical skills to be able to navigate. Materials Management (MM) supports R&D activities in the manufacture of clinical, stability, and developmental supplies by procuring and dispensing materials to internal Pilot Plants and external Contract Manufacturing Organizations.
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Minimum 2 years of technical writing and instruction design experience from a curriculum/training content creation perspective. Our large pharma client in West Point PA is looking for a Learning Professional to join their team to design, develop and support learning and development activities associated with the manufacture, testing and release of products in support of the site's learning strategy and integrated learning plan.
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Must exhibit comfortable interaction with technical staff including laboratory managers, Medical leaders, and other technical personnel. Handles all payer, physician and patient contact received by telephone and in writing.
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Our unique boot camp program for new technical hires is comprised of sessions designed to provide context around clinical trials, what we do within our platform and how, and a taste of what our developers are asked to build in real clinical trial studies.
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Assist with the coordination of the technical review process among internal specialists including civil and electrical engineering, energy assessment, technology, and permitting teams, and synthesizing and writing due diligence reports.
$80,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Along with detailed documentation focus and sound technical writing skillsWorking knowledge of MS Office (Word, Excel, a must. Duties and Responsibilities Provide professional and technical support to multiple Westwood projectsDue diligence and site investigationSite design including facility plan & profile, cross sections, grading and erosion control plans, and stormwater management facilities.
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Strong proficiency in Microsoft Office Suite and technical writing. Join KEMA Labs, a division of CESI a global leader in technical consulting and engineering for the electrical power sector.
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