- Aequor (Seattle, WA)
- …in group meetings and contribute to group discussions and team strategy. Author technical reports, protocols, and study memos.Basic Qualifications: STEM degree ... teams Ability to communicate clearly and concisely through oral presentation and technical writing Ability to leverage literature, internal and external resources to… more
- Aequor (Thousand Oaks, CA)
- …sites and business partners 3) Manage complaint return sample inventory 4) Author technical assessment reports Requirements: Bachelor's Degree in Life Sciences ... or related field or the equivalent combination of education and/or experience. Typically 2 plus years of related quality assurance or manufacturing experience in a GMP pharmaceutical or medical device industry. Evaluate documentation and operation according to… more
- Newbold Advisors (Herndon, VA)
- …to Federal Government solicitations Lead and write responses for technical , management, corporate experience, staffing, and transition sections. Collaborate with ... SMEs to develop compliant, compelling solutions. Gather and synthesize information from various stakeholders to support writing activities. Write clear, persuasive, and compliant proposal sections for complex bids. Experience in a competitive proposal… more
- Rose International (Hoffman Estates, IL)
- …electro-mechanical equipment Knowledge of Extended Reality creation sw suitesResponsibilities: Create and Author Technical Service Content intended for use by ... to create extended reality (augmented reality) service experiences Understanding of Technical Content creation (Written, & Multimedia, XR) Ability to create… more
- Axelon Services Corporation (Seattle, WA)
- …and documentation - Summarize and present data in group meetings and contribute to group discussions - Author technical reports, study memos, and protocols ... Associate Scientist or Scientist, RNA Process Development Location: Seattle, WA * 100% Onsite Top Skills: - Proficiency with biochemical techniques to analyze oligonucleotides (PAGE and CE) - Proficiency with analytical IP-RP chromatography for RNA (including… more
- Careers Integrated Resources Inc (Oceanside, CA)
- …of biologics drug product processes o In-use stability and administration * Author protocols, technical summary reports/memos and tech transfer documentation ... thinking, as well as be familiar with the relevant technical literature. Knowledge, Experience and Skills: * Degree in...to company goals. * Excellent communication (both verbal and technical ) and interpersonal skills are required. * Demonstrates … more
- Insmed Incorporated (San Diego, CA)
- …of situations or data requires an in-depth evaluation of variable factors; Author Standard Operating Procedures, technical reports, process descriptions, ... is the role for you. This is a non-supervisory position.ResponsibilitiesExecute technical strategies for purification process development to support pre-clinical and… more
- Raytheon (Tucson, AZ)
- …a safer, more secure world. As the Modeling & Simulation Engineering Technical Fellow, you will participate in unique multi-disciplinary research across integrated ... is heading or needs to go, while considering the technical aspects of how to get us there and...to internal stakeholders and external customers Must be the author of intellectual property (patent disclosures) and conference/journal publications… more
- American Honda Motor Co Inc (Greensboro, NC)
- …primary structure. Duties and Responsibilities: * Serve as subject matter technical expert stress engineer responsible for development and verification of structural ... * Provide support to team members for creation of analysis tool automation. * Author test plans and reports for component testing including test article, test setup… more
- Axelon Services Corporation (Seattle, WA)
- …setting, that includes non-clinical, clinical, regulatory, and CMC functions - Author , review, and approve technical documents, including methods, protocols, ... Top Skills: - Expertise in cellular and/or molecular immunology is required. Prior research with cell therapy products (ie autologous or allogeneic T/CAR T cells, HSC and/or iPSC) will be prioritized - Experience with analytical platforms for the… more
- Aequor (Bothell, WA)
- …an individual contributor. The CSV Contractor will partner with Business Owners, Technical Owners, and Quality to create and manage validation deliverables for ... and Quality in accordance with company procedures and regulatory requirements. Author , review and/or approve applicable CSV documentation Assist Business Owners and… more
- Merck & Co. (Durham, NC)
- …of investigations.Review of various records impacting batch release.Serve as a technical subject matter expert (SME) in selected quality systemsProvides support to ... other departments to ensure appropriate root cause and CAPAs are determined . Author /revise SOPs, methods, protocols, and trend reports .-Provide support to all… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Biotech is seeking Director, Global Process Validation as part of the Technical Operations team based in Raritan, NJ.Role OverviewThis position represents a critical ... validation program by adhering to industry best practices and sound cell therapy technical principles to ensure that the commercial process is maintained in a… more
- Aequor (Seattle, WA)
- …Laboratory Notebook (ELN) entries thoroughly and on timely basis, and author development reports when relevant Work with cross-functional stakeholders and partners ... to support quick turnaround-times Participates in troubleshooting of routine technical or operational problems and initiative related to continuous improvement… more
- Aequor (Providence, RI)
- …handles product quality and stability data and may serve as a primary author on regulatory filings and directly participate in and support site-based GMP ... new roads for helping patients. Key Responsibilities include: Build and maintain technical GMP documents and product stability studies Review, verify, report, and… more
- Merck & Co. (Lower Gwynedd, PA)
- …to junior staff, build relationships with stakeholders, and provide expert technical representation on multidisciplinary teams. The candidate should be current on ... to lead group in complex multiparameter data analysis, interpretation and summary. Author regulatory filings and respond to regulatory authority questions pertaining… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to ensure the compliance for products marketed and/or distributed locally. May author or review stability studies protocol or reports. Provide the support for ... management and update of technical registration documents- Quality Metrics: Collecting and analyzing data related to deviations, CAPA, Change Controls, OOS, and… more
- Merck & Co. (Durham, NC)
- …inventories, and transports all required equipment, materials, supplies and products. Author , review, and/or edit procedures and technical documents to ... support regulatory filings including standard operating procedures, job aides, and learning documents. Performs general maintenance and assists or ability in troubleshooting of equipment independently. Performs housekeeping in all work areas. Executes facility… more
- Merck & Co. (Durham, NC)
- …process improvement or learning events, as guided or approved by Quality management Author , review, and approve SOPs Participate in Kaizen events Direct support of ... requests from clients and/or customers Problem Solving Supports resolution of technical and operational problems through collaboration with peers Consults on an… more
- Aequor (Newbury Park, CA)
- …Sciences Digital and Pivotal Portfolio (ASDP) group provides scientific and technical engineering expertise in support of 's pipeline and commercial portfolio. ... to gather template requirements. Once requirements are gathered the role will author , revise, and deploy assay templates. Additional responsibility of the role will… more
