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Use of Laboratory computer systems and GMP Quality Systems such as: TrackWise, LIMS, DMS, LMS. Demonstrated experience, leadership, and independence with QC functions associated with the GMP production and testing of cell/gene therapy products or biologics in both clinical and/or commercial settings.
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The Janitorial & Clean Room Technician is responsible for performing all routine and specialized cleaning and sanitizing of our biopharmaceutical manufacturing areas in compliance with Good Manufacturing Practices ("GMP") and in accordance with Standard Operating Procedures ("SOP.
$41,600 - $52,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Micro-Cleaner is a critical role in the company which ensures the proper cleaning of the cleanroom, controlled environment and GMP laboratory environments. Responsible for participating in continuous training: cGMP training, technical skills, safety, performance improvement.
$19 - $20 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Write and revise standard operating procedures (SOPs) for GMP Analytical and Microbiology laboratory operation and instruments. Minimum of 5-8 years’ experience in a GMP laboratory environment.
$52 - $62.29 an hourExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Lean Six Sigma Green Belt certification is a plusExperience with Agile configuration product management software - preferredExperience with Oracle and DataSweep or other electronic device history record system - preferredExperience working in a manufacturing and/or laboratory environmentGood written and verbal communication skillsSkills/Abilities:Ability to work independently as well as within a team of professionals.
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Performs routine and non-routine testing with expert proficiency and general QC laboratory work for release of Direct Raw Materials to support Seagens clinical development and/or commercial products in a GMP testing environment.
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In this role, you will have the opportunity to:Synthesize small organic molecules and perform routine analysis using HPLC, LCMS, FTIR, UV, NMR and other analytic instruments under a GMP environment.
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Performs, or oversees internal or external testing laboratory performance of routine and non-routine testing and general QC laboratory work for the facility and utility system monitoring, in-process support, release clinical development and/or commercial products in a GMP testing environment.
Full-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Experience with Veeva EDMS preferred, or similar. Excellent technical writing skills, close attention to detail and excellent follow up. Knowledge of electronic document management systems (EDMS) to complete workflow of document to final approval by uploading the word document into EDMS.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Performs routine and non-routine testing with expert proficiency and general QC laboratory work for release of Direct Raw Materials to support clinical development and/or commercial products in a GMP testing environment.
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This position is responsible for the harmonization, life-cycle management and continuous improvement of all GMP quality system elements within the Laboratory Systems technology platform including but not limited to LabWare.
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4+ years of experience working in a GMP laboratory. Applying the principles of good manufacturing practices (GMP) on a daily basis. Participation in Laboratory or Out of Specification Investigations.
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Responsibilities will include in-process and drug substance sample testing, training of laboratory staff, GMP document authoring / revision, providing oversight in support of GMP operations and spearheading initiatives to build infrastructure and processes across both Washington state facilities.
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Perform data verification, data review and review of GMP documentation for multiple systems (general and complex) and/or products. Family care services such as adoption and surrogacy reimbursement, fertility/infertility benefits, support for traveling mothers, and child, elder and pet care resources.
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Job Title: Technical Writer. Schedule cross functional team meetings, collect feedback, create draft documents, post on sharepoint, schedule reviews, collect and resolve feedback. A self-starter with an ability to manage electronic systems with minimal training and supervision.
$55 - $63 an hourExpandApply NowActive JobUpdated 12 days ago
gmp laboratory jobs in Bothell, WA
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