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As a senior specialist in Ad Tech, your role within our AdTech team will necessitate a strong grasp of current digital advertising ecosystems, product development cycles, and advertising technology stacks.
$90,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The primary focus of the Sr QA Specialist role will be to support biologics programs to ensure consistent compliance with regulatory and industry expectations. Omeros is seeking a highly motivated individual to join the Quality Assurance team as a Sr QA Specialist to play a key role in supporting cGMP quality operations.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Immediate need for a talented QA Associate Specialist – Document Control. Some technical writing skill set and be able to critically review documents while effectively inputting and expressing Quality principles Position Reports to Jenna Walker – Associate Director, QA Training & Document Control Education: Bachelor’s degree or equivalent Key Requirements and Technology Experience: Minimum of 1 year of relevant document control experience in a cGMP/FDA regulated environment.
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Job Title: Quality - QA Associate Specialist. The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
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As an Ad Tech Specialist your role within our AdTech team will require strong knowledge of current digital advertising ecosystems, product development cycles, and advertising technology stack. Troubleshoot and QA ad related products, technology, and performance within digital platforms (desktop, mobile, APP, CTV/OTT.
$60,000Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Associate Director, QA Training & Document Control. Managing an electronic document system for the Cell Therapy Above-Site which includes reviewing and approving document change requests, troubleshooting and releasing documents to an effective state.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Strong computer skills with MS Office (e.g. Word, Adobe, Visio and Excel) and with Quality Systems (e.g. Document Management System, Quality Management System) Assist with cross-training of Document Control personnel and customers to ensure adherence with procedures.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Sr. Quality Assurance Specialist - QA Operations. The Sr. Quality Assurance Specialist will work a Hybrid schedule and will need to be local to the Seattle, WA area. The wage scale for the Sr. Quality Assurance Specialist position is $95,000 to $120,000 per year.
$95,000 - $120,000 a yearFull-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Testing and providing final QA/QC of project deliverables before a client is ready to go live. As our Customer Success Manager (Deployment), you will work on industry-changing projects, building the digital network model that is deployed to our customers, and work closely with sales, customer success, product and engineering to ensure customers are provided an exceptional onboarding experience.
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On-Board Scientific is hiring a Quality - QA Associate Specialist of Seattle, WA! The Associate Specialist is responsible for activities in accordance with corporate policies, standards, procedures, and Global cGMP in support of the QA Disposition group.
$37.36Full-timeExpandUpdated 4 days ago - UpvoteDownvoteShare Job
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JOB DESCRIPTION: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Cell Therapy Above-site organization, including the document approvals, document change control process, periodic review and system reporting.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Minimum two (2) years academic, biotechnological, or pharmaceutical industry hands on QA experience in a GMP biologics manufacturing environment. They have pioneered groundbreaking cystic fibrosis treatments and cutting-edge cancer therapies that help a child's immune system defeat cancer, and made other major contributions to pediatric medicine.
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Job Description: The QA Oversight Specialist provides support to all functions associated with manufacturing and quality control operations via daily on-the-floor support. QA oversight of aseptic processing.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Project Control Specialist/Office Engineer/Document Control Specialist. QA Inspectors Concrete, Asphalt, Structural, MEP etc. Project Control Specialist/Office Engineer/Document Control Specialist.
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Foster cross-departmental relationships (QC, Materials Management, IT, Manufacturing, QA, and site leadership) by representing Validation at team meetings. Expertise in MES/Delta-V/LIMS/Lab Equipment and Manufacturing CSV systems.
ExpandApply NowActive JobUpdated 7 days ago
qa specialist jobs in Seattle, WA
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