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The Director, QC is a key member of the Quality Control Leadership Team responsible for the design, implementation, and continuous improvement of all processes/systems in support of the Quality Control testing program at the Bothell Cell Therapy manufacturing site.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Provide QA and CSV expertise within a manufacturing environment, specifically working with MES, DeltaV, and OSI PI systems. Manufacturing experience with a focus on MES, DeltaV, and/or OSI PI.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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This individual will be experienced working with Manufacturing Execution System preferably Syncade and perform application support duties for manufacturing execution system (MES) and will provide production support for label printing activities by collaborating with the Document Control team.
$57 an hourFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Prefer direct experience with common spacecraft subsystems such as Power Systems (Solar Arrays, Batteries), Secondary structures, Avionics assemblies, harnessing, ADCS elements and placement implications, Payload subsystems integration, Deployables, Release mechanisms, Moving mechanical assemblies, Thermal control systems and sizing (materials, finishes, MLI, HPAs, radiators), LV Interfaces.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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On-Board Scientific is hiring a QA Associate Specialist - Document Control in Bothell, WA! Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for BMS Jump site records management.
$50.99 an hourFull-timeExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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As the head of Biologics Development, you are responsible for the end-to-end, cell vial to product vial, development of biologics manufacturing processes, which include antibody, conjugation, formulation and drug product.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This is a key position that ensures the reliability of equipment for new Bio-Manufacturing Facility as well as maintaining the current operation of the existing facilities. Perform preventative maintenance work on complex manufacturing equipment such as bioreactors, processing pumps, valves, RO/DI water systems, distillation systems, distribution systems, steam generation, compressed air systems and other manufacturing and utility system equipment.
$49.55 an hourFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Strong knowledge of design control, change control, process validation and tech transfer, and in-vitro molecular diagnostic manufacturing. Work scope of this position includes management of key processes relating to quality engineering tasks, ensure robust design controls, supplier quality, risk management, tech transfer to manufacturing operations and driving KPI affecting quality in manufacturing.
$110,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Certain positions at Bruker require compliance with export control laws and as a result, all interviewed candidates for all positions will be screened pre-interview to determine their eligibility in light of export control restrictions.
$127,000 a yearFull-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The scope of this position includes quality engineering, support for design controls, supplier and incoming quality, risk management, and quality oversight over manufacturing processes. The Operations Quality Engineer II supports the quality system processes and activities associated with the manufacturing of NanoString products.
$127,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Job Title: QA Associate Specialist – Document Control. The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for Client Jump site records management.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The Laboratory Technician will use scientific knowledge and understanding to execute and document standard operating procedures to ensure successful manufacturing and on time delivery of Oligonucleotides.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Act as SME and lead the technical team at CMDO for late-phase adjuvant production (both lipopolysaccharide synthesis and oil-in-water adjuvant formulation), including tech transfer, scale-up, gap/risk analysis, process characterization/validation, cGMP manufacturing.
$200,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the Client Jump site, including the document change control process, issuance and reconciliation of batch records, batch related forms, product labels, and management of archival and retention of GMP records.
$51 an hourExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for BMS Jump site records management. Quality - QA Associate Specialist – Document Control.
ExpandApply NowActive JobUpdated 4 months ago
manufacturing document control jobs in Bothell, Peoria, Arizona
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