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Boeing has an exciting opportunity for an Entry-Level and Associate Quality Specialist to join our dynamic team in multiple locations across the United States. These positions must meet Export Control compliance requirements, therefore a “US Person” as defined by 22 C.F.R. § 120.15 is required.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The position will also assist in other quality and compliance activities, including, but not limited to, deviations, CAPAs, change control, supplier quality, audit management, and inspection readiness.
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4 - 6 Years Experience within Document Control (processing, verification, and archiving); Quality Assurance, Quality Systems, or related role in a GxP-regulated biopharma, medical device, or similar industry.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Ensures top-quality standards by performing detailed inspections using advanced equipment, including CMM and Zeiss CT Scanner (training provided). Assist with Measurement System Analysis (MSA) and Statistical Process Control (SPC) studies.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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To better serve the global auto industry electric vehicle trend in the United States, CATL, through its U.S.-based subsidiary, CATK, is seeking multiple dedicated and detail-oriented Incoming Quality Control (IQC) Specialists to join our quality assurance team.
ExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The company has implemented an QMS software- MasterControl to manage and integrate their quality related functions for Training, Document Control, SOP Management, CAPA, Deviation, Change Control, Audit management, integrated business process management.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Knowledge of Six Sigma, Define-Measure-Analyze-Improve-Control (DMAIC) methodology, performance measures and quality improvement statistics preferred. Act as a project engineer/manager for medical device QMS quality improvement activities, with a focus on design controls and risk management.
ExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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The Quality and Regulatory Documentation Specialist will contribute as a member of the Quality team at TheBioBox, LLC/ Restem, LLC. The Documentation Specialist will support all aspects of quality and regulatory documentation, quality system implementation, document management, and change control to ensure that the documentation system, procedures, and records meet quality standards and regulatory requirements.
ExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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Performs all Document Control functions to assure compliance with the company quality system and contributes to the management of the electronic QMS system. Contributes to establishing document approval and change control procedures in addition to assisting other department personnel in formatting all quality system documents.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Collect metrics to assist with monitoring Quality Systems (deviations, CAPA and change control, external and internal audits). This position will be primarily responsible for GMP product support, and administering quality systems such as supplier qualification, deviations, CAPAs, and change control.
ExpandApply NowActive JobUpdated 26 days ago - UpvoteDownvoteShare Job
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These positions must meet Export Control compliance requirements, therefore a “US Person” as defined by 22 C.F.R. Quality Salaried professionals’ partner with and lead cross-functional business units to protect the integrity of products and processes, effectively ensuring that every product and service meets quality and regulatory requirements.
$97,750 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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One of our large Pharmaceutical clients is seeking a Quality Engineer Specialist to oversee and support an external manufacturer within Advanced Therapeutics in Rockville, Maryland. In this role, you will be providing quality oversight and validation support for manufacturing activities related to commercial operations for production of cell therapy products.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Our well estblished pharmaceutical client is looking for a Senior Quality Specialist to join their growing team. Support/Maintain site Document Control System. Bachelor’s degree in relevant scientific quality assurance / technical field.
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Central Transport, LLC, one of the nations most trusted and technologically advanced transportation firm, is currently seeking a Quality Assurance Specialist (HU Control Supervisor) for our facility located out of Detroit, Michigan.
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Responsible for the development, implementation, and maintenance of incoming material standard procedures for the factory from sampling to disposition including but not limited to routine, investigative and monitoring programs in collaboration with R D, procurement, and Quality Control.
ExpandApply NowActive JobUpdated 16 days ago
quality control jobs Title: specialist quality in New Orleans, Hauula, Hawaii
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