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Minimum 5 years of experience in a biotech or pharma with relevant work experience within a quality control team. Lead CAPA projects (or work closely with Quality Assurance) related to product quality or non-conformities and investigate customer complaints.
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Responsibilities include but are not restricted to the following: collaborate with R & D for new product transfer and consult to resolve issues with QC test strategies; collaborate with manufacturing, process engineering and QA for non-conforming product troubleshooting and resolution; develop strategy, organization, including process improvement to ensure the Quality Control meets business expectations.
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Final Quality Control Inspector (LHRR) Verify that production activities documented in LHRs are consistent with approved manufacturing processes, work instructions, and quality control plans.
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PREFERRED CANDIDATES SPEAKS SPANISH. Skills:Materials Management, Wood manufacturing , Tape Measuring , Blueprint Reading, Microsoft Office, Spanish, Quality Control, MS Office, Blueprints, Quality Assurance, Manufacturing Experience:Entry Level1 year(s) responsibilities: Keeps track of the goods and supplies in a store or warehouse and manages orders to facilitate sales or production.
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The Quality Control Associate - Sequencing Cartridge Operations will be an integral part of a team that performs cartridge assembly and systems testing. This individual will be responsible for the setup, execution, monitoring and data analysis of all Quality Control release activities associated with the Sequencing Process.
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Minimum of 3-5 years of experience in SMT Quality Assurance Control/Inspection process per IPC-610 class 2,3 (PCBA and Mechanical components) Performs product inspection and/or audits of quality control programs.
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10+ years quality control (QC) or product engineering experience in PCB, semiconductor or similar process manufacturing fields. Process Quality Control Director - (88418) Recognized as a technology leader, Sanmina Corporation provides end-to-end manufacturing solutions, delivering superior quality and support to Original Equipment Manufacturers (OEMs) primarily in the communications networks, defense and aerospace, industrial and semiconductor systems, medical, multimedia, computing and storage, automotive and clean technology sectors.
$139,000 - $175,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Performs setup, execution and monitoring of Sequencing process for the Quality Control release of cartridge assemblies. Conduct data analysis of test results and determine Quality acceptability per approved procedures.
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The position requires an individual who works independently and in a team environment, experienced in cGMP requirements, quality control, attention to detail, and excellent communication with other functional areas and sites.
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Our client, a global leader in life sciences and diagnostics, is looking for Quality Control Associate in Santa Clara, CA. Review, generation and sign-off quality documentation. Maintain records and QC lab environment to comply with cGMP, OP(Operating Procedure) and regulatory requirements.
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Perform safety and occupational health management, surveillance, inspections, and safety enforcement for the Contractor.
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Inspect in-process or finished production assemblies and sub-assemblies for conformance to quality assurance standards. Performs a variety of inspection procedures to ensure quality levels at various stages of manufacturing at or above the standard.
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The individual will be responsible for review, generation and sign-off of quality documentation. Experience working in GLP, cGMP or ISO regulated environment X. Maintain records and QC lab environment to comply with cGMP, OP and regulatory requirements.
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Provide direction to access control team members, utilizing proper judgment to solve problems and to escalate matters as needed; Provide direction and guidance with new and existing policies and procedures, as necessary; Supervisor is responsible for quality assurance of all application and drafting support mappers required daily tasks.
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Three to six years of experience in Custodial Quality Control procedures and demonstrate ability to utilize existing programs as well as ability to create and administer new programs. Bachelor's Degree or two years of Quality Control experience in addition to requirements below.
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quality control jobs Title: control in Cupertino, CA
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