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At least one year in quality assurance role in medical device industry is preferred. Conduct spot-check inspections/audits of production operations• Participate in the internal audit program• Write, review and approve Standard Operating Procedures (SOPs) as necessary• May assist in supporting the Document Control program, record retention areas, and sample retention areas• May support returned instrument processingo Log returned instruments from the field.
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2+ years’ of laboratory and/or quality control experience. Provide support for technical and quality issues as needed. Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production.
$27 an hourFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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In this role you will provide support for product quality assurance, process improvements and all quality system program at the Westbrook Site. Working knowledge of FDA, cGMPs/QSR and ISO quality system requirements Strong technical writing skills and effective communication skills An equal opportunity employer, Client welcomes and encourages diversity in our workforce.
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Ability to follow Good Manufacturing/Laboratory Practices GMP and GLP. Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
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Responsible for developing, monitoring, and making recommendations to improve overall departmental quality. Ability to gather quality reports with understanding of the quality indicators being monitored.
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Participate as a team member to develop strategies to improve product quality. Certified Quality Auditor (CQA) or equivalent. If you are a person with a relentless drive to succeed, a strong focus on quality with a passion for success – join us today.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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We are promoting this job opportunity as provided by a third party, the employer.
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Founded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances.
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Perform a wide variety of activities to support the Quality Management System. Title: Quality Control Technician. May assist in supporting the Document Control program, record retention areas, and sample retention areas.
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Working knowledge of FDA, cGMPs/QSR and ISO quality system requirements. Demonstrates commitment to the development, implementation and effectiveness of Quality Management System per ISO, FDA, and other regulatory agencies.
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Develop, implement, and maintain quality assurance processes and procedures. Proven experience in quality engineering within a manufacturing environment. Certification in Quality Management (e.g., CQE, Six Sigma) is a plus.
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The Pharmacy Quality Improvement Specialist is responsible for generating process improvements that bring about measurable improvement in quality and/or efficiency. Working Specialty or Front-end Pharmacy operations preferred.
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Experience with quality documentation such as non-conformance and risk assessments, CAPA, and related documentation. In this role, you will directly participate in a Quality Systems Remediation Program, focusing on the creation of high-quality written content.
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They need to be able to understand quality systems, work with teams who have documentation routing through the system and be able to summarize the activities. We need someone with a lot of familiarity of the quality management system (Agile.
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The position of Senior Supplier Quality Engineer is within our Infectious Disease Developed Markets Business located in Scarborough, ME. The Senior Supplier Quality Engineer will be responsible for activities related to supplier selection and evaluation, material qualification, supplier performance and receiving inspection.
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Title: quality assurance inspector Company: Technology Publishing Co in Portland, ME
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