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The QC Supervisor will oversee inspections and testing of materials, quality, and endurance. Quality Control, Supervisor We are looking for a Quality Control Supervisor to join our Wilmington, MA team.
$85,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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It will combine the responsibilities of a Program Supplier Quality Manager and Fielded Supplier Quality Engineer with a primary focus on process and product improvement for materials that will be shipped or drop shipped as RTX furnished material to our customer's Certified Round Assembly Facility (CRAF) in Germany.
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Fusion Optix is seeking a highly skilled and detail-oriented Quality Technician to join our Assembly Group responsible for manufacturing specification grade LED lighting products. Proven experience as a Quality Technician or similar role in a manufacturing environment, preferably in the production of LED lighting products or electronics.
$32 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Johnson & Johnson Abiomed is recruiting for a Staff Quality Systems Specialist. Experience in Quality Systems, Quality Engineering, Quality Assurance, or other technical work experience.
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Experience with the use of quality systems and tools (for example, CAPA, Six Sigma methodology, change control, Statistical Analysis, Control Plans, and document management) Coordinate and serve as technical representative with management, manufacturing engineering, regulatory, and product management on all issues related to quality assurance and compliance.
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A strong technical background and proven track record in Quality Control with methods related to cell biology, biochemistry, and molecular biology. The scope will also include generating certificates of analysis/testing (CoA/CoTs), standard operating procedures (SOPs), and oversight of CTLs. The individual will also assist in managing quality events (OOS, OOT, Deviation, Change Control, etc.
$140,000 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Minimum of 5+ years of progressive Quality experience working in regulated environment preferably in the field of biotechnology, biopharma, and/or cell/gene therapy (deep experience with GLP or GCP preferred.
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Adaptable to perform in a fast-paced environment while still delivering high-quality results, this Analyst I - QC Molecular Biology will be required to have strong interpersonal skills and be able to work under minimal supervision.
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Author and review SOP changes; participate in change controls, CAPAs and other quality systems. Work independently and as a team player with quality and attention to detail. Promote and actively demonstrate the Lantheus values of Accountability, Quality, Efficiency, Customer Service, Collaboration, and Safety, as well as appropriate workplace behaviors and professionalism, including respect, flexibility, and a positive attitude toward work and others.
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Minimum 2 years' experience in Quality Engineering, Quality Assurance, Manufacturing Engineering, or Design Engineering. The Quality Engineer (electronics and lighting) will develop and enhance products and manufacturing processes, oversee quality standards, and implement quality control systems.
$90,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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American Society for Quality (ASQ) credentials. MedTech Quality Systems organization leverages modern technology solutions, data, real-world insights, and creative minds to support development of life-changing products.
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The Quality Assurance (QA) Auditor II will have experience and knowledge of appropriate GxP compliance and other applicable regulations and laws, Parexel procedures and appropriate Parexel processes, which allows the individual to plan and conduct internal and external audits independently, or with minimal supervision.
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This position will support the customer quality team by reviewing and responding to warranty replacement requests and product safety and liability claims through resolution, fielding and discussing technical issues, answering questions from customers, sales colleagues, teammates and suppliers of our products and status of warranty claims.
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Implement electronic Quality Systems, such as eQMS, EDMS, and LMS, providing procedures and training for employees to effectively use the electronic Quality Systems. Work directly on technical investigations relating to Product Quality Complaints.
$120,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Identify and resolve issues in the manufacturing of Class III PMA medical device products, by designing and conducting Quality Engineering investigations, and working directly with manufacturing engineering, operators, and other plant personnel.
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Title: quality Company: Lfb Usa in North Reading, MA
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