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Utilizing knowledge and understanding of cGMP (Current Good Manufacturing Practices), ISO standards, and the company's Quality Management System, the Facilities Engineer will oversee the coordination, compliance, and documentation requirements for all facilities projects.
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Understands and utilizes the Quality Improvement tools for improvement and Risk Management Theory for improvement. Utilizes the Quality Improvement methodology for monitoring and Performance Improvement.
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We are seeking a quality control professional from the chemicals, pharmaceutical, or biotech industries to assist in the analysis and verification of a range of flow battery electrolyte samples.
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Organized, self-motivated, and capable of working independently or in a collaborative environment Excellent written and verbal communication skills Experience in supporting scale-up and technology transfer to pilot or commercial scale facilities Experience in a research laboratory setting, a strong background of traditional bioprocessing, and/or a working knowledge of cGMP (current Good Manufacturing Practices.
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The individual in this role will perform cGMP QC sample management activities for QC Chemistry, Microbiology, Bioassay, and various Development labs. Seeking a contract role in Quality Control Sample Management Associate II based at their Norwood, MA site.
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The Staff Supplier Quality Engineer serves as ABIOMED’s primary technical contact with all US based suppliers, leads all product development team’s supplier initiatives, second source critical suppliers, and establishes “Quality at the Source” programs with key partners.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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Job Title: CMM Programmer Job Code: 10632 Job Location: Wilmington, MA Job Description: Responsible for performing inspections, tests and/or audits of purchased parts, units, materials, equipment, panel/module level assemblies and quality control programs to specifications.
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Support the performance of the other appropriate Quality Assurance functions including document writing/revisions, deviations, CAPA's, document/data review and other administrative duties as needed.
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The Quality Control Laboratory Support Technician (RP/ISO) is responsible for inventory management, glassware cleaning, and basic equipment verifications within the Quality Control department.
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Complete cGMP documents as required and assist site and corporate Quality Assurance including, but not limited to: Investigations Corrective and Preventative Actions Deviations Out of Specifications No or Atypical Yields Manufacturing and QC Records Logbooks · Write and review internal procedures.
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SCM Order Mgmt, Service/RMA, Direct/Indirect Procurement, Product Mgmt, Quality, Inventor. Must have experience with Order Mgmt, Service/RMA, Direct/Indirect Procurement, Product Mgmt, Quality, Inventory.
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University or technical college degree or equivalent qualification in relevant sciences such as: Medicine, Pharmacy, Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Health Technology, Toxicology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology, Human Physiology, Nursing, Quality Management.
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DCF works toward establishing the safety, permanency and well-being of the Commonwealth's children by: stabilizing and preserving families; providing quality temporary alternative care when necessary, safely reunifying families; and when necessary and appropriate, creating new families through kinship, guardianship or adoption.
$76,176.62 - $103,533.04 a yearFull-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Leadership in areas of Lean Manufacturing, KAIZEN, ISO quality systems, innovation, and current systems technology. Efficient setup and operation of a flexographic press, focusing on meeting specifications in product quality, safety, and effective management of material and product waste.
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HemaCare's vertically integrated solutions support preclinical research, clinical studies from phases 1 to 3, and commercialization with high-quality RUO and GMP-compliant starting material and apheresis collections.
$39.86 - $49.23 an hourFull-timeExpandApply NowActive JobUpdated 12 days ago
cgmp quality jobs Company: Randstad Usa in Andover, MA
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