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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Boston, MA client site.
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The QA Associate will support quality operations activities for the manufacture of cellular therapy products. BS/BA in a science/engineering field and a minimum of 3+ years working in Quality, with experience in cell therapy (or applicable) environment preferred.
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For these cell therapy developments, large numbers of PBMCs sourced from a single donor are important for creating relevant biological assays, as well as for quality control testing. Assemble, restock, perform quality control, and maintain supplies and equipment in a state of readiness to maintain a clean, safe, and efficient work environment.
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The role will support the GMP-validation of assay-automation in a fast-paced Quality Control laboratory located in Cambridge, Massachusetts. We are seeking an Sr. Specialist, QC Automation, to support the transition of GMP release and stability assays onto automated platforms for cell and gene therapy products.
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Minimum 3 years of clinical research, public health research experience or research working with high-risk patient populations.
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They will be able to interact fluidly with peers and supervisors in Manufacturing, and cross-functionally with Quality Control, Manufacturing, Logistical and Process Development Technology Transfer counterparts.
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Leads the oversight of wholesale credit risk in functional areas and business lines that encompass underwriting, independent risk management, credit review, rating practices and methodology, credit reserves practices and asset quality assessments.
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They empower consumers to be in control of their decisions for long-term care. Continuous Quality Improvement: We honor the fact that each of us is human, and we embrace a desire to examine the value and quality of our work and ask how we can provide a higher quality of service.
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7 + years of experience in Quality Control in GMP environment, Quality Control Investigations Lead will primarily be responsible for supporting late phase and commercial quality control activities.
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Experience writing change controls for biotech (biologics preferred) in an electronic Quality Management System such as Veeva or Trackwise. Work with technical SMEs (Regulatory, Engineering and Facilities, Manufacturing Science and Technology, Process Development, Supply Chain, Validation) to ensure the appropriate stakeholders are involved in the assessment of the change control and completion of the tasks.
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Working knowledge and/or ownership of the following quality systems: Change Control, CAPAs, Deviations, and Self inspection auditing, QA reporting and approval of GMP documentation. Promote a quality mindset and quality excellence approach to all activities.
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Ability to initiate, manage, and close quality systems such as change control, CAPA, and deviation management. Oversee the delivery of validation in complex, capital projects, ensuring adherence to engineering, quality, and compliance standards.
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Complete incoming inspection of components with the CFS Quality Assurance and Quality Control team. Inventory Control Specialist. Required Experience: 3+ Yrs Inventory Control; and 2 Yrs ERP Experience.
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You will be accountable for the implementation and support of products, inclusive of implementation and launch of new products, defect management, prioritization, and system support and quality control.
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Knowledge and understanding of software development processes with an appreciation for maintaining a high-quality bar with low operational overhead. 5+ years experience in Property Insurance product design and underwriting concepts.
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quality control jobs Title: specialist in Cambridge, MA
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