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Job ResponsibilitiesConducts quality assurance reviews of animal resource program and laboratories to monitor and ensure compliance with federal, state, institutional and departmental regulations.
$70,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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She/he is responsible for maintaining OASAS regulatory compliance and assuring that programs operate in accordance with Odyssey House organizational standards. Conduct utilization review, incident management and review and quality assurance reviews.
$80,000 a yearExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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The Quality Assurance Team is responsible for ensuring that Corporate Audit activities comply with internal policies and procedures, as well professional standards set forth by industry and regulatory institutions.
$154,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Execute Quality Assurance / User Acceptance Testing for each campaign launch, in partnership with marketing strategist, Salesforce Marketing Cloud Architect, data science and data engineer team members.
$43 an hourExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Technical and /regulatory issues may involve civil engineering, permitting including, but not limited to, drilling, and soil excavation/grading/disposal CEQA & NEPA compliance, NPDS compliance, CalOSHA regulations, and right of way permits.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Working closely with the VP of Quality, Director of Quality Control, and Senior Director of Operations you will lead strategy and direction of the QA function to ensure that manufacturing operations and QC testing are being performed and documented in compliance with global health authority regulations and expectations, as well as INCOG procedures.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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5+ years of hands on experience with Quality Management System including Electronic Document Management System (Veeva preferred), managing documents lifecycles-Draft to Effective/approved, Initial to Final and Periodic ReviewThorough understanding of Regulatory compliance requirements for the US FDAAuditor training/experience or certificationStrong understanding of risk assessment and risk management fundamentals/tools ·Knowledge of FDA, EU, ICH requirement for GMP and related areas.
$1 - $2ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Develop and manage a risk-based Quality Management System for QA in compliance with applicable regulatory requirements (US) and company policies. The Associate Director, Quality Assurance will be based in our Northern New Jersey, offices 1 - 2 days a week (flexible schedule for the ideal candidate.
$1 - $2ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Supervisor is responsible for maintaining OASAS regulatory compliance and assuring that programs operate in accordance with VIP Community Services organizational standards. · Ensure compliance with all referent communications, HRA STARS reporting, and HRA finger imaging verification.
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Key Responsibilities Provide quality leadership, strategy, and compliance oversight to CDMOs, CMO, CRO, CPO, Third Party Vendors. Ensure that CMC quality systems, validation, product specifications, product release, reference standard and stability programs are phase appropriate, effective, meet standards expected by US and global regulatory authorities.
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Associate Director-Quality Assurance (QCMC) Company is seeking a highly experienced, motivated, and innovative quality leader with strong experience in early and late-stage development to join our Quality team as Associate Director, Quality Assurance to support drug development from Phase 1 to late-stage development.
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Performs disposition activities for manufactured products in support of clinical products, including MBR, EBR review, and approval and review of CoA. Responsible for Management and maintenance of the Veeva Quality Docs System, including document drafting/Authoring, reviewing, approving, and finalizing internal quality documents (SOPs, Wis, Policies, Forms, etc.
$1 - $2ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This individual will partner with CMC, Clinical, Regulatory Affairs, and other corporate stakeholders to ensure Company’s clinical and commercial products follow cGMP framework and guidelines. ·Performs assessments and QA review of source documents, change controls, deviations, quality events, CAPA, root cause analysis, product impact assessment, investigations, including OOS investigations and other reports for accuracy.
$1 - $2ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform quality review of analytical documentations for CMC programs, including method transfer, qualification, validation protocol, in-process controls, data packets, CoA, and stability protocols/reports.
$1 - $2ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A minimum of three years of financial crimes (i.e., AML/OFAC/Anti-Bribery and Corruption (ABC)/Anti-Fraud) compliance or corporate intelligence or due diligence experience in the financial or professional services industries and/or with relevant banking/securities regulatory agencies.
Full-timeExpandApply NowActive JobUpdated 12 days ago
quality assurance regulatory compliance jobs in Brooklyn, NY
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