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Minimum of 5 years’ experience related to quality assurance, lean manufacturing, regulatory compliance, and Six Sigma manufacturing in a manufacturing environment; previous direct leadership experience preferred.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Complete all work in compliance with established cGMP, FDA, OSHA, USDA, EPA, ISO and Quality System regulations, as applicable, to assure output meets established quality and regulatory specifications.
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Facilitate in the development of documents, and update documents pertaining to lab procedures and product manufacturing to maintain cGMP and ISO compliance, and increase efficiency. The Mfg Lab Technician performs laboratory activities in the manufacturing lab including Buffer and antibody manufacturing.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Experience and understanding of various governance frameworks and standards such as COSO, COBIT, ISO, NIST, CMMC, GDPR. Looking for strong operations or accounting professional with critical thinking and process improvement skills, who can provide organizations with documented testing as walkthrough of process and internal controls and regulatory compliance.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Responsibilities Include: Conduct regulatory compliance audits and assessments utilizing frameworks like CMMC, NIST, CSF, ISO, PCI, HIPAA, etc. Review and deliver penetration testing and vulnerability scanning reports to clients.
$60,000 - $80,000 a yearFull-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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In depth knowledge performing risk management per ISO In depth knowledge in developing and testing products to IEC- Safety standard In depth knowledge in developing and testing products to IEC EMC standard Requirements: BS degree in engineering Understanding of US and international regulatory requirements for medical devices strongly preferred Experience developing reliability plans.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This team is looking for someone with a background in governance risk compliance, auditing, NIST, ISO, frameworks and controls. Ensure the risk management program incorporates cyber risk identification, measurement of potential losses, regulatory needs, mitigation, monitoring, reporting, and escalation process.
$100,224 - $127,476 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Comprehensive understanding of the regulatory environment including HIPAA/HITECH, PCI; and information security frameworks i.e. NIST, ITIL, FIPS, FISMA, ISO, and Cobit. Knowledge of health care trends, policy, regulatory, and compliance issues.
$44.64 - $52.45 an hourExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Preferably an experienced ISO Auditor. The Manager Regulatory Affairs & Quality Americas have responsibility for setting priorities and expectations among their direct reports and monitoring/reporting on budget, planning and logistics.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Regulatory and statutory requirements, as well as industry specific guidelines, such as PCI DSS, ISO. ctivities in accordance with regulatory and departmental policy and procedures.
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Practical experience in application of ISO standards and regulatory requirements within the In Vitro Diagnostic and/or Medical Device space (MDSAP, EU, and US regulatory requirements desired, additional geographies a plus.
$127,000 - $174,700 a yearExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Support the ongoing update of the QMS in line with emerging issues or changes to regulatory expectations. In depth knowledge of cGMP, cGDP, relevant ISO standards and medical device requirements.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Coordinate with sterilization facility to ensure routine revalidation and device testing is aligned with industry and regulatory requirements One project= in 2023 a couple chillers need to be installed b/w 23 and 24 (May is the plan) just need to investigate piping.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Perform work in accordance with NASA ISO AS9100 procedures and applicable regulatory requirements. Attention all talented Engineers with advanced Engineering principles understanding and leadership experience : AMERICAN SYSTEMS wants you to join our winning team as our next Principal Flight Systems Engineer at the NASA Armstrong Flight Research Center (AFRC) on Edwards AFB in California.
$130,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Senior Specialist Quality Assurance participates as a lead member of the Software Quality Assurance (SWQA) team for Abbott Diabetes Care products that ensures digital applications and firmware produced by ADC is developed, validated, and maintained in compliance with regulatory, corporate and divisional requirements.
$92,800 - $185,600 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago
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