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8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer. Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions.
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The College seeks a Provost and Executive Vice President for Academic Affairs ("Provost") who is a dedicated academic leader with a keen sense of the pressures facing higher education and proven ability in fostering innovation, building strategic partnerships, and supporting faculty excellence.
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Global Corporate Controllers (GCC) is responsible for overseeing the accounting, financial and regulatory reporting for the Firm. GCC prepares external financial reports for public filings and regulators.
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At least three years' experience working in student affairs in a higher education setting, ideally as a Dean or Associate Dean of Students. Collaborating with Law School faculty as well as numerous departments, including Academic Success, Operations, Career Services, Alumni Affairs, Campus Safety and Equal Opportunity and Title IX.
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The Certifications Regulatory Affairs Manager will own and oversee the maintenance of third-party certifications. Minimum of 5 years experience in the food industry, primarily in regulatory affairs, regulatory compliance or technical related fields.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Conduct planning, execution of Mizuho’s Regulatory Reporting Quality Assurance Program with various regulatory reports, especially broker dealer regulatory reports such as FOCUS, SSOI, OBS reports.
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CFR also publishes Foreign Affairs , the preeminent magazine on global issues, and provides up-to-date information about the world and U.S. foreign policy on its award-winning website, CFR.org.
$62,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Provides orientation and boot camp training which includes new topics in coding (inpatient and outpatient), chart review, reimbursement and regulatory changes. NYC Health + Hospitals is the largest public health care system in the United States.
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10+ years of pharmaceutical/biotech drug development experience with 5+ years of experience in global CMC regulatory affairs with working experience and content knowledge in CMC development of NCEs and small molecules.
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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. Qualified Mental Health Professional (e.g., LCSW, LMSW, LMHC, CRC, Ph. D., MSN, CASAC, etc.
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Must be and remain compliant with any and all regulatory requirements for working in the cannabis industry. The Dispensary Associate is responsible for guiding customers through the cannabis purchasing experience, making informed recommendations based on customer's desired outcomes, provide informed and accurate descriptions of our products, and operate with a high level of accuracy in a fast-paced environment.
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This role involves working closely with IT, security teams, and business units to ensure that our cyber risk posture is aligned with our business objectives and regulatory requirements. CPA, CA, CISA, CISSP, CISM, CBCP, CIA, CIPP, CGEIT certification is desired; non-certified hires are required to become certified to be eligible for promotion to Manager.
$154,700 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Student Leadership: Work with Faculty and Academic Affairs to create opportunities for student engagement, learning, and leadership development as part of the work within the strategic partnerships.
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6-8 years of relevant experience in the biopharmaceutical industry, with at least 5 years focused on CMC Regulatory Affairs for biologics. Experience in managing interactions with regulatory health authorities and submitting CTA/IND and BLA/MAA filings, particularly related to gene therapy.
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Collaborate with other organizational departments responsible for functional aspects of the HIV Special Needs Plan, including, but not limited to Integrated Care Management, Behavioral Health, Managed Long-Term Care, Utilization Management, Quality Management, Credentialing, Regulatory Affairs, Compliance, Corporate Affairs, Provider Network Operations, Medicare Services, Information Systems, Finance, Claims, and Member Services and Eligibility.
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regulatory affairs jobs Title: regulatory affairs Company: Baxter in Ridgefield, NJ
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