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Regulatory Affairs Labeling is a core function within Gilead's Global Regulatory Affairs organization and acts as a critical strategic partner across cross-functional teams.
$347,380 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Collaborate and work cross-functionally with Manufacturing, Regulatory Affairs, Assay Development, Finance, and Quality functions to ensure all activities are scheduled and executed on time in accordance with program timelines.
$225,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Duties:Provide expert legal advice and guidance on FDA regulatory requirements and compliance for drug, biologics, cellular, and gene therapy products. Firm Type: Law Firm, Experience: 10 Years, A law firm based in Palo Alto is seeking a highly experienced Senior FDA Drug/Biologics Regulation Counsel to provide comprehensive legal support in FDA regulatory matters pertaining to drug and biologics development.
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Associate Director, Public Affairs, US HIV Prevention Communications. Collaborate on programs related to HIV in other Public Affairs and Government Affairs teams and centers of excellence, including corporate communications, community engagement & advocacy, corporate giving, and government affairs.
$230,230 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Compliance requirements and guidelines for DMH, DPH, OSHA, NFPA, IBC, MWRA / EPA, and other regulatory agencies not specifically listed. The Director of Facilities Maintenance is responsible for compliance inspections and adheres to all safety, life safety, and equipment management programs as required by the Joint Commission and other applicable regulatory agencies.
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The Associate Director of Real-World Evidence (RWE) will provide scientific and strategic leadership for RWE using administrative claims data/EMR, reporting to the Head of Medical Affairs Statistics, Epidemiology and RWE. The Associate Director of RWE will function on a team responsible for establishing rigorous assessments of administrative claims data/EMR to evaluate real-world outcomes for all Jazz products.
$246,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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The Senior Manager, CMC Regulatory Affairs is a hands-on and independent role requiring a strong individual who will provide strategic and operational support to multiple programs, with an emphasis on CMC (Chemistry, Manufacturing, and Controls.
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Comprehensive knowledge of GCP, GLP, GMP and other regulations for pharmaceuticals, along with an understanding of global quality standards and regulatory authority inspection trends in relation to product development and commercialization.
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We are looking for someone that is highly motivated in their career growth (possible vertical and horizontal growth to take on wider roles as well such as Regulatory Affairs); must be a self-starter, team builder, and excellent in communication.
$235,600 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Head of Legal will report to the CEO and be responsible for providing legal counsel and support to Orca Bio on a wide range of matters, including corporate governance, strategic and financing transactions, contract operations and review, clinical trials, employment, regulatory compliance, and commercial preparedness.
$250,000 a yearExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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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Training and Knowledge Sharing: Educate internal teams about legal matters related to the ad tech industry, including regulatory compliance, intellectual property, data protection, and contract best practices.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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12+ years of work experience in a highly regulated industry as a regulatory affairs professional (e.g., Medical Devices, Bioengineering, Pharma, LifeSciences) Reality Labs is seeking an experienced medical devices regulatory affairs professional to lead the regulatory strategy and product approvals for novel hardware and software as a medical device products for distribution into many worldwide markets.
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Title: Vice President of Quality Assurance & Regulatory Affairs. Experience with FDA and EU MDR regulatory processes. Additionally, in this role you will coordinate and work with a number of outside regulatory consultants to implement Neptune’s regulatory strategy across its diverse product lines.
$325,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Interact with document authors, contributors, and reviewers (including members of Biometrics, Clinical Operations, Clinical Development, Project Management, CMC, Drug Safety, and Regulatory Affairs) to acquire necessary input into documents.
$190,000 a yearFull-timeExpandApply NowActive JobUpdated Today
regulatory affairs jobs Title: regulatory affairs manager Company: Baxter in Foster City, CA
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