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This is a highly collaborative role and will work closely with The Customer Service, Clinical Operations, Provider Network Operations and Compliance and Regulatory Affairs Departments. Present grievance and appeals data to key stakeholders through Grievance Review Committee (GRC) and the Grievance Program Leadership Team (GPLT) as needed.
Full-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Working hand-in-hand with R&D, Regulatory Affairs, Legal, and Brand teams, they make sure all scientific communication is spot-on and compliant. Collaborate with the R&D, Regulatory Affairs, Legal, and Brand teams to ensure alignment on product claims and scientific communication.
$86,000 a yearExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Our full range of advisory services includes strategic communications, investor relations, financial transactions and restructuring, management consulting, physical and cyber risk, organizational design, board and executive search, geopolitics and government affairs, corporate governance, ESG and DE&I.
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1-3 year of experience in a scientific affairs or related role in the nutraceutical industry/space. Knowledge of regulatory requirements for product claims in dietary supplements preferred.
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Support the negotiation, execution, and management of contracts for other Nurix business teams (e.g., research and development, information technology, regulatory affairs, etc.) Contribute to special projects as assigned by the Contracts Counsel or Chief Legal Officer.
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Create and lead development strategies for Pattern Energy’s new and core markets in clean energy, transmission, green fuels and storage;Identify, evaluate and analyze potential changes in the competitive landscape which may enhance or detract from the business case for core North American strategies Provide insight on policy positions that Pattern's industry allies and internal political and regulatory affairs team should be taking to position Pattern favorably within changing market conditions.
$160,000ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Develop and maintain a roadmap of all potential customer, collaborator and partnerships to maintain a healthy, growing and diversified revenue pipeline Understand and effectively engage a wide range of internal and external resources including Legal, IP, Finance, R&D, Regulatory Affairs, Operations, Sales & Marketing, in order to develop and maintain effective customer-related, collaborations and partnerships for libraries and antibody development solutions.
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Identify, develop, and implement best practices for working/communicating with cross-functional leadership from partners such as Commercial, Global Medical Affairs, Regulatory Affairs, Research and Early Development, Market Access, Corporate Communications, Investor Relations and GPAE's cross-functional Global Advocacy & Partnerships Teams (APTs) and Regional Patient Engagement Teams (PETs) on ongoing, shared regional PAG-related activities.
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Regulatory Affairs Specialist III (Current Employee) Hercules, CA. The Senior PCR Production Chemist responsible for the fermentation, purification, and formulation of materials used in PCR Production.
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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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Department Description The Department of Quality & Safety consists of Adult Quality & Safety, Benioff Children’s Hospitals (BCH) Quality & Safety, Hospital Epidemiology & Infection Prevention, Regulatory Affairs, Health Equity, and Clinical Documentation Integrity.
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In this role as a Regulatory Affairs Specialist, you will have responsibility for developing and influencing regulatory policy and determining and pursuing courses of action necessary to obtain and expand regulatory approval of Hinge Health's medical device portfolio.
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Ability to engage, coach, and teach cross-functional team members regarding Regulatory Affairs and medical device requirements. Draft and execute regulatory strategies for new product development and device modifications, including identifying regulatory risks, tracking timelines and submission deliverables, and establishing contingency plans.
Full-timeExpandApply NowActive JobUpdated 2 months ago - UpvoteDownvoteShare Job
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Work is completed in close collaboration with the regulatory affairs, manufacturing, operations, and QC groups. The Quality Assurance Specialist will, with the guidance of the program Head of QA, perform quality assurance activities for the Investigational Cellular Therapy Group, UCSF HICTF and GMP Facility, and the Pediatric Cellular Therapy Laboratory.
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Minimum of 5 years of experience in patient advocacy and engagement, medical affairs, public health, and coalition building with a strong preference for experience in kidney disease patient advocacy.
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regulatory affairs jobs in San Francisco, KS, Arizona
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