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Stay informed about industry trends, best practices, and regulatory changes related to community engagement in the renewable energy sector, and ensure the team remains up-to-date. Represent the organization at community meetings, events, and forums, serving as a spokesperson and advocate for renewable energy development.
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We collaborate across the company to advance blockchain projects, enhance our products (including hardware devices, wallet apps, and Proof of Personhood), and ensure regulatory compliance in areas such as securities, AML/CFT, consumer protection, trade, IP, and labor.
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Certified Anti-Money Laundering Specialist (CAMS), Certified Fraud Examiner (CFE), or equivalent is a plus or willingness to obtain within one year. About You:5+ years of experience working in Financial Crime Compliance or paralegal, especially at a financial institution, e-Money/payments company, law firm, or other FinTech.
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Maintain cutting edge knowledge of best regulatory practices, quantitative/clinical pharmacology methodology, and drug development precedent. Serve as lead author and key contributor to clinical pharmacology sections of clinical and regulatory documents.
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The successful candidate will oversee and direct all Quality Unit functions (QA, QC and Quality Systems) and collaborate with internal business partners (including Manufacturing, Supply Chain, Process Development, Regulatory Affairs) to deliver the innovation pipeline and meet business targets.
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Extensive knowledge of drug development (Non-clinical, clinical, and CMC aspects), global pharmacovigilance principles, commercialization, and safety escalation governance processes, global regulatory authority operations, global regulatory agency submission process, technical skills (such as Microsoft Outlook, Word, Excel, PowerPoint); and working globally.
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Knowledge of fintech industry trends, competitive landscape, and regulatory requirements is a plus. More than 1,300 customers, including 23andMe, Bose, Boston Red Sox, Five Guys, and Zappos, rely on Planful to accelerate cycle times, increase productivity, and improve accuracy.
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Responsible for product compliance (food safety, ingredient usage, NLEA information, product claims) against internal and external standards (FDA, USDA, and third-party certification) through collaboration with regulatory, QA, marketing, and other parties.
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Coordinates performance improvement efforts, risk management, patient safety, regulatory compliance and infection prevention and control programs and activities within the SFHN so that teams work effectively to meet organizational and strategic priorities.
$289,380 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Applicants must be experienced in both advising on legal issues related to creative production and have experience in payments or financial institution marketing, applying knowledge of the FTC and CFPB rules and regulations and the current legal and regulatory framework.
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Working knowledge of laws, regulations and professional standards affecting case management practice in an integrated delivery system: including but not limited to CMS, Title 22 CHA Consent Manual, CDPH and The Joint Commission (TJC)A broad knowledge base of post-acute levels of care and associated regulatory compliance requirements.
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For your assigned portfolio, you will partner with the Relationship Manager to onboard new accounts and funds; service day to day deposit needs; triage complex deposit, liquidity, and digital channel inquiries; provide ongoing risk monitoring, address operational risk activity, and ensure consistent application of Group Policy and regulatory, financial, and legal standards.
$175,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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APAC Regulatory Specialist (China, Japan, Korea, Australia, Singapore). Role : Regulatory Specialist II- APAC. Familiarity with international regulatory standards and experience with APAC countries.
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Excellent written and verbal communication skills, with respect to both regulatory analysis for a lawyer audience and high-level synthesis for a Client audience; preferred candidates will submit writing samples demonstrating one or both styles.
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Author appropriate CMC sections to support regulatory filings (IND, IMPD, NDA, MAA) submissions as needed. Experience authoring and reviewing documents in support of CMC development activities and regulatory submissions (IND/IMPD, information requests, amendments, briefing books, NDA/MAA, etc.
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regulatory job in Oakland, CA
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