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Algonquin Power & Utilities Corp. is a growing renewable energy and utility company with over $15 billion of assets across North America and internationally.. For more than 30 years, Algonquin has demonstrated an unwavering commitment to delivering clean energy and water solutions.. Our rapid growth has led both our regulated utility services and renewable energy business groups into different geographies and commodities, but our purpose remains unchanged – Sustaining Energy and Water for Life. Through our operating business (Liberty), we provide regulated electricity, water, and natural gas utility services to over 1 million customer connections, primarily in North America.. And, our growing portfolio of clean, renewable wind, solar, hydro and thermal power generation facilities represent over 3 GW of renewable generation capacity in operation and under construction.
The ideal candidate will hold a Juris Doctor (JD) and have a strong background in navigating complex regulatory frameworks, with direct experience engaging federal agencies such as the National Highway Traffic Safety Administration (NHTSA), Environmental Protection Agency (EPA), and Federal Trade Commission (FTC). Serve as a key advisor on federal regulatory and legislative matters, particularly related to automotive regulation, transportation safety, environmental policy, and consumer protection. Juris Doctor (JD) from an accredited law school. Capitol Hill, federal agency, or in-house corporate government affairs background. Please send your resume and cover letter to: Lea Diamond, Senior Vice President of People Operations at autocarejobs@autocare.org.
We believe that blockchain and digital asset innovation will transform how value moves through the world and were building the products and services to make that future a reality.. Our institutional digital assets platform spans trading, investment banking, asset management, staking, self-custody, and tokenization technology.. Led by CEO and Founder Michael Novogratz, our team blends deep crypto expertise with institutional experience and a shared commitment to shaping the future of Web3 and AI. In addition to ensuring compliance, you will attend Independent System Operator (ISO) or Public Utility Commission (PUC) stakeholder meetings, workshops, and discussions to advocate for Galaxys position within the relevant market.. Direct, recent experience within the ERCOT and PUCT stakeholder environment
Fate Therapeutics is looking for an Executive Director or Senior Director in Regulatory Affairs to oversee and direct the strategic planning and execution of clinical regulatory activities essential for initiating and conducting clinical trials and securing regulatory approvals. Provide strong cross-functional leadership for global filings including authoring/reviewing sections of IND/CTA, NDA/BLA/MAA, and other global submission documents in support of clinical trials and marketing applications, as well as their amendments, in conformance with local regulatory requirements. Provide mentorship and oversight of Regulatory Affairs staff to plan, manage, author, coordinate, and review regulatory submission documents and development activities to support regulatory filings and dossier lifecycle. Qualifications BS/MS/PhD degree in a life science with at least 12 years of progressive experience in Regulatory Affairs in the biotechnology or pharmaceutical industry. Previous cell therapy product experience and regulatory knowledge is highly preferred.
Nura Bios research and early development small molecule pipeline focuses on halting axon degeneration and/or modulating microglial responses to degeneration and injury, with the goal of conferring neuroprotection across diseases of the central, peripheral, and ocular nervous system.. The VP/Head of Regulatory Affairs will be a key member of our clinical leadership team, responsible for developing and executing regulatory strategies to support the company\'s product development and commercialization goals.. Lead interactions with regulatory agencies, including the FDA, EMA, and other global health authorities, to facilitate the approval process.. Advanced degree in a relevant scientific discipline (e.g., PharmD, PhD, MD).. 12+ years of experience in regulatory affairs within the pharmaceutical or biotechnology industry.
Directly manages the team responsible for following: CMS enrollment, Medicaid enrollment, state licenses, Joint Commission accreditation, payor contract review, and quality systems.. Leads organization through all activities required to maintain Joint Commission accreditation.. Acts as a Contract Administration lead and be able to train new hires.. Experience and competency with EMR systems, Government and Insurance Portals.. Experience with regulations pertaining to being a service provider for durable medical equipment (DME) and / or an independent diagnostic test facility (IDTF) strongly preferred
We are seeking a Group Vice President, Legal Affairs to serve as a broad-based utility player and trusted business partner to our General Counsel and executive team. This is a generalist role designed to provide coverage across core in-house legal needs, allowing company to thrive, legal department to excel, and the business to move with confidence. Insurance: Oversee corporate insurance programs and claims management. Proven ability to support and amplify the GC while operating independently when needed. Opportunity to shape legal strategy at the intersection of health, fitness, and consumer products.
Director of Environmental & Regulatory Affairs reports to the Chief Operating Officer for US Operations. This role provides strategic direction for the environmental performance of WML by developing, implementing, and monitoring environmental strategies that promote sustainable development for US operations. Research, design, develop, and evaluate plans to protect or improve air, soil, and water quality. Bachelors degree from an accredited college or university with a major in Business Administration, Environmental Science, Planning or a related field. To assist you in leveraging the health care benefits, we offer personal health advocates, tele-medicine, surgery concierge services, diabetes care.
Aypa Power, a Blackstone portfolio company, is a leading developer, owner, and operator of utility-scale energy storage and hybrid renewable projects that power our communities and cities.. We have been at the forefront of energy storage development since our first energy storage project came online in 2018.. As a leader in our industry, we have over 22 GW of utility-scale energy storage and hybrid renewable energy projects in development and 33 projects in operation or construction across North America.. We are seeking a strategic and experienced Senior Director of Government & Regulatory Affairs to lead state and local engagement across key Midwest and Eastern markets, ensuring our portfolio of energy storage and hybrid renewable projects through evolving political, policy, and regulatory environments.. Monitor and influence legislative and regulatory proceedings impacting energy storage and project siting;
- Unlimited vacation, supportive parental leave policy, and company-wide holiday shutdown.. Lead and evolve Kepler’s global spectrum strategy, including frequency planning, global market access, ITU coordination, and other national or international licensing. Secure and protect spectrum assets to support growth of Kepler’s LEO constellation, inter-satellite links, and future innovation in optical and lunar relay systems. 10+ years in spectrum management, regulatory affairs, or telecom law within the satellite or aerospace sector. Technical expertise in RF engineering, satellite systems, and/or inter-satellite links
Join to apply for the Head of Regulatory Affairs US & Canada role at Greiner Bio-One Americas. Developing and implementing regulatory submission strategies in collaboration with R&D and Product Management. Coordinating Field Safety Corrective Actions and reporting to authorities. 10+ years of experience in FDA regulatory affairs and medical devices. Knowledge of international quality standards (ISO, cGMP)
Head of Regulatory Affairs US & Canada. Coordination of Field Safety Corrective Actions and authority reporting. Master’s degree in a relevant life-science or engineering field. Proven experience in international FDA regulatory affairs (10+ years). In-depth knowledge of international quality standards and regulatory requirements (ISO and cGMP)
Unlike traditional cold-storage methods, the OCS Systems feature warm, normothermic perfusion, and provide the means to monitor organ health so that transplant patients can experience better outcomes. Prepare regulatory submissions for the FDA, including PMA and IDE applications, supplements and reports and 510(k) submissions.. Solid experience and proven track record in successful FDA submissions including IDE and PMA applications, supplements and reports. Director Global Regulatory Affairs - Precision Medicine and Digital Health.. Senior Director, Global Regulatory StrategySenior Director, Regulatory Affairs Advertising & PromotionSenior Director, Global Regulatory StrategyHead of Regulatory Affairs, Cell Therapy ImmunologySenior Manager / Associate Director, Regulatory Strategy - CMCDirector, Regulatory Affairs Advertising & Promotion
The Global Affairs team advances this mission by engaging with policymakers, regulators, and stakeholders worldwide to ensure a healthy, open, and innovation-friendly environment for storytelling and streaming.. With a growing content slate and new businesses in live events, games, and advertising, it is an exciting time to join the Netflix team.. Netflix is seeking a Senior Manager of U.S. Regulatory Affairs to join our UCAN team.. Develop high-impact advocacy materials, including policy strategy, regulatory and legislative analysis, talking points, presentations, and regulatory filings.. Familiarity with relevant Congressional committees, including House Energy & Commerce and Judiciary; Senate Commerce and Judiciary.
This position is responsible for providing guidance on regulatory affairs activities for Ipsen products under development in US, in collaboration with the head of Global Regulatory Affairs US lead and global therapeutics area leads.. The Head of US Regulatory Affairs & Quality will serve as a principal regulatory liaison to the FDA for all US affiliate activities during the product lifecycle.. Ethics & Compliance. Degree in life sciences; advanced degrees (PhD, PharmD, MD, MSc) preferred with regulatory and GxP experience.. 8-10 years in biopharma regulatory affairs or related fields.
We believe that blockchain and digital asset innovation will transform how value moves through the world - and we're building the products and services to make that future a reality.. Our institutional digital assets platform spans trading, investment banking, asset management, staking, self-custody, and tokenization technology.. Led by CEO and Founder Michael Novogratz, our team blends deep crypto expertise with institutional experience and a shared commitment to shaping the future of Web3 and AI.. In addition to ensuring compliance, you will attend Independent System Operator ("ISO") or Public Utility Commission ("PUC") stakeholder meetings, workshops, and discussions to advocate for Galaxy's position within the relevant market.. Bonus Points: Direct, recent experience within the ERCOT and PUCT stakeholder environment
Global Public Policy is responsible for Vantage Data Centers’ government relations, economic development, and community engagement.. The team partners with our New Site Development, Construction, Engineering, Legal, Tax, People, Operations, and other departments to grow market share, acquire and retain customers, navigate through regulatory and policy developments, mitigate risk, and expand into new geographies.. Support strategy development and advocacy around cost allocation, grid access, energy supply planning, and permitting reform. 3–5 years of experience in regulatory affairs, permitting, energy policy, or a related field. Community Relations & Mobilization Strategist Business Ops Specialist - ADMIN III - HYBRID. We’re unlocking community knowledge in a new way.
Title: Senior Specialist, Compliance and Regulatory Affairs. Reports to: Senior Director, Risk and Compliance. Location: Alexandria, VA preferred/Remote eligible if outside the DC metro area. Federal and/or State Government Agencies Occasionally. Assist other team members with continuous improvement of compliance/qualifications assessment review processes and procedures
Unlimited vacation , supportive parental leave policy, and company-wide holiday shutdown.. Key Responsibilities Lead and evolve Kepler’s global spectrum strategy, including frequency planning, global market access, ITU coordination, and other national or international licensing.. Secure and protect spectrum assets to support growth of Kepler’s LEO constellation, inter-satellite links, and future innovation in optical and lunar relay systems.. Required Skills & Qualifications 10+ years in spectrum management, regulatory affairs, or telecom law within the satellite or aerospace sector.. Technical expertise in RF engineering, satellite systems, and/or inter-satellite links.
Industry/Domain: Consumer Products – Regulatory Affairs, Compliance, Product Safety. We are hiring a highly experienced Principal Regulatory Affairs Specialist to oversee regulatory affairs activities for US consumer product categories.. Head of Private Credit and Alternative Investments New Haven, CT $127,200.00-$225,225.00 2 weeks ago. Head of Reporting and Technical Accounting Head of Product Development - Party Goods Vice President, Smilow Ambulatory and Radiation Oncology New Haven County, CT $115,000.00-$120,000.00 2 weeks ago. Supr Food Drive-Thru | Head of Operations Vice President, Smilow Ambulatory and Radiation Oncology Stamford, CT $130,000.00-$135,000.00 1 week ago