Current jobs related to Manager, Regulatory Affairs - Texas City - The AES Corporation
-
Regulatory Affairs Executive
3 weeks ago
Texas, United States Talently Recruiting Full timePosition Title: Director of Regulatory AffairsLocation: San Antonio, TXCompensation: $140K - $160K+ based on experience, plus a performance bonus of 25%Required Expertise: Regulatory Affairs, Leadership, Medical Device Regulations, FDA ComplianceCompany Overview:We are a pioneering organization in the medical devices sector, focusing on regenerative...
-
Regulatory Affairs Executive
3 weeks ago
Texas, United States Talently Recruiting Full timePosition Title: Director of Regulatory AffairsLocation: San Antonio, TXCompensation: $140K - $160K+ based on experience, plus a performance bonus of 25%Required Expertise: Regulatory Affairs, Leadership, Medical Device Industry, FDA RegulationsCompany Overview:We are a pioneering organization in the medical devices sector, situated in San Antonio, TX,...
-
International Regulatory Affairs Manager
3 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a leading entity in the field of Interventional Pulmonology, specializing in innovative tools and therapies for Obstructive Lung Disease. Our commitment to excellence is exemplified by our flagship product, the Zephyr Valve, which has been recognized for its groundbreaking technology in the realm of...
-
Regulatory Affairs Manager, International
3 weeks ago
Redwood City, California, United States Pulmonx Full timeCompany OverviewPulmonx is a leading innovator in Interventional Pulmonology, Planning Tools, and Treatments for Obstructive Lung Disease. Based in the United States and Switzerland, Pulmonx is the manufacturer of the Zephyr Valve. The Zephyr Valve was granted breakthrough status and approved by the FDA in 2018, as it represents a breakthrough technology...
-
International Regulatory Affairs Manager
3 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a leading innovator in the field of Interventional Pulmonology, specializing in advanced tools and therapies for Obstructive Lung Disease. The company is recognized for its groundbreaking Zephyr Valve, which received breakthrough designation from the FDA due to its significant clinical advantages in lung...
-
International Regulatory Affairs Manager
3 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a recognized leader in the field of Interventional Pulmonology, specializing in innovative tools and therapies for obstructive lung diseases. Our flagship product, the Zephyr Valve, has received significant accolades, including breakthrough designation from the FDA due to its unique approach to lung volume...
-
Manager, Regulatory Affairs, International
2 weeks ago
Redwood City, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a Global Leader in Interventional Pulmonology, Planning Tools, and Treatments for Obstructive Lung Disease. Based in Redwood City, California, and Neuchâtel, Switzerland, Pulmonx is the maker of the Zephyr Valve. The Zephyr Valve was granted breakthrough status and approved by the FDA in June 2018,...
-
International Regulatory Affairs Manager
3 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a recognized leader in the field of Interventional Pulmonology, specializing in innovative planning tools and treatments for obstructive lung diseases. With operations in multiple global locations, Pulmonx is renowned for its Zephyr Valve, a device that received breakthrough designation from the FDA in...
-
International Regulatory Affairs Manager
3 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a leading entity in the field of Interventional Pulmonology, specializing in innovative solutions and therapies for Obstructive Lung Disease. The company is recognized for its development of the Zephyr Valve, a device that has achieved breakthrough status and received FDA approval due to its significant...
-
International Regulatory Affairs Manager
3 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeManager, Regulatory Affairs, InternationalPulmonx is a leading organization in the field of Interventional Pulmonology, offering innovative solutions and therapies for Obstructive Lung Disease. The company is recognized for its development of the Zephyr Valve, a groundbreaking device that received breakthrough designation from the FDA in June 2018, as it...
-
Texas, United States Removery Full timePosition Title: Manager of Medical Compliance and Regulatory AffairsABOUT REMOVERYJoin us in our mission to redefine the tattoo removal experience. Removery is a pioneering, collaborative organization specializing in laser tattoo removal, with operations across multiple countries. We are dedicated to making a significant impact in the lives of individuals...
-
Regulatory Affairs Director
1 week ago
Foster City, California, United States Gilead Sciences, Inc. Full timeJob SummaryWe are seeking a highly skilled Regulatory Affairs Director to join our team at Gilead Sciences, Inc. As a key member of our Global Regulatory Affairs organization, you will play a critical role in ensuring compliance with governing laws, regulations, and company policies while enabling the business to meet its goals and objectives.Key...
-
Regulatory Affairs Director
2 weeks ago
Redwood City, California, United States Adverum Biotechnologies Full timeAbout the RoleWe are seeking a highly experienced and skilled Regulatory Affairs Director to lead our CMC Regulatory strategy for Adverum's gene therapy program/s. As a key member of our team, you will be responsible for developing, executing, and advising on global Regulatory CMC strategies through all phases of our development program/s.Key...
-
Regulatory Affairs Director
3 weeks ago
Redwood City, California, United States Pulmonx Full timeAbout PulmonxPulmonx is a leading medical device company dedicated to developing innovative solutions for respiratory health. We are seeking an experienced Regulatory Affairs Director to join our dynamic team.Key ResponsibilitiesRegulatory Strategy Development: Develop and implement comprehensive regulatory strategies that align with company goals and ensure...
-
Regulatory Affairs Director
2 weeks ago
Redwood City, California, United States Pulmonx Corporation Full timeJob SummaryWe are seeking a highly experienced Regulatory Affairs Director to join our team at Pulmonx Corporation. As a key member of our leadership team, you will be responsible for implementing regulatory strategies worldwide to ensure compliance with regulatory requirements and obtain regulatory approval for our products.Key ResponsibilitiesRegulatory...
-
Regulatory Affairs Director
1 week ago
Redwood City, California, United States Adverum Biotechnologies, Inc. Full timeAbout the RoleWe are seeking a highly experienced Regulatory Affairs Director to lead our CMC Regulatory strategy for our gene therapy programs. As a key member of our team, you will be responsible for developing, executing, and advising on global Regulatory CMC strategies across all phases of our development programs.Key ResponsibilitiesRegulatory Strategy...
-
Regulatory Affairs Specialist
3 days ago
Daly City, California, United States Katalyst Healthcares and Life Sciences Full timeJob Title: Regulatory Affairs SpecialistAt Katalyst Healthcares and Life Sciences, we are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will be responsible for developing and implementing global regulatory strategies for medical device products.Key Responsibilities:Develop global...
-
Regulatory Affairs Specialist
2 days ago
Redwood City, California, United States REVOLUTION Medicines Full timeRevolution Medicines: A Leader in Precision OncologyWe are a clinical-stage precision oncology company dedicated to developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.The OpportunityThe Senior Associate, Regulatory Affairs will support Senior Regulatory Affairs management in day-to-day operational aspects of the...
-
Regulatory Affairs Specialist
7 hours ago
Redwood City, California, United States REVOLUTION Medicines Full timeRevolution Medicines: A Leader in Precision OncologyRevolution Medicines is a clinical-stage precision oncology company dedicated to developing innovative targeted therapies to combat RAS-addicted cancers. Our research pipeline focuses on RAS(ON) Inhibitors and RAS Companion Inhibitors, designed to suppress diverse oncogenic variants of RAS proteins and...
-
Director of Regulatory Affairs
1 week ago
redwood city, United States MFS Talent Full timeShift: Days - 8 hours, Monday-Friday, 40hrs/weekLocation: Onsite, Palo Alto, CACompensation: $180k-$230k annually Duties and ResponsibilitiesResponsible for strategic and operational regulatory input and support for collaboration with other project team members, including regulatory team members. Contributes to the development of regulatory plans and...
Manager, Regulatory Affairs
4 months ago
At AES, we raise the quality of life around the world by changing the way energy works. Everyone makes an impact every day in our small, global teams. Apply here to start an extraordinary career today.
AES Clean Energy, a subsidiary of The AES Corporation global company, specializes in developing, owning, and operating utility scale projects such as PV solar, PV solar combined with battery energy storage systems (BESS), stand-alone battery energy storage and wind generation. AES CE currently has more than 6,300 MW of solar, wind and storage projects in operation in the U.S., with an additional 4,800+ MW contracted or in development.
*Please note this role is primarily remote, but must be based in Houston, TX; Austin, TX or surrounding area.
The Manager of Regulatory Affairs at AES Clean Energy (AESCE) will be tasked with supervising AESCE's positions and fostering relationships within the Federal Energy Regulatory Commission (FERC), managing policy positions within Regional and Independent Transmission Organizations (RTO/ISO), and taking the lead on filings and policy positions at state Public Utility Commissions (PUC) or Public Service Commissions (PSC) in key states. the Manager of Regulatory Affairs will play a pivotal role in managing regulatory policy in Texas and other regions as AES Clean Energy expands its operations, ensuring compliance and alignment with evolving regulatory landscapes across various geographical areas. This role involves actively contributing to developing corporate strategies, policies, and plans that align with regulatory frameworks and market dynamics where AESCE operates. Moreover, the Manager will proactively identify potential policy changes or adaptations beneficial to the business and effectively communicate these insights to internal teams to formulate strategy. Cultivating and sustaining relationships with regulatory bodies, their personnel, relevant authorities, committees, and partner organizations will be crucial. The ideal candidate will possess a comprehensive understanding of AESCE's assets and products, exceptional communication skills, and a collaborative approach to partnership.
Primary Job Responsibilities:
• Manage AESCE's policy and filing priorities at FERC, the RTO/ISOs and state PUCs
• Liaise with other AESCE teams (Development, Origination, Markets) to understand policy impacts to projects and clean energy products.
• Develop regulatory positions and strategies to promote priorities and offset potential roadblocks to development and new products.
• Work with appropriate industry associations or NGOs to further AESCE's regulatory work.
• Provide updates on critical regulatory proceedings to Senior Leadership teams in a timely manner.
• Hire and lead regulatory consultants to assist policy priorities.
• Manage a regulatory budget.
• Coordinate policy priorities, relationship management and communications with AESCE Strategy Team.
• Some travel may be required.
Requirements:
• At least 5 years of experience in regulatory policy or with an ISO is preferred.
• An advanced degree in Engineering, Economics or a law degree and/or relevant ISO experience preferred. Sophisticated education, particularly at the post-secondary level, may serve as a viable substitute for professional experience. Candidates with advanced degrees or relevant academic credentials commensurate with the required experience will be duly considered.
• Experience in the energy sector with a preference for renewable energy experience.
• Strong experience and proven skills in understanding the regulatory process at state, RTO/ISO, and FERC. ERCOT experience preferred.
• Outstanding analytical skills in understanding policy impacts to energy development and pricing.
• Communication skills: ability to develop and deliver concise powerful messages verbally, in writing and in presentations.
• Unwavering ethics and strong moral compass in all transactions.
Personal Attributes and Traits:
• Passion to work in a company that is driving the transition to clean energy and the motivation and energy to support the achievement of our mission.
• Excellent interpersonal, written and oral communication skills.
• Self-starter that can excel in situations with ambiguity and evolving mandates.
• Ability to work collaboratively and effectively with multiple internal group members across different businesses and develop creative solutions.
• High level of intellectual curiosity and professionalism.
• Global mentality and comfort with working with people from multiple different backgrounds and cultures.
• Must be a great teammate, knowing that what we will build as a team will be better than what we would each build alone; "no task is beneath me" demeanor reflecting the fast-growing nature of the Clean Energy unit.
• Exemplify our Values of Safety First, Highest Standards, and All Together.
AES is an Equal Opportunity Employer who is committed to building strength and delivering long-term sustainability through diversity and inclusion. Respecting all backgrounds, differences and perspectives enables us to improve the lives of our people, customers, suppliers, contractors, and the communities in which we live and work. All qualified applicants will receive consideration for employment without regard to sex, sexual orientation, gender, gender identity and/or expression, race, national origin, ethnicity, age, religion, marital status, physical or mental disability, pregnancy, childbirth, or related medical condition, military or veteran status, or any other characteristic protected under applicable law. E-Verify Notice: AES will provide the Social Security Administration (SSA) and if necessary, the Department of Homeland Security (DHS) with information from each new employee's I-9 to confirm work authorization.
AES is an Equal Opportunity Employer who is committed to building strength and delivering long-term sustainability through diversity and inclusion. Respecting all backgrounds, differences and perspectives enables us to improve the lives of our people, customers, suppliers, contractors, and the communities in which we live and work. All qualified applicants will receive consideration for employment without regard to sex, sexual orientation, gender, gender identity and/or expression, race, national origin, ethnicity, age, religion, marital status, physical or mental disability, pregnancy, childbirth, or related medical condition, military or veteran status, or any other characteristic protected under applicable law. E-Verify Notice: AES will provide the Social Security Administration (SSA) and if necessary, the Department of Homeland Security (DHS) with information from each new employee's I-9 to confirm work authorization.
#J-18808-Ljbffr
