Occupational Therapist - $76K-82K per year Select MedicalOccupational Therapist - $76K-82K per yearDallas, TX$75,920–$81,848 / yearSelect Medical is one of the largest operators of critical illness recovery hospitals (previously referred to as long term acute care hospitals), rehabilitation hospitals (previously referred to as inpatient rehabilitation facilities), outpatient rehabilitation clinics, and occupational health centers in the United States based on the number of facilities. Select Medical operated 100 critical illness recovery hospitals in 28 states, 28 rehabilitation hospitals in 12 states, and 1,695 outpatient rehabilitation clinics in 37 states and the District of Columbia.
Family Nurse Practitioner / Physician Assistant-Float Fast Pace HealthFamily Nurse Practitioner / Physician Assistant-FloatBurkeville, TXPosting Title: Family Nurse Practitioner / Physician Assistant-Float Overview: In a manner consistent and supportive of our values, the Provider is responsible for delivering high quality health care within Fast Pace Health’s scope of services while achieving optimum patient satisfaction. They must have the ability to respond quickly and accurately to changes in condition or response to treatment and is responsible for providing outstanding patient service within the clinic and through various virtual communication channels, while maintaining a compassionate and welcome atmosphere.
["Senior Regulatory Affairs Manager","Senior Regulatory Affairs Manager"] Medtronic plc["Senior Regulatory Affairs Manager","Senior Regulatory Affairs Manager"]Fort WorthThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Family Nurse Practitioner Fast Pace HealthFamily Nurse PractitionerJasper, TXThey must have the ability to respond quickly and accurately to changes in condition or response to treatment and is responsible for providing outstanding patient service within the clinic and through various virtual communication channels, while maintaining a compassionate and welcome atmosphere. Posting Title: Family Nurse Practitioner Overview: In a manner consistent and supportive of our values, the Provider is responsible for delivering high quality health care within Fast Pace Health’s scope of services while achieving optimum patient satisfaction.
Manager Regulatory Affairs Just Energy Group IncManager Regulatory AffairsAustin, TXRemoteReporting to the Director Regulatory Affairs, Mass Markets South, this role serves as a key regulatory resource to internal stakeholders by monitoring regulatory and legislative developments, evaluating business impacts, and helping ensure regulatory requirements are effectively implemented across the organization. Evaluate wholesale market rule changes and summarize impacts related to settlements, resource adequacy, reliability initiatives, ancillary services, cost allocation, and market operations.
Regulatory Affairs Manager Electrolit USARegulatory Affairs ManagerHouston, TexasThis role maintains strong alignment with the Electrolit Global Regulatory Team to ensure consistency and best practices across markets and collaborates closely with internal and external legal counsel to address regulatory and legal matters. Operating cross-functionally across departments, the Regulatory Affairs Manager manages regulatory documentation, labeling compliance, advertising and serves as the primary liaison with regulatory authorities.
Permitting & Regulatory Affairs Manager (Remote) BaRupOn LLCPermitting & Regulatory Affairs Manager (Remote)Liberty, TXRemoteBaRupOn LLC is a multi-sector infrastructure and energy company with a bold mission: to deliver transformational projects that power communities, advance healthcare, and drive sustainable development across the globe. With operations spanning solar and gas-powered energy systems, complex civil construction, and medical and healthcare innovation, BaRupOn operates at the intersection of resilience, scale, and impact.
Regulatory Affairs Manager Karwell TechnologiesRegulatory Affairs ManagerDallas, TXMust be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts on complex projects. Demonstrated hands-on experience in preparing regulatory clearance/approvals for IVD products in the EU, USA, OUS; (Preferred experience: working experience with IVD submissions under IVDR Regulations is highly desirable).
Regulatory Affairs Manager Katalyst Healthcares & Life SciencesRegulatory Affairs ManagerDallas, TXMust be able to work effectively in a strongly matrixed team-oriented structure using excellent communication, interpersonal and relationship management skills to successfully interact with Clinical, Research and Development, Manufacturing, Quality, Marketing, Operations and corporate partner counterparts on complex projects. Demonstrated hands-on experience in preparing regulatory clearance/approvals for IVD products in the EU, USA, OUS; (Preferred experience: working experience with IVD submissions under IVDR Regulations is highly desirable).
Senior Regulatory Affairs Manager Medtronic PlcSenior Regulatory Affairs ManagerFort Worth, TXThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Sr. Regulatory Affairs Manager Karwell TechnologiesSr. Regulatory Affairs ManagerDallas, TXAssists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to QOL initiatives. Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.
Sr. Regulatory Affairs Manager Katalyst Healthcares & Life SciencesSr. Regulatory Affairs ManagerDallas, TXAssists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to QOL initiatives. Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.
NewDialysis Facility Administrator U.S. Renal CareDialysis Facility AdministratorCollege Station, TXContinuously monitor to ensure that a safe and sanitary physical environment is maintained throughout the facility; that all equipment is maintained and functions properly; and that adequate and appropriate inventory levels of all supplies are available and used correctly. STAFF DEVELOPMENT/ RETENTION Ensure all staff meet required qualifications for position held and perform duties within limitations established by and in accordance with company policy/procedures, health care professionals practice acts, applicable state and federal laws and regulations.
Regulatory Affairs & Project Manager QontoRegulatory Affairs & Project ManagerParis, TXToday, his scope spans France and Qonto's international markets and covers product governance, supervisory interactions and licensing, internal governance and committees, data protection and ethics, as well as regulatory reporting. Strengthen supervisory relationships: Act as a key point of contact for the ACPR and Qonto's branch supervisors, building constructive relationships and ensuring clear, reliable and timely communication.
Manager, Regulatory Affairs Strategy Alcon IncManager, Regulatory Affairs StrategyFort Worth, TXThis individual will play a critical role in driving regulatory excellence, supporting business objectives, and enabling timely, compliant access to innovative products across global markets while upholding Alcon's commitment to quality, compliance, and patient safety. The Manager, Regulatory Affairs Strategy (Professional Path) is responsible for leading regulatory strategy, compliance, and lifecycle management activities for Alcon's Dry Eye Ocular Health and Contact Lens Care portfolio.
NewRegulatory Affairs Compliance Manager PBF EnergyRegulatory Affairs Compliance ManagerThe Woodlands, TexasThis role includes day-to-day management of ISCC program requirements and risk management, continuous monitoring of regulatory and system updates, and direct accountability for mass balance, conversion factors, GHG calculations, and audit readiness and execution. Factors such as scope and responsibilities of the position, candidate’s work experience, education/training, job-related skills and internal peer equity will be considered in determining the selected candidate’s compensation.
NewRegulatory Affairs Compliance Manager PBF Energy IncRegulatory Affairs Compliance ManagerThe Woodlands, TX$106,787.51–$189,503.19 / yearThis role includes day-to-day management of ISCC program requirements and risk management, continuous monitoring of regulatory and system updates, and direct accountability for mass balance, conversion factors, GHG calculations, and audit readiness and execution. Factors such as scope and responsibilities of the position, candidate's work experience, education/training, job-related skills and internal peer equity will be considered in determining the selected candidate's compensation.
["Senior Regulatory Affairs Project Manager I, MILCON","Senior Regulatory Affairs Project Manager I, MILCON"] Icon["Senior Regulatory Affairs Project Manager I, MILCON","Senior Regulatory Affairs Project Manager I, MILCON"]AustinAssist Program Manager in developing and influencing federal building codes, UFCs, and government policies that align with ICON's technology capabilities and promote 3D-printed construction adoption across the public sector participate in federal technical committees and working groups related to innovative construction methods. Collaborate with internal technical teams-including testing, materials science, product engineering, and operations-to integrate federal regulatory requirements into product development; ensure validation efforts support approval pathways and resolve technical challenges that impact government acceptance.
Manager - Quality & Regulatory Affairs EnvistaManager - Quality & Regulatory AffairsLubbock, TXEnvista will consider unsolicited referrals and/or resumes submitted by vendors such as search firms, staffing agencies, professional recruiters, fee-based referral services and recruiting agencies (Agency) to have been referred by the Agency free of charge and Envista will not pay a fee for any placement resulting from the receipt such unsolicited resumes. An Agency must obtain advance written approval from Envista's internal Talent Acquisition or Human Resources team to submit resumes, and then only in conjunction with a valid fully-executed contract approved by the Global Talent Acquisition leader and in response to a specific job opening.
["Senior Manager, CMC Global Regulatory Affairs","Senior Manager, CMC Global Regulatory Affairs"] Otsuka America Pharmaceutical["Senior Manager, CMC Global Regulatory Affairs","Senior Manager, CMC Global Regulatory Affairs"]AustinThe Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global regulatory strategies for CMC aspects of small molecule and biological/biotechnological products during late-stage development and throughout the commercial lifecycle. Develop and maintain collaborative relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs, Global Regulatory Strategy, Manufacturing facilities, Global Quality, Technical Operations, Business Development etc.] as well as affiliates, external partner companies, contract manufacturers, packagers and suppliers etc.
Manager, Regulatory Affairs And Compliance Nordson CorporationManager, Regulatory Affairs And ComplianceAllen, TXPrepares regulatory strategies and maintains submissions for U.S. and International markets, including but not limited to 510(k)s and Technical Files, to ensure timely approval of devices and continued regulatory support of marketed devices. A highly participative leader, responsible for the hands-on management and direction of regulatory and document control personnel and for implementing best practices, continuous improvement, and corrective/preventive actions as necessary.
Manager, Regulatory Affairs and Compliance NordsonManager, Regulatory Affairs and ComplianceTexasPrepares regulatory strategies and maintains submissions for U.S. and International markets, including but not limited to 510(k)s and Technical Files, to ensure timely approval of devices and continued regulatory support of marketed devices. A highly participative leader, responsible for the hands-on management and direction of regulatory and document control personnel and for implementing best practices, continuous improvement, and corrective/preventive actions as necessary.
Manager, Regulatory Affairs Strategy Alcon ResearchManager, Regulatory Affairs StrategyFort Worth, TexasThis individual will play a critical role in driving regulatory excellence, supporting business objectives, and enabling timely, compliant access to innovative products across global markets while upholding Alcon’s commitment to quality, compliance, and patient safety. The Manager, Regulatory Affairs Strategy (Professional Path) is responsible for leading regulatory strategy, compliance, and lifecycle management activities for Alcon’s Dry Eye Ocular Health and Contact Lens Care portfolio.
Manager, Regulatory and Market Affairs Pattern Energy Group IncManager, Regulatory and Market AffairsHouston, TX$103,000–$138,000 / yearA key function of this role will be to identify, research, analyze, and synthesize the cross section of regulatory and wholesale market rules impacting Pattern's existing and planned assets in WECC, MISO, ERCOT, SPP, PJM and other priority markets as needed. Importantly, the role will support the coordination with expert consultants and internal SMEs to clearly and regularly identify and lead Pattern's engagement in regulatory and market design changes, develop Pattern's positions and execute on strategies to achieve desired objectives.
Regulatory Affairs Manager - Diabetes Care (on-site) Abbott LaboratoriesRegulatory Affairs Manager - Diabetes Care (on-site)Austin, TX$114,000–$228,000 / yearAs a member of the U.S. Regulatory Affairs management team, the successful candidate will lead and develop talent, shape regulatory strategy, and partner across functions to bring innovative products to market, whilst driving regulatory excellence for the manufacture, change management, and ongoing supply of the Libre portfolio. Drive and provide strategic guidance on FDA pathways, submissions, and interactions, including pre-submissions, 510(k), PMA, and post-market activities.
Manager, Regulatory Affairs - Clinical Research Baylor College of MedicineManager, Regulatory Affairs - Clinical ResearchHouston, TX$111,118–$130,000 / yearDirectly supervises Regulatory Affairs Associates and Senior Associates, including assigning and prioritizing workload, monitoring performance, and ensuring equitable distribution of study portfolios. Provides regulatory support for clinical protocols by coordinating submissions, reviewing regulatory content for completeness and compliance, and ensuring alignment with institutional requirements.
Director / Manager Tariffs and Regulatory Affairs Kinder Morgan IncDirector / Manager Tariffs and Regulatory AffairsHOUSTON, TXPrimary Purpose: To work with all Kinder Morgan products pipeline regulated assets (Calnev, Double Eagle, Hiland Crude (gathering), KM Crude and Condensate (KMCC), Products (SE) Pipe Line (PPL), Central Florida Pipeline (CFPL), and SFPP) plus Wink (CO2 group) in matters regarding Federal Energy Regulatory Commission (FERC) and state liquids pipeline regulations, in order to create and maintain tariff documents, set rates, adjust and defend rates (including the collection and organizing of pipeline volume and rate base data), and create and maintain tariff rules. Teamwork/Cooperation: Works effectively with team/work group, as well as with other departments and/or outside contractors/agencies to accomplish organizational goals; takes action that respect the needs and contributions of others; takes responsibility for actively participating and contributing to team efforts; supports a team consensus or decision; acts as team facilitator when appropriate, promotes team concepts.
Analyst, Regulatory Affairs Oscar Health InsuranceAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Analyst, Regulatory Affairs Oscar HealthAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Analyst, Regulatory Affairs Oscar Health IncAnalyst, Regulatory AffairsDallas, TXRemote$28.30–$37.15 / hourYou will support the Regulatory Affairs Evidence of Coverage team by serving as a resource on Oscar processes and identify risks to escalate in partnership with their manager. Responsibilities: Support annual QHP filings by ensuring the quality and timeliness of annual filing inputs through initial submission and regulator facing negotiation periods.
Director Regulatory Affairs Houston Methodist HospitalDirector Regulatory AffairsHouston, TXProvides comprehensive management oversight and regulatory guidance to move projects forward from basic laboratory research to regulated environments: Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), First in Human (FIH), early phase clinical trials. Houston Methodist Research Institute supports research programs and infrastructure that enable faculty across the system to bring new scientific discoveries to patients as rapidly as possible through the full cycle of a cure from conceptual bench research, to prototyping and development, to clinical trials and FDA approval.
Senior Regulatory Affairs Specialist EnovisSenior Regulatory Affairs SpecialistUSA, TXWorking as part of a global RA function, the role will also support in sustainable regulatory activities such as management of postmarket surveillance activities on behalf of legal manufacturers, completing regulatory impact assessments for product changes and providing other regulatory SME support to the business as needed. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.
Senior Regulatory Affairs Specialist Enovis CorpSenior Regulatory Affairs SpecialistAustin, TXWorking as part of a global RA function, the role will also support in sustainable regulatory activities such as management of postmarket surveillance activities on behalf of legal manufacturers, completing regulatory impact assessments for product changes and providing other regulatory SME support to the business as needed. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.
Associate Regulatory Affairs Specialist - Onsite MedtronicAssociate Regulatory Affairs Specialist - OnsiteFort Worth, TexasThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. (“Medtronic”) in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Associate Regulatory Affairs Specialist - Onsite Medtronic PlcAssociate Regulatory Affairs Specialist - OnsiteFort Worth, TXThe following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). If you are applying to perform work for Medtronic, Inc. ("Medtronic") in any position which will involve performing at least two (2) hours of work on average each week within the unincorporated areas of Los Angeles County, you can find here a list of all material job duties of the specific job position which Medtronic reasonably believes that criminal history may have a direct, adverse and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.
Associate Director, Regulatory Affairs Tonix PharmaceuticalsAssociate Director, Regulatory AffairsFort Worth, Maryland$136,500–$200,000 / yearTonix is also advancing a pipeline of immunology programs, including TNX-4800, a Phase 2 ready long-acting human anti- Borrelia OspA monoclonal antibody (mAb) for the prevention of Lyme disease in the U.S., and TNX-1500, a Phase 2 ready third-generation CD40 ligand inhibitor for the prevention of kidney transplant rejection. The Associate Director, Regulatory Affairs can work autonomously and will support all aspects of this process including early phase interactions with regulatory authorities (FDA and/or global), providing direction and actively participating in overall preparation of activities with cross-functional teams to advance the drug development program.
Director, Molecular Regulatory Affairs North America DiaSorin SpADirector, Molecular Regulatory Affairs North AmericaAustin, TXAs we continue to expand our presence in North America, we are seeking a Director of Molecular Regulatory Affairs, North America to support the Molecular RA team and RA VP NA in identified the regulatory strategy, ensuring our products meet all regulatory requirements in the region while supporting our ambitious growth in the Immuno and Molecular Diagnostics markets. Key Responsibilities: Cross Functional cooperation on Key projects: Support RA team in developing and implementing regulatory strategies for the Molecular Diagnostics portfolio in North America, ensuring timely market access for all new products and continued compliance for existing products.
NewMedical Affairs & Scientific Engagement Manager ARTIDISMedical Affairs & Scientific Engagement ManagerHouston, TXYou will develop and maintain strong relationships with clinicians, researchers, healthcare institutions, and key opinion leaders while leading scientific engagement activities, supporting evidence generation, and representing ARTIDIS at major medical and scientific conferences. Working closely with the Houston team and Basel headquarters, you will serve as a bridge between ARTIDIS' Scientific, Clinical, Commercial, and Marketing teams, translating our innovative cancer diagnostics technology into meaningful clinical conversations.
NewMedical Affairs & Scientific Engagement Manager (Remote) ARTIDISMedical Affairs & Scientific Engagement Manager (Remote)Houston, TXRemoteYou will develop and maintain strong relationships with clinicians, researchers, healthcare institutions, and key opinion leaders while leading scientific engagement activities, supporting evidence generation, and representing ARTIDIS at major medical and scientific conferences. Working closely with the Houston team and Basel headquarters, you will serve as a bridge between ARTIDIS' Scientific, Clinical, Commercial, and Marketing teams, translating our innovative cancer diagnostics technology into meaningful clinical conversations.
Public Affairs Manager, Regional Data Centers Google LLCPublic Affairs Manager, Regional Data CentersTXGoogle is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting. Build and maintain critical relationships with government officials, community leaders, and key opinion formers to ensure a positive and sustainable operating environment for our facilities.
Senior Regulatory Affairs Analyst Keurig Dr Pepper IncSenior Regulatory Affairs AnalystFrisco, TX$76,400–$115,000 / yearThe analyst also monitors and interprets relevant government and technical information impacting our brands, develops finished-product regulatory specifications, and provides regulatory guidance to business partners and cross-functional project teams. By enabling compliant, science-based claims, labeling, and advertising, the function protects consumers and the business while supporting KDPs competitive edge.
Sr. Manager, Corporate Affairs (Central) Digital Realty Trust IncSr. Manager, Corporate Affairs (Central)Dallas, TXPlatformDIGITAL, the company's global data center platform, provides customers with a secure data meeting place and a proven Pervasive Datacenter Architecture (PDx) solution methodology for powering innovation and efficiently managing Data Gravity challenges. Working closely with Government Affairs, business leaders, media, and community stakeholders, you''ll help shape our public narrative, support strategic initiatives, manage reputational risks, and ensure consistent messaging across the region.
Environmental Affairs Manager RepsolEnvironmental Affairs ManagerHouston, TXJob Summary: Repsol Renewables North America is seeking an environmental professional to provide development support and management of environmental and regulatory permitting for large-scale renewable generation and storage projects across the U.S. This position reports to and works closely with the Director of Environmental Affairs and Permitting. Direct experience with National Environmental Policy Act (NEPA) compliance reviews, state-level environmental quality act reviews and state-level energy regulatory proceedings, local zoning authorizations, as well as post-permitting compliance and implementation.
Manager Government Affairs And Public Outreach Boardwalk Pipeline PartnersManager Government Affairs And Public OutreachHouston, TXStrong leadership and communication skills, collaboration on policy development with the ability to work with key external government stakeholders on energy issuesStrong understanding of energy and environmental policy issuesFamiliarity with federal and state legislative and regulatory processesOutstanding written and verbal communicationsSelf-starter with the ability to operate with a high degree of autonomy applying effective prioritization, analytical problem solving and planning skillsProven track record of building relationships with a diverse range of collaboratorsAbility to travel frequently. Support affected landowner reviews with the internal land team and work with outside PR Firms to identify key landowners and stakeholders for our asset base Coordinate required outreach prior to initial landowner contacts and survey permission and ensure consistent messaging across all Boardwalk Pipelines' Project-level communications.
Manager Government Affairs and Public Outreach Boardwalk Pipeline Partners LPManager Government Affairs and Public OutreachHouston, TXSupport affected landowner reviews with the internal land team and work with outside PR Firms to identify key landowners and stakeholders for our asset base Coordinate required outreach prior to initial landowner contacts and survey permission and ensure consistent messaging across all Boardwalk Pipelines' Project-level communications. Monitor, analyze, and report to Senior Management on legislative and regulatory developments that impact ongoing operations and interstate pipeline Projects development including pipeline permitting, environmental compliance, infrastructure development, and energy policy.
Senior Manager, Medical Affairs Operations - Remote Agios PharmaceuticalsSenior Manager, Medical Affairs Operations - RemoteHouston, TXRemote$131,035–$196,553 / yearManage the execution of Agios’ patient advocacy conference plans for PK deficiency, thalassemia, and sickle cell disease; participate in cross-functional planning meetings; obtain compliance approval for related materials; and attend virtual and in-person conferences, when needed. Provide operational and project management support to the US patient advocacy team, ensuring smooth day-to-day coordination across priorities, stakeholders, and deliverables, and flex to support various other functions within Medical Affairs as needs arise.
Government Affairs & Strategic Partnerships Jr. Manager Flix SEGovernment Affairs & Strategic Partnerships Jr. ManagerDallas, TXYou will develop strategic partnerships with public and private entities, navigate complex government processes, and ensure compliance while establishing access to high-value transportation hubs across the country. Manager, you will support market expansion by securing access to critical infrastructure, managing relationships with key stakeholders, and driving operational success in a highly regulated environment.
Environmental Affairs Manager Repsol SAEnvironmental Affairs ManagerHouston, TXJob Summary: Repsol Renewables North America is seeking an environmental professional to provide development support and management of environmental and regulatory permitting for large-scale renewable generation and storage projects across the U.S. This position reports to and works closely with the Director of Environmental Affairs and Permitting. Direct experience with National Environmental Policy Act (NEPA) compliance reviews, state-level environmental quality act reviews and state-level energy regulatory proceedings, local zoning authorizations, as well as post-permitting compliance and implementation.
Manager, Government Affairs Pattern Energy Group IncManager, Government AffairsHouston, TX$103,000–$138,000 / yearIntegrates input from development, operations, and commercial teams, as well as executive leadership, to identify policy-driven risks and opportunities, and to articulate the company''s positions on key issues; leads internal teams in prioritizing and analyzing the impact of critical legislative and regulatory issues based on the company's business plan; reports on key issues and impacts to relevant internal staff and executive management team. Additionally, the role will need to manage multiple initiatives at once and work closely with the development and other departments to design and execute comprehensive external affairs strategies to achieve desired policy outcomes to support the company's commericial objectives.
Government Affairs & Strategic Partnerships Jr. Manager FlixGovernment Affairs & Strategic Partnerships Jr. ManagerDallas, TX$70,000–$80,000 / yearYou will develop strategic partnerships with public and private entities, navigate complex government processes, and ensure compliance while establishing access to high-value transportation hubs across the country. Manager , you will support market expansion by securing access to critical infrastructure, managing relationships with key stakeholders, and driving operational success in a highly regulated environment.