Oncology Account Executive/ Solid Tumors (, PR, United States)

Company Description About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube. Job Description Ejecutar estrategias y tácticas de marca en el campo, rendimiento de ventas (sales performance), administrar eficazmente el territorio asignado y las cuentas específicas, establecer relaciones sólidas con los clientes y capacidad de resolución de necesidades del cliente para maximizar el rendimiento de ventas (sales performance) a corto y largo plazo, colocando al paciente en el centro de cualquier esfuerzo y operando dentro código de conducta de AbbVie, políticas y todas las leyes y regulaciones aplicables. Implementación de la estrategia de la marca para poder asegurar el posicionamiento planteado por el equipo de marketing. Cumplimiento y alineación de los indicadores de ejecución (KPIs) como frecuencia en la visita, cobertura de visita diaria establecida por la unidad de negocio, mantenimiento y actualización de fichero médico de acuerdo con la estrategia. Manejar objeciones, malentendidos e inquietudes de manera eficaz y obtener constantemente llamadas a la acción lógicas y razonables para cerrar cada llamada de ventas. Aspirar a satisfacer las necesidades, retos y expectativas de los clientes de manera proactiva y continua, con el fin de construir relaciones confiables con los clientes y lograr acuerdos de beneficio mutuo entre AbbVie y los clientes. Desarrollar continuamente un entendimiento sobre las necesidades y expectativas del cliente, el panorama del mercado de sus territorios, los competidores, los segmentos de mercado / dinámica de cuentas, enfermedades, productos, experiencia clínica y de ventas y compartir esta información de inteligencia de mercado con el resto del Infield Team, el Brand Team y Gerentes de ventas, para lograr alineación anticipar cambios y desafíos en el entorno y optimizar la estrategia de marca y su ejecución. Diferenciar la propuesta de valor de AbbVie con los proveedores de salud asignados e identificar, desarrollar y mantener a los expertos y “speakers/ advocates” para maximizar el desempeño de la marca. Qualifications Licenciatura en Administración o equivalente. Experiencia en la industria farmacéutica en áreas comerciales como: ventas alta especialidad, capacitación, asociado de marca, prácticas profesionales en ventas. Preferentemente con un historial comprobado de éxito en el desempeño de las ventas dentro de las áreas terapéuticas respectivas. Más de 6 años de experiencia como representante de ventas, deseable en alta especialidad Historial comprobado de éxito en ventas y sólidas habilidades de presentación. Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html J-18808-Ljbffr

Maternal-Fetal Medicine Chief Director (New Brunswick)

Maternal-Fetal Medicine Chief Director The Department of Obstetrics, Gynecology, and Reproductive Sciences at Rutgers Robert Wood Johnson Medical School, in partnership with RWJBarnabas Health, is seeking a highly qualified and collaborative physician to serve as the Chief of the Maternal-Fetal Medicine Division. This full-time, open-rank position offers the opportunity to lead and further develop a growing academic division dedicated to exceptional high-risk pregnancy care, education, and research. The Chief will report to the Chair of Obstetrics, Gynecology, and Reproductive Sciences and work closely with Women’s Health service line leadership to advance maternal and fetal care throughout the region. The department welcomes accomplished senior or mid-career faculty members and thought leaders prepared to take the next step in their careers. Leadership development and support will be available for candidates who demonstrate strong potential but have not previously held a Chief or senior leadership title. Position Highlights Provide strategic leadership for the clinical, educational, research, and administrative activities of the MFM Chief Help shape the continued growth of maternal-fetal medicine and regional perinatal services across Rutgers Health and RWJBarnabas Health Mentor and support a talented team of early-career faculty, fellows, residents, and medical students Maintain an active clinical practice across inpatient and outpatient maternal-fetal medicine services Expand high-risk pregnancy care, prenatal diagnosis, fetal therapy, outreach, and telemedicine programs Direct and strengthen the accredited MFM fellowship program while maintaining compliance with ACGME standards Collaborate with general obstetricians, neonatologists, pediatric medical and surgical specialists, pediatric cardiologists, nurses, and other multidisciplinary partners Advance clinical quality, patient experience, program outcomes, productivity, and financial performance Promote clinical, translational, and basic science research while supporting publications, national presentations, and external funding Recruit, develop, mentor, and retain exceptional faculty and staff Support the department’s commitment to complex family planning and comprehensive reproductive healthcare The division offers a highly collaborative academic environment with access to advanced clinical programs and multidisciplinary expertise. The successful candidate will have the opportunity to build upon the program’s existing strengths while developing new services, expanding its academic presence, and shaping its long-term direction. Candidate Requirements MD, DO, or equivalent medical degree Board certification in Obstetrics and Gynecology Board certification in Maternal-Fetal Medicine through the American Board of Obstetrics and Gynecology Eligible for medical licensure in New Jersey Minimum of five years of clinical experience in maternal-fetal medicine Expertise in obstetric ultrasound and invasive MFM procedures Demonstrated record of clinical excellence, academic achievement, and commitment to medical education Clinical research experience and an established record of scholarly activity Experience with program development, faculty mentorship, and multidisciplinary collaboration Evidence of a national presence through publications, invited presentations, or other professional contributions Previous formal leadership experience is desired, although not required. Candidates with experience securing extramural research funding, leading multidisciplinary teams, and advancing quality improvement or population health initiatives in perinatal care are strongly encouraged to apply. Compensation The position offers a minimum salary of $550,448 , along with a comprehensive benefits package. Final compensation will be based on qualifications, experience, expertise, market benchmarks, available funding, and internal equity. Benefits may include medical, prescription, and dental coverage; paid vacation and holidays; retirement plans; educational benefits; life insurance; and employee discount programs. J-18808-Ljbffr

Senior Principal Software Engineer - CRDN (Northern)

We anticipate the application window for this opening will close on - 10 Sep 2026 En Medtronic, puedes empezar una carrera para toda la vida que se centre en la investigación y en la innovación y que defienda la equidad y el acceso a la atención sanitaria para todos. Tu liderazgo dejará huella, eliminando obstáculos para impulsar la innovación en un mundo más conectado y humanitario. Un día normal Senior Principal Software Engineer Careers that Change Lives Medtronic is a global leader in medical technology, services, and solutions that take on the healthcare industry's greatest challenges. Engineers and Scientists create our market-leading portfolio of innovations. Join the Coronary & Renal Denervation team and help us bring the next generation of life-changing medical technology to patients worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. Come for a job, stay for a career. Treatments We Offer: Renal Denervation Key Technologies Symplicity Spyral™ Renal Denervation (RDN) System Medtronic’s Coronary and Renal Denervation (CRDN) business is looking for a Senior Principal Software Engineer to be part of a high‑performing team that is revolutionizing the design and development of energy based therapeutic medical devices to treat hypertension. In this role, you will leverage both your technical breadth and business acumen to support the next generation medical device software products. This position is in Mounds View, MN. within the Coronary and Renal Denervation (CRDN) unit. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In‑person exchanges are invaluable to our work. We are working on‑site 4 days per week as part of our commitment to fostering a culture of professional growth and cross‑functional collaboration as we work together to engineer the extraordinary. This role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects. We believe that when people from different cultures, genders, and points of view come together, innovation is the result —and everyone wins. Medtronic walks the walk, creating an inclusive culture where you can thrive. Senior Principal Software Engineer The Senior Principal Software Engineer will serve as the technical leader and be responsible for architecting, designing, building, and scaling embedded software for next generation medical device. This role combines deep hands‑on engineering expertise with architectural leadership, technical decision‑making, and mentorship. The Senior Principal Engineer drives technical strategy, ensures engineering excellence, and partners closely with cross‑functional teams and business stakeholders to deliver impactful solutions. Responsibilities Architect, Design, develop, test, and maintain high‑quality medical device embedded software solutions as part of the software team in accordance with Agile principles and Scrum methodologies Define and uphold architectural standards, design patterns, and best practices Make high‑impact technical decisions that align with long‑term platform and business strategy Review and guide system designs, APIs, data models, and integration approaches Optimize system performance, reliability, and scalability Ensure solutions meet security, privacy, and compliance requirements Lead Risk Assessment activities and Requirements development. Cross‑functional team collaboration with HW and Systems partners, including integration team, testing team, Quality, System V&V…etc. Drive continuous improvement through retrospectives and lessons learned Provide leadership in solving engineering problems and fostering creativity and innovation in design and problem solutions Follow Medical device regulations (IEC 62304, IEC 82304, FDA…etc.) Stay up‑to‑date with industry trends and best practices in software development, and make recommendations for process improvements Qualifications Bachelor’s degree in computer engineering, electrical engineering, computer science, engineering, or a related technical discipline and minimum of 10 years of work experience OR advanced degree in computer engineering, electrical engineering, computer science, engineering, or a related technical discipline with 8 years of work experience. Nice to Have Knowledge of microservices architecture and event‑driven systems Familiarity with FPGA Experience in regulated or enterprise‑scale environments Knowledge of cloud and connected medical devices Excellent collaboration skills across engineering, quality, and regulatory teams Pragmatic decision‑making that balances compliance, security, and delivery velocity Clear communication with both technical and non‑technical stakeholders Location This position is in Mounds View, MN. within the Coronary and Renal Denervation (CRDN) unit. Working Hours/Travel This role will require less than 10% of travel to enhance collaboration and ensure successful completion of projects. Benefits and Compensation Beneficios y compensación Medtronic ofrece un salario competitivo y un paquete de beneficios flexible El compromiso con las vidas de nuestros empleados es el centro de nuestros valores. Reconocemos sus aportes. Comparten el éxito que contribuyen a crear. Ofrecemos una amplia gama de beneficios, recursos y planes de compensación competitivos diseñados para apoyarlo en cada etapa de su carrera profesional y de la vida. Salary ranges for U.S (excl. PR) locations (USD):$178,400.00 - $267,600.00 This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP). The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others). 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). Incentive plans, 401(k) plan plus employer contribution and match, Short‑term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non‑qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums). Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Equal Opportunity Statement Es la política de Medtronic proporcionar igualdad de oportunidades de empleo (EEO, por sus siglas en inglés) para todas las personas, independientemente de su edad, color, origen nacional, estado de ciudadanía, discapacidad física o mental, raza, religión, credo, género, sexo, orientación sexual, identidad y/o expresión de género, información genética, estado civil, estado en relación a la asistencia pública, estado como veterano o cualquier otra característica protegida por las leyes federales, estatales o locales. Además, Medtronic proporcionará asistencia especial razonable para los individuos calificados con alguna discapacidad. Additional Employment Requirements En Medtronic, tenemos el compromiso de fomentar un entorno donde los empleados puedan prosperar y tener un impacto significativo. En consonancia con nuestro enfoque de planificación de la fuerza laboral en toda la empresa, el patrocinio de autorización de trabajo de los EE. UU. (H‑1B, TN, J, etc.) se ofrece exclusivamente para roles de nivel principal y superior, donde la experiencia especializada se alinea con las necesidades comerciales a largo plazo. Los roles por debajo del nivel principal requieren que los candidatos posean una autorización de trabajo sin restricciones de los EE. UU. al momento de la contratación y durante la duración del empleo. Para los representantes de ventas y otros empleados de campo orientados al paciente, ir a un entorno de… Este empleador participa en el programa federal E‑Verify para confirmar la identidad y la autorización de empleo de todos los empleados recién contratados. Para obtener más información sobre el programa E‑Verify, haga clic aquí (https://www.e-verify.gov/employees). Para obtener información actualizada sobre las solicitudes de empleo, vaya a la página de inicio de sesión para candidatos e inicie sesión para verificar el estado de su solicitud. Si necesita ayuda para completar la solicitud, envíe un correo electrónico a [email protected]. Para solicitar la eliminación de su información personal de nuestros sistemas, envíe un correo electrónico a [email protected]. J-18808-Ljbffr

Assistant General Counsel, AI, Emerging Technologies, & Strategic Agreements (Santa Monica)

Job Type: Regular Assistant General Counsel,AI,Emerging Technologies,& Strategic Agreements The RAND Corporation’s Office of the General Counsel (OGC) is seeking a highly motivated, professional attorney to join our Legal Strategy & Advancement Team as the Assistant General Counsel focusing on AI,Emerging Technologies & Strategic Agreements . OpportunitySummary Reports directly to the Vice President, General Counsel, and Corporate Secretary. Your core responsibilities would include: technology transactions involving AI and other emerging technologies; drafting and negotiating commercial contracts, IP agreements, and licensing arrangements; helping develop new ways of leveraging RAND’s IP; and addressing novel challenges as they arise. We are seeking an attorney with: Practical experience using AI tools to provide timely, accurate legal advice, with a continuous improvement mindset and enthusiasm for exploring new AI capabilities; A focus on helping clients identify risks and opportunities, and on finding innovative solutions to problems; Comfort with wearing \multiple hats\ and in building legal infrastructure from the ground-up; and Passion for the legal subjects on which the attorney advises. About RAND OGC We are a high-performing team of talented legal professionals that support the entire enterprise – everything we do is for the purpose of enabling RAND to deliver on its mission. While each of our team members has specialist skills, we are also intellectually curious generalists who engage across the full range of issues and opportunities experienced by RAND. Even as RAND researchers leverage and evaluate the most advanced frontier AI models and capabilities in tackling the world’s most complex public policy challenges, our team has fully adopted leading edge AI legal tools to enhance and advance our legal services – with continuous exploration of new capabilities and a willingness to challenge long standing assumptions and practices. We combine this with high levels of engagement across the organization and collaboration within the team and with the people we support, enabling us to confidently provide thoughtful, practical, and actionable advice at the speed of a fast-moving organization. RAND OGC has three levels of attorney positions: Counsel, Assistant General Counsel, and Associate General Counsel, reflecting progressively increasing levels of established skill, experience, and responsibility. The Role As part of an OGC team focused on advancing RAND’s mission through innovative solutions, the primary responsibilities of this role will include: Advising on technology transactions and emerging technology matters, including artificial intelligence, digital assets, data use, and related legal issues affecting RAND’s research and operations; Drafting, negotiating, and managing a wide range of commercial agreements, including licensing agreements, NDAs, vendor agreements, technology agreements, and similar transactions; Advising on intellectual property matters, including IP strategy, protection of RAND’s IP assets, patents, and negotiation of IP-related provisions in research and commercial agreements; Advocacy with research sponsors on behalf of RAND in conjunction with research division leadership, including periodic in-person visits to sponsor locations; Collaborating with the Director of Contracts and other RAND operations personnel to establish and update high-quality, agile processes for the review and negotiation of contracts and agreements; Proactively identifying risks and working with stakeholders to design and implement solutions; Tasking and directing outside counsel as required; Advising staff on compliance with applicable laws and regulations; and Special projects assigned by the General Counsel. Other responsibilities may include: Advising RAND’s Development function with respect to the terms of charitable gifts and grants; Advising and training on export control and trade compliance matters, including ITAR, EAR, and related regulatory frameworks applicable to RAND’s domestic and international activities, including AUKUS; and Advising on federal government contracting matters, including FAR/DFARS compliance and related procurement issues. RAND’s OGC roles tend to involve a unique combination of responsibilities–in our experience no candidate (even the ones we hire!) ever checks every single box. If you’re excited about this role, think you have what it takes, and are ready to learn, we encourage you to apply. Qualifications The requirements for this Assistant General Counsel role are as follows: Required: At least six (6) years of experience as a practicing attorney with some combination of substantive experience in technology transactions, intellectual property, commercial agreements, or related transactional areas; Detail-oriented, works well under pressure, and has an affinity for RAND’s Mission; Proven problem-solver who takes ownership of assigned areas of responsibility; Demonstrated ability to confidently provide sound judgment even in ambiguous situations; Collaborative, collegial, and skilled at building consensus with diverse professional groups; Demonstrated desire to take on increasing levels of responsibility and confidence to engage in novel legal issues that may be outside prior experience; Ability to identify priories and adjust as necessary to meet unanticipated needs; and Ability to travel occasionally to other RAND offices (primarily in the U.S.). Preferred/ \Plus\ Factors: Experience working in-house for a technology company, research institution, or organization engaged in emerging technology work; Experience working for (or with) a non-profit organization; and/or Substantive experience pertaining to any of the following: federal government contracting, FAR/DFARS compliance, or government procurement matters; export control regulations (EAR, ITAR) or trade compliance programs; cybersecurity; any of the \other responsibilities\ described above Education & Licensing J.D. and licensed to practice law (in good standing). If not licensed to practice law in the state of employment, must qualify under the Supreme Court of Virginia’s Rule 1A:5 or the requirements for Registered In-House Counsel for the State of California (as applicable). Licensure in California, Virginia, Pennsylvania, D.C., or New York is a plus. Security Clearance This position requires the ability to obtain and maintain a U.S. Government Security Clearance and DHS Fitness. Accordingly, U.S. citizenship is required. Location This role is based in either RAND’s Arlington, VA (Washington DC area) office or Santa Monica, CA (Los Angeles area) headquarters and is eligible for RAND’s hybrid work environment. Candidates should expect to work from a RAND office about three days per week on average. Salary Range $177,500 - $235,000 RAND considers a variety of factors when formulating an offer, including but not limited to, the specific role and associated responsibilities; a candidate’s work experience, education/training, skills, expertise; and internal equity. The salary range includes base pay plus RAND’s sabbatic pay (which provides additional compensation above base pay when vacation is taken). In addition, RAND provides strong benefits including health insurance coverage, life and disability insurance, savings plan, paid time-off and more. Equal Opportunity Employer J-18808-Ljbffr

Vice President, Global Technical Services – Manufacturing Sciences and Engineering (Indianapolis)

Define and lead the global TSMS and Engineering strategy supporting manufacturing platforms Establish frameworks for process lifecycle management and technical standards Oversee technology transfer and process validation from development to commercial manufacturing Ensure regulatory compliance and technical readiness across internal and external sites Lead global technical support, investigations, and continuous improvement programs Drive process robustness, yield, and operational excellence Provide strategic leadership for global facilities and automation Manage the capital project portfolio Ensure GMP and safety compliance for equipment and utilities Develop and deliver a roadmap for next-generation manufacturing capabilities Implement AI, robotics, and advanced digital technologies Requirements BSc, MSc, or PhD in Chemical Engineering, Mechanical/Industrial Engineering, Biotechnology, Pharmaceutical Sciences, or a related technical field Minimum of 15 years of experience in pharmaceutical, biologics, or animal health manufacturing Substantial leadership experience in technical services, TSMS, or engineering Deep expertise in process development and validation Strong strategic leadership skills Experience managing multi-site technical organizations Additional business or leadership education, such as an MBA or comparable executive program (preferred) Proven track record of introducing advanced manufacturing technologies and digital/automation solutions in a regulated GMP environment (preferred) Extensive experience with CMC regulatory submissions and technical oversight of external manufacturing partners (CMOs/CDMOs) (preferred) Strong stakeholder and change management capabilities with experience leading complex global transformations (preferred) Proficiency in manufacturing data analytics and process modeling tools (preferred) Core Competencies Demonstrates extensive expertise in process development, validation, and regulatory compliance within pharmaceutical manufacturing, alongside strong strategic leadership and stakeholder management capabilities. Proficient in implementing advanced manufacturing technologies and digital solutions to drive operational excellence and continuous improvement. Highest-signal resume keywords Process Development Regulatory Compliance Strategic Leadership Manufacturing Data Analytics Technical Services Management Hard Skills Process Validation Technical Standards Manufacturing Platforms GMP Compliance Automation Solutions Technology Transfer Operational Excellence Capital Project Management Advanced Manufacturing Technologies Digital Technologies Soft Skills Stakeholder Management Change Management Leadership Experience Global Transformation Leadership Certifications & Qualifications BSc in Chemical Engineering MSc in Mechanical Engineering PhD in Biotechnology MBA (Preferred) Industry Keywords Pharmaceutical Manufacturing Biologics Animal Health Manufacturing CMC Regulatory Submissions External Manufacturing Partners Tools & Technologies Process Modeling Tools Manufacturing Data Analytics AI Technologies Robotics J-18808-Ljbffr

General Counsel – Sole Attorney (Chicago)

About Us The Griffin Museum of Science and Industry, Chicago is the largest and most interactive science museum in the Western Hemisphere. Chicago’s Museum of Science and Industry (MSI) expose guests of all ages to awe-inspiring exhibitions that spark curiosity and bring science to life. MSI’s mission – to inspire the inventive genius in everyone – is realized through its world-class exhibitions and engaging guest experiences. The Museum of Science and Industry provide programs and experiences that deepen the engagement of students and teachers in science and science-related disciplines, with a vision to inspire and motivate our children to achieve their full potential in the fields of science, technology, engineering and math. We offer a creative, collaborative, and innovative environment for our employees. Our employees get great perks such as: benefits starting day one of your employment, free admission to MSI for family and friends, free admission to other museums, free parking in MSI’s garage and more! If you are equally passionate about our vision and want to be surrounded by a team of dynamic, smart and innovative people, the Museum of Science and Industry is the right place for you! The Job The General Counsel leads the Museum's legal function as its sole in-house attorney, offering a unique opportunity for broad responsibility, meaningful impact, and direct engagement with senior leadership and the Board of Trustees in a fast-paced environment. The position combines functioning at both a hands‑on and strategic level, leveraging outside counsel thoughtfully to enhance internal capabilities. Responsibilities Legal Operations and Outside Counsel Management Retain, manage, and oversee outside counsel and specialized legal advisors to ensure high quality, cost-effective legal services. Lead and coordinate legal strategy for litigation, disputes, and legal proceedings involving the Museum. Contracts and Commercial Matters Review, draft, and negotiate a wide range of complex agreements across all Museum operations including: Exhibit fabrication and rentals Construction and facilities maintenance Artifact loans Intellectual property licensing Special events and education programs Fundraising and development activities Debt instruments and general commercial agreements Strategic and Executive Leadership Serve as the primary advisor to the President and CEO and senior leadership team on all legal, regulatory, and risk-related matters. Partner with executive leadership to support the Museum's mission, strategy, and business objectives while proactively identifying and mitigating legal risks. Participate in the development of organizational policies, procedures, and programs, providing ongoing guidance on legal implications. Board Governance and Ethics Serve as the General Counsel to the Board of Trustees, providing legal guidance on governance, fiduciary duties, and compliance. Act as a staff liaison to the Nominating and Governance Committee. Serve as the Museum's Chief Ethics Officer under the Code of Ethics including oversight of conflicts of interest and ethics reporting. Employment, Labor and Regulatory Compliance Advise on employment and labor matters, including union relations, collective bargaining agreements, and compliance with applicable employment laws. Ensure organizational compliance with federal, state, and local laws affecting nonprofit organizations including 501(c)(3) requirements. Risk Management and Insurance Identify and analyze legal and operational risks across the organization. Maintain and oversee the Museum's property and casualty insurance portfolio. Co‑lead the Enterprise Risk Management (ERM) program in partnership with the CFO. Intellectual Property Provide legal counsel on copyright, trademarks, and other IP matters, particularly related to marketing, advertising, education programs, and exhibit development. Cross-functional Partnership Develop a deep understanding of Museum operations and build trusted relationships across departments. Translate complex legal issues into clear, practical guidance for non‑legal stakeholders. Other duties as assigned. Qualifications Juris Doctor (JD) from an accredited law school; licensed and in good standing to practice law in the State of Illinois. Minimum of seven (7) years of relevant legal experience; significant in‑house experience and/or advising nonprofit organizations preferred. Demonstrated experience advising executive leadership and boards on governance matters. Strong background in contracts, employment and labor law, and general corporate matters. Knowledge of laws and regulations impacting 501(c)(3) organizations, preferably within a cultural, educational, or mission‑driven context. Experience managing an internal legal function and overseeing outside counsel preferred. Familiarity with intellectual property, risk management, and insurance matters preferred. Ability to be a strategic, pragmatic legal advisor with strong business acumen. Hands‑on, solution‑oriented, and comfortable operating in a fast‑paced environment. Excellent written and communication skills with the ability to explain complex legal matters clearly and concisely. Highly organized, detail‑oriented, and able to prioritize effectively amid changing demands. Demonstrated integrity, sound judgement, credibility, transparency, and a high‑level of confidentiality. Collaborative team player with a down‑to‑earth approach and strong interpersonal skills. Intellectual curiosity with the ability to quickly develop expertise in new areas of law. Language Ability to read and interpret documents such as safety rules, standard operating procedures, etc. Ability to write routine reports and correspondence. Ability to speak effectively before groups of employees of the organization. Mathematical Ability to calculate figures and amounts such as percentages, turnover rates, retention rates, etc. Reasoning Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Physical While performing the duties of this job, the employee is regularly required to use hands to finger, handle or feel and talk or hear. The employee frequently is required to stand, walk, and reach with hands and arms. The employee is occasionally required to sit; climb or balance; stoop, kneel, crouch or crawl; and taste or smell. The employee must occasionally lift and/or move up to 25 pounds. Work Environment The noise level in the work environment is usually moderate. The salary range for this position is $200,000 - $225,000. This fulltime position is eligible for benefits including: Comprehensive medical, dental, and vision plans An attractive time off program including vacation, sick, and personal days 10 Company Holidays 401(k) plans (Traditional and Roth) including a generous employer match Robust Voluntary benefit plans including transportation, legal, and many others Free onsite garage parking Position created on September 2, 2026 Our Inclusion and Belonging Statement The Griffin Museum of Science and Industry is committed to advancing diversity, equity, accessibility and inclusion across our workforce, experiences, and day‑to‑day operations. As Griffin MSI employees, we are each responsible for making the Museum a welcoming place externally for guests and internally for our colleagues within the scope of our roles. Griffin MSI is an Equal Opportunity/Affirmative Action employer, which includes providing equal opportunity without regard to race, color, religion, gender, national origin, disability, or protected veteran status. J-18808-Ljbffr