Chief Executive Officer (New York)

About the role Portfolio Scope The CEO leads B Lab as the primary architect of its unified future - translating Board direction into a clear vision and coherent operating model, and stewarding the mission across the global network. This role goes beyond conventional CEO functions by explicitly championing network health as a strategic priority - ensuring the CEO Office dedicates appropriate attention to fostering collaboration across B Lab's complex structure. As B Lab's principal external voice, the CEO also represents the organisation on the global stage, building credibility with business leaders, funders, policy makers and multilaterals. The CEO holds ultimate accountability for vision, strategy, culture, and the ongoing network integration, creating the conditions for the organization to deliver B Lab's Theory of Change and contribute to economic transformation. Transformation Context B Lab is undergoing two simultaneous transformations: the evolution of its standards and assurance model, and the unification of its network into one global organisation. The CEO must navigate this complexity while energising leaders and teams. This role requires bringing calm and confidence while maintaining momentum on critical strategic initiatives and building a vision for the future. The CEO must ensure that integration enhances rather than constrains B Lab's ability to drive systems change, building trust that the new unified structure will strengthen mission and impact. Leading through this transformation demands exceptional emotional intelligence, strategic clarity, and the ability to hold space for both organizational change and excitement about the future. Mission Connection The CEO embodies B Lab's Theory of Change by orchestrating how the organization drives behavior change in business, grows a movement and scales the cultural and structural change needed to transform the economic system. As the primary steward of the mission, the CEO ensures that every portfolio - from standards to technology, from markets to movement building - works in concert to create an economy that works for all people and the planet. This role must articulate and evolve B Lab's vision in ways that inspire diverse stakeholders while maintaining operational discipline. The CEO demonstrates that organizational effectiveness and impact are mutually reinforcing dynamics. Through strategic leadership and cultural stewardship, the CEO helps B Lab model the interdependence and care it seeks to create in the world. Compensation This is a truly global role and compensation may differ depending on the location in which the successful candidate is based. BLab has gathered equitable salary insights for each region of opera J-18808-Ljbffr

Chief Operations Officer - The Innovation Space (Wilmington)

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it’s providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world’s most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers About the Innovation Space Every day, scientists and entrepreneurs at The Innovation Space are working to turn promising discoveries into companies and solutions to change the world for the better with the potential to improve lives, strengthen industries, and address important global challenges. The Innovation Space is a nonprofit organization and entrepreneurial ecosystem that helps science-based startups transform breakthrough technologies into commercially viable businesses. Located on the historic Experimental Station campus in Wilmington, Delaware, The Innovation Space provides an integrated platform of laboratory and office facilities, shared scientific equipment, entrepreneurial programs, expert mentorship, funding opportunities, and connections to investors and strategic partners. Established through a public-private partnership among the State of Delaware, DuPont, and the University of Delaware, The Innovation Space supports entrepreneurs working across life sciences, industrial biotechnology, advanced materials, clean technology, renewable energy, nutrition, and related fields. Its collaborative ecosystem brings together scientists, entrepreneurs, business leaders, investors, and service providers to accelerate commercialization, company growth, and real-world impact. The Innovation Space is a collaborative, mission-driven, and entrepreneurial organization. Our work moves quickly, priorities evolve, and team members regularly contribute beyond traditional functional boundaries. We value curiosity, sound judgment, mutual respect, practical problem-solving, and a shared commitment to helping entrepreneurs succeed. Since 2017, over 160 companies supported by The Innovation Space have raised more than $1.24 billion in capital. In 2025, The Innovation Space and its portfolio of startups supported approximately 2,490 jobs and generated an estimated $703.9 million in economic output nationwide. Learn more at www.innovationspace.org. About the role The Chief Operations Officer leads the laboratory, facilities, scientific support, and business operations that enable The Innovation Space and its client companies to succeed. Reporting operationally to the President & CEO, the COO translates organizational strategy into safe, reliable, and scalable systems across facilities, finance, legal, technology, people operations, EH&S, compliance, and risk management. This highly visible role combines enterprise leadership with hands‑on execution and offers the opportunity to help scientists and entrepreneurs advance breakthrough technologies toward commercial and societal impact. The COO leads a capable multidisciplinary team with four direct reports: the Client Experience Manager, Assistant Director of Facilities, Senior Scientist and Laboratory Manager, and Laboratory Coordinator. The COO also draws upon specialized expertise from DuPont and an established network of external financial and legal advisors, contractors, and service partners. This combination of internal capability and external support enables the COO to provide enterprise-level leadership, delegate effectively, and remain sufficiently close to day‑to‑day execution to engage directly when needed. The COO will be a DuPont employee seconded to The Innovation Space. The President & CEO of The Innovation Space will provide day‑to‑day direction, establish organizational priorities, and oversee performance in the role, while DuPont will retain responsibility for employment administration. This is an opportunity to help shape a nationally significant center for science‑based entrepreneurship. The COO will work alongside scientists, founders, investors, corporate leaders, and public‑sector partners advancing new solutions across health, biotechnology, advanced materials, clean technology, energy, and nutrition. Key Responsibilities Laboratory, Facilities, and Client Service Delivery Provide overall leadership for the organization’s 130,000-square-foot laboratory, office, and collaboration facility, ensuring safe, reliable, and cost-effective delivery of infrastructure, technical capabilities, and services. Lead laboratory and facility planning, infrastructure reliability, preventive maintenance, capital planning, and significant construction and improvement projects. Manage operating budgets and external contractors, vendors, and service providers supporting laboratory and facility operations. Partner with Innovation Space clients to understand their operational and technical needs and continually improve laboratory capabilities, service quality, reliability, utilization, and the overall client experience. Business, Financial, Grant, and Contract Operations Oversee budgeting, forecasting, accounting, cash management, financial reporting, audits, tax coordination, and internal financial controls, working closely with the President & CEO and external financial resources. Lead annual operating and capital planning and support financial reporting to organizational leadership, the Board of Directors, funding partners, and government agencies. Oversee the administrative and financial management of government, foundation, and corporate grants, including budgeting, compliance, allowable-cost requirements, documentation, reporting, audit readiness, and coordination with program leaders. Lead the development, review, negotiation, and administration of client agreements, collaboration agreements, grant and funding agreements, vendor contracts, and construction and capital-project agreements, working with legal counsel as appropriate. Oversee procurement, competitive bid processes, vendor selection and management, insurance, contract tracking, and other core business administration activities. Provide strategic oversight of information technology, cybersecurity, telecommunications, access-control systems, financial systems, and other business technology infrastructure. EH&S, Compliance, and Risk Management Provide leadership for environmental health and safety, laboratory safety, regulatory compliance, and enterprise and operational risk management. Establish and maintain appropriate policies, procedures, management systems, and internal controls to support safe, compliant, and effective operations. Oversee regulatory interactions, environmental reporting, audits, inspections, emergency preparedness, business continuity, and corrective actions. Startup Sourcing, Due Diligence, and Funding Programs Support the sourcing and recruitment of promising science‑based startups through relationships with universities, investors, accelerators, economic‑development organizations, corporate partners, and other ecosystem stakeholders. Lead or coordinate due diligence on prospective client companies and applicants to Innovation Space investment, grant, and acceleration programs. Evaluate company leadership, technology and intellectual property, market opportunity, business model, development milestones, financing strategy, operational requirements, and key execution risks. Support the First Fund investment program and Early‑Stage Growth Grants through pipeline development, application review, diligence, funding recommendations, agreement development, closing, milestone tracking, and post‑award monitoring. Leadership, People, and Strategy Partner with the President & CEO and leadership team to establish organizational priorities and translate strategy into operating plans, budgets, systems, capabilities, and measurable results. Lead and develop a multidisciplinary team of employees, contractors, and external service providers across a broad range of technical, financial, and business functions. Build effective relationships across the Innovation Space ecosystem, including DuPont, the University of Delaware, government and funding partners, clients, investors, vendors, and other stakeholders. Proactively identify organizational risks, resource constraints, and opportunities for improvement and lead cross‑functional solutions. Partner with program leadership on grant‑funded initiatives and lead other strategic projects at the direction of the President & CEO. Key Qualification Profile Required Bachelor’s degree in science, engineering, operations, or a related field, or equivalent relevant experience. At least 10 years of progressively responsible operational leadership experience, including leadership of multidisciplinary teams. Experience overseeing complex laboratories, research, engineering, manufacturing, or similarly regulated operations. Demonstrated financial acumen and responsibility for operating budgets, capital planning, financial performance, financial statements, internal controls, vendor management, and contract administration. Experience providing executive oversight of EH&S, regulatory compliance, operational risk, emergency preparedness, and business continu

Vice President of Direct Marketing Direct Marketing Direct Marketing Pleasant Prairie, Wisconsin 2026-08-27 00:00:00Z 26 R266736 Pay Based on Qualifications (Northern)

Vice President of Marketing Corporate Headquarters 12575 Uline Drive, Pleasant Prairie, WI 53158 Lead strategy. Shape investment. Drive growth. Uline is seeking a Vice President of Marketing to lead one of North America's largest print marketing programs, shaping customer engagement across 45,000 products. Develop leaders across the department, oversee significant marketing investments and partner with executive leadership committed to long-term growth. Position Responsibilities Direct one of North America's largest print marketing programs, shaping strategy for catalogs, direct mail and print communications for 45,000 products. Lead and develop director s and managers across campaign execution, audience targeting, procurement, distribution and quality assurance to ensure high performance. Oversee print production, paper sourcing and postage operations, driving efficiency, optimizing costs and improving program effectiveness. Build strategic partnerships and negotiate agreements with print, paper, mailing and data vendor s to ensure exceptional quality, service and value. Partner with executive leaders across Creative, Merchandising, Sales and Finance to align print marketing initiatives and o versee $500M annual investment. Minimum Requirements Bachelor’s degree in Marketing, Advertising, Business or related field. MBA preferred. 15 years of leadership experience in catalog publishing, print marketing, direct mailor marketing operations. 10 years of experience leading managers and cross-functional teams in a fast-paced business environment. Proven success negotiating vendor contracts, managing large-scale budgets and improving operation al efficienc y. Benefits Complete health insurance coverage and 401(k) with 6% employer match that starts day one! Multiple bonus programs. Paid holidays and generous paid time off. Tuition Assistance Program that covers professional continuing education. Employee Perks On-site café and first-class fitness center with complimentary personal trainers. Over four miles of beautifully maintained walking trails. About Uline Uline, a family-owned company, is North America’s leading distributor of shipping, industrial, and packaging materials with over 10,000 employees across 1 5 locations. Uline is a drug-free workplace. All new hires must complete a pre-employment hair follicle drug screening. All positions are on-site. EEO/AA Employer/Vet/Disabled Our employees make the difference and we are committed to offering exceptional benefits and perks!Explore Uline.jobs to learn more! J-18808-Ljbffr

Vice President, Medical Affairs, Clinical Operations & Regulatory Affairs Seal Beach, California, United States (Seal Beach)

Vice President, Medical Affairs, Clinical Operations & Regulatory Affairs Seal Beach, California, United States WHO WE ARE : At Dendreon,we’retransforming the battle against cancer with personalized immunotherapy. Our flagship product, PROVENGE® (sipuleucel-T) , was the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer,utilizinga patient’s own immune cells to fight the disease. If you’re driven by the opportunity to make a meaningful impact on cancer patients’ lives, we invite you to join our team. With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a talented team of scientific, clinical, regulatory, and corporate professionals based in Seal Beach, and a commercial organization operating across the United States, Dendreon continues to advance innovation in personalized cancer treatment. CORE VALUES: Put Patients First: Every day is an opportunity to improve the lives of those living with cancer. Act with Integrity: We commit to transparency, honesty, and always doing what’s right. Build Trust: Trust is earned through candid, open communication and a collaborative approach. Raise the Bar: We embrace continuous improvement and innovation, always striving to elevate our people. Drive Results: We are accountable to each other and deliver success together. WHO WE ARE : At Dendreon, we’re transforming the battle against cancer with personalized immunotherapy. Our flagship product, PROVENGE® (sipuleucel-T) , was the first FDA-approved immunotherapy for metastatic castrate-resistant prostate cancer,utilizinga patient’s own immune cells to fight the disease. If you’re driven by the opportunity to make a meaningful impact on cancer patients’ lives, we invite you to join our team. With Immunotherapy Manufacturing Facilities in Seal Beach, CA, and Union City, GA, a talented team of scientific, clinical, regulatory, and corporate professionals based in Seal Beach, and a commercial organization operating across the United States, Dendreon continues to advance innovation in personalized cancer treatment. CORE VALUES: Put Patients First: Every day is an opportunity to improve the lives of those living with cancer. Act with Integrity: We commit to transparency, honesty, and always doing what’s right. Build Trust: Trust is earned through candid, open communication and a collaborative approach. Raise the Bar: We embrace continuous improvement and innovation, always striving to elevate our people. Drive Results: We are accountable to each other and deliver success together. NOTE: This role requires on-site presence at our Seal Beach, CA location. Responsibilities: Medical Affairs Leadership (50%) Provide strategic oversight of Medical Affairs activities to ensure alignment between clinical development, regulatory strategy, and commercial objectives. Partner with Commercial leadership to ensure scientifically accurate and compliant communication regarding company products and pipeline programs. Develop and maintain strategic relationships with physicians, investigators, Key Opinion Leaders (KOLs), healthcare providers, and scientific experts to support clinical development, evidence generation, product adoption, and medical education initiatives. Support development and review of scientific and medical content, including publications, congress presentations, medical education materials, and field medical resources. Oversee medical review of promotional and non-promotional materials to ensure scientific accuracy and regulatory compliance. Collaborate with Key Opinion Leaders (KOLs), investigators, and external scientific experts to support product development and lifecycle management. Support investigator-sponsored studies (ISS), real-world evidence initiatives, and post-marketing clinical activities. Provide medical and scientific leadership during regulatory submissions, advisory board meetings, and agency interactions. Ensure appropriate collection and communication of medical insights from healthcare providers and clinical stakeholders. Clinical Operations Leadership (30%) Provide strategic oversight for the planning, execution, monitoring, and reporting of clinical trials. Lead Clinical Operations teams, CROs, vendors, and study partners to ensure successful delivery of clinical programs. Develop and implement clinical operational strategies that align with regulatory and corporate objectives. Oversee study timelines, budgets, resource allocation, and risk management activities. Ensure clinical studies are conducted in compliance with GCP, ICH guidelines, protocol requirements, and applicable regulations. Collaborate with Medical Affairs, Regulatory Affairs, Quality, Biostatistics, Data Management, and Pharmacovigilance functions. Monitor study performance metrics and implement corrective actions when necessary. Support clinical site selection, startup activities, enrollment strategies, and study closeout activities. Ensure inspection of readiness and support regulatory inspections and audits. Drive continuous improvement initiatives to enhance operational efficiency and study execution. Regulatory Affairs Leadership (20%) Develop and execute global regulatory strategies supporting product development, clinical studies, manufacturing changes, and commercialization initiatives. Lead preparation, submission, and maintenance of regulatory filings, including INDs, BLAs, amendments, supplements, annual reports, and other regulatory submissions. Serve as the primary liaison with regulatory agencies, including the U.S. Food and Drug Administration and international health authorities. Provide regulatory guidance and risk assessments to executive leadership, project teams, and functional departments. Ensure compliance with applicable regulations, guidance documents, and industry standards. Monitor evolving regulatory requirements and assess business impact. Lead regulatory interactions, meetings, inspections, audits, and responses to agency inquiries. Support due diligence activities, licensing opportunities, partnerships, and strategic business initiatives. Establish and maintain regulatory policies, procedures, and best practices. Oversee regulatory intelligence activities and communicate emerging trends to leadership. Serve as a member of the senior leadership team, contributing to corporate strategy and organizational growth initiatives. Directly and indirectly manages Regulatory Affairs and Clinical Operations personnel, including directors, managers, individual contributors, consultants, and external service providers. Responsible for hiring, performance management, coaching, succession planning, and organizational development. Build, develop, and mentor high‑performing Regulatory Affairs and Clinical Operations teams. Establish departmental objectives, budgets, KPIs, and long‑term strategic plans. Foster strong cross‑functional collaboration across Research, Development, Manufacturing, Quality, Medical Affairs, Commercial, and Executive Leadership teams. Present program updates, regulatory strategies, and clinical development plans to executive management, board members, and external stakeholders. Manage departmental budgets and external vendor relationships. Promote a culture of compliance, accountability, innovation, and operational excellence. Partner with Pharmacovigilance and Quality teams regarding product safety communications and risk management activities. JOB REQUIREMENTS: Required Experience & Skills: Advanced degree required (MS, PharmD, PhD, MD, or equivalent scientific discipline). Medical degree preferred but not required. Additional business or leadership training preferred. Minimum 15 years of progressive leadership experience within biotechnology, pharmaceutical, cell therapy, oncology, immunotherapy, or related life sciences industries. Minimum 10 years of experience leading Regulatory Affairs functions. Significant experience overseeing Clinical Operations and clinical trial execution. Experience managing Medical Affairs activities, scientific communications, and KOL engagement. Demonstrated success leading regulatory submissions and agency interactions. Experience supporting products through development, approval, commercialization, and lifecycle management. Previous executive or senior leadership experience preferred. Expert knowledge of FDA regulations, ICH guidelines, GCP, GMP, and applicable global regulatory requirements. Strong understanding of clinical development, clinical trial operations, and evidence generation. Comprehensive knowledge of Medical Affairs functions, publication strategy, and scientific communications. Exceptional leadership, organizational, and strategic planning skills. Strong presentation, negotiation, and stakeholder management capabilities. Proven ability to influence across multiple functions and executive leadership levels. Experience managing external vendors, CROs, consultants, and scientific advisory boards. Demonstrated ability to operate effectively in a highly regulated biotechnology or pharmaceutical environment. Working Conditions and Physical Requirements: