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You will support regulatory strategies for device components of combination products, engage in submission planning, ensure cross-functional alignment, and represent regulatory affairs in project teams. The role also involves communication with health authorities and contributing to regulatory strategy throughout product development.
The Global Director, Commercial Partnerships at Novo Nordisk is responsible for evaluating and managing commercial partnerships, leading end-to-end project execution, negotiations, and ensuring strategic alignment for the company's global commercial strategy.
The Associate Project Director will lead the development of human cell-based disease models for drug discovery in cardiometabolic diseases, collaborate with multidisciplinary teams, and establish scientific direction for the new department.
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The Manager of Quality Support will lead the Packaging Quality Support team, focusing on employee well-being, improving processes, managing supplier-related issues, and maintaining operational performance. The role requires significant experience in quality work and fostering a collaborative environment.
The Manager for Packaging Material Supply Planning will oversee a team of planning professionals to ensure the supply of primary packaging across manufacturing sites. Responsibilities include optimizing processes, problem-solving for operational errors, leading KPI meetings, fostering team well-being, and building stakeholder relationships.
The Global Strategy Project Lead will develop and implement Digital Health strategies for Novo Nordisk, collaborating with brand and clinical teams. You will prioritize portfolio strategies, build networks with stakeholders, and communicate strategies at all organizational levels to drive impactful health outcomes for patients and healthcare professionals.
As a Chemical Health & Safety Expert, you will provide technical leadership on chemical safety, develop chemical management agendas, support risk assessments, ensure compliance with regulations, review project deliverables, and manage global training programs for chemical handling.
The Senior Manager will ensure compliance with the Drug Supply Chain Security Act (DSCSA), managing serialization and exception handling processes. This role supports projects, coordinates IT solutions for Supply Chain Operations, and collaborates with various teams and vendors to enhance DSCSA processes and ensure effective data exchange.
The Global Market Access Policy Director will lead engagement on market access policies and legislation, providing strategic recommendations based on global insights. The role involves internal briefings for management and external representation at industry conferences and stakeholder meetings, aimed at enhancing patient access to innovative medicines.
As a Regional Medical Advisor, you will facilitate communication of scientific data among medical experts in Croatia, manage medical activities, develop educational programs, and build relationships within the healthcare sector to promote diabetes and obesity management. You will ensure compliance with regulations while serving as a scientific ambassador for the company.
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