Novo Nordisk

Scientist

• Design and manage stability studies, including preparation of protocols, reports, and regulatory documentation
• Analyse stability data, identify trends, and provide scientific recommendations to support decision-making
• Support production and integrate stability considerations into manufacturing activities
• Contribute to investigations, deviations, and regulatory submissions related to stability
• Drive continuous improvement initiatives and identify opportunities to optimise processes
• Assess the necessity and evaluate the outcomes of stability studies
• Support stability activities for life-cycle management products and products transitioning from development to production

Development Scientist

Operator

• Perform all aspects of truck and bulk liquid unloading to support API-US facility operations
• Load and unload products from trucks, tankers, and ISO containers
• Operate pumps and valves; blend and mix chemicals and products as needed during offloads
• Handle, label, and store hazardous and non-hazardous materials
• Perform material handling operations for hazardous materials in drums, pallets, and IBC configurations
• Ensure timely and accurate material movements in SAP/ERP
• Perform visual and pH inspections on rainwater before pumping out containment areas as needed
• Perform weekly pH probe calibrations using MES/DeltaV
• Replace solvent and boundary filters according to planned maintenance schedules in SAP
• Partner with warehouse sampling operations to complete tasks
• Conduct daily inspections of equipment used for chemical and material offloading
• Adhere to plant health, safety, and environmental guidelines, policies, and procedures
• Keep the work area clean throughout the shift
• Maintain up-to-date training status
• Work in a safe and environmentally responsible manner
• Perform other assigned accountabilities
• Report to the Manager, RMS & Utilities Operations

Hazmat Control Operator I

Recruitment

• Own end-to-end recruitment across a varied portfolio of roles and guide and challenge hiring managers
• Provide timely, value-adding recruitment advice
• Keep candidates and hiring managers informed and supported throughout the recruitment process
• Apply market insight to shape sourcing, assessment and selection
• Champion inclusive hiring in line with diversity and inclusion objectives
• Safeguard data integrity and compliance
• Ensure local stakeholders follow the Global Standard TA process while meeting local requirements
• Propose improvements based on stakeholder collaboration and external best practice
• Support global initiatives or projects when needed
• Work with hiring managers, HR Business Partners, Centres of Excellence, Global People & Organization Services, candidates and recruitment agencies
• Own talent acquisition matters within scope, safeguard the employer value proposition and escalate complex or cross-functional issues

Talent Acquisition Partner

Student

• Support CRAs with activities related to trial start-up, conduct and close-out
• Prepare, quality-check, maintain and archive trial documentation and site materials in line with quality and compliance requirements
• Coordinate, track and ship clinical trial equipment, patient materials and study supplies to clinical sites
• Support reporting, meeting preparation, documentation and follow-up across trial teams
• Assist with administrative processes such as purchase orders and payments
• Contribute to selected ad hoc projects and continuous improvements across CDC DK
• Work closely with Clinical Research Associates, Trial Managers, Clinical Trial Assistants and other cross-functional colleagues
• Report to the Clinical Operations Manager, CDC DK

Student Assistant

• Manage a varied portfolio of roles across different levels of complexity
• Own end-to-end recruitment and advise and challenge hiring managers
• Keep candidates and hiring managers informed and supported throughout the recruitment process
• Apply market insight to shape sourcing, assessment and selection
• Champion inclusive hiring in line with diversity and inclusion objectives
• Safeguard data integrity and compliance
• Ensure local stakeholders follow the Global Standard TA process while meeting local requirements
• Propose improvements based on stakeholder collaboration and external best practice
• Support global initiatives or projects as needed
• Work with hiring managers, HR Business Partners, Centres of Excellence, Global People & Organization Services, candidates and recruitment agencies
• Operate with autonomy, own TA matters within scope, protect the employer value proposition, and escalate complex or cross-functional issues

Data Scientist

• Manage assigned clinical-trial tasks, including SDTM and ADaM deliverables, annotated CRFs, SDTM datasets, ADaM programming, and TFLs
• Contribute to trial setup through eCRFs, Data Flow Plans, metadata specifications, mock TFLs, SDRG, ADRG, and Define.xml
• Support CSRs, RMPs, IBs, DSURs, PSURs, and public disclosure deliverables
• Collaborate with CROs, regulatory authorities, internal stakeholders, and scientific communities
• Share best practices and contribute to process optimization and change management
• Provide training and support on statistical computing environments, system usage, and SOPs
• Ensure documentation and programming comply with GCP, GDP, and GPP standards

Senior Clinical Data Scientist

• Support process development, technology transfer, process implementation, validation, and process optimisation activities for synthetic peptides throughout the product life cycle
• Act as subject matter expert for synthetic peptide manufacturing processes
• Support technology transfer, validation activities, and lifecycle management initiatives
• Provide scientific and technical support to CMOs and manufacturing sites
• Troubleshoot, handle deviations, optimise processes, and implement process improvements
• Serve as process and product owner for SPPS-based peptide manufacturing processes
• Prepare and review technical and GMP documentation for validation, regulatory submissions, process changes, and lifecycle management
• Support assessment, onboarding, and implementation of new CMOs
• Collaborate with Late-Stage Development, Analytical Functions, Quality Assurance, Regulatory Affairs, Global Contract Manufacturing, Sourcing, pilot facilities, production sites, and external partners
• Travel approximately 10–20 days annually

Director

• Lead global outsourcing activities and manage CMO collaborations
• Manage outsourcing projects within oral and injectable drug product solutions from initiation to completion
• Select and approve CMOs
• Negotiate and maintain relevant agreements with Contract Managers
• Build strong, collaborative external partnerships
• Protect Novo intellectual property rights
• Ensure timely delivery of high-quality assessments
• Facilitate cross-organisational collaboration across Global Research, Quality, Regulatory, Purchasing, Manufacturing Development, and Commercial Manufacturing
• Drive outsourcing projects and day-to-day CMO collaboration at Senior Outsourcing Manager level
• Provide broader strategic leadership on complex partnerships and cross-functional decision-making at Associate Outsourcing Director level
• Influence decisions, drive progress, and lead complex projects through informal leadership

Senior Outsourcing Manager / Associate Outsourcing Director

Research Engineer

• Lead the technical direction of end-to-end digital products
• Design and develop applications using modern technologies, analyzing, integrating, and leveraging existing solutions
• Define architecture across applications, integration, data, search, and cloud layers
• Establish observability, security, quality, and relevant engineering practices
• Collaborate with researchers, product managers, data engineers, software engineers, and cross-functional stakeholders
• Balance innovation, scalability, security, and business value
• Improve and extend the existing digital product, including adding new data sources
• Deliver platform-focused proofs of concept and infrastructure solutions, including Kafka plugins and AWS MSK
• Drive software solutions from early proofs of concept to enterprise-grade production systems

Lead Software Engineer – Research Tech Delivery, AI & Digital Innovation

Operations

• Conduct medical interpretation and evaluation of adverse events from clinical trials and post-marketing surveillance
• Ensure compliance with global regulatory requirements for collection, evaluation, and expedited reporting of serious adverse events to health authorities
• Perform medical reviews and causality assessments of serious adverse events
• Determine potential relationships between serious adverse events and Novo Nordisk products
• Participate in clinical project teams from protocol design through trial conduct
• Lead cross-functional groups and chair safety meetings
• Establish improved methods and share best practices to enhance safety deliverables and ensure accurate MedDRA coding
• Train investigators, clinical safety associates, and affiliate partners on safety data handling and adverse event management
• Collaborate with Global Development, Regulatory Affairs, Data Management, and affiliates worldwide

Safety Operations Advisor

Medical Liaison

• Build relationships and demonstrate the clinical outcomes and benefits of Novo Nordisk products
• Provide medical information and educate healthcare providers and relevant organizations
• Coordinate education workshops and provide product and scientific updates
• Serve as a scientific liaison between Novo Nordisk and external customers
• Provide advanced product, scientific, and medical field support to Medical, Sales, Marketing, Managed Care, and Government teams
• Represent the organization externally to clinicians, professional societies, academic medical centers, integrated delivery networks, managed care organizations, and other healthcare organizations
• Complete administrative duties, manage regional operations and budgets, and submit monthly scientific support reports
• Attend and present at medical and scientific meetings
• Develop relationships with healthcare providers, investigators, academic centers, and key formulary influencers
• Establish medical account strategies and gather customer insights on Novo Nordisk and competitor products
• Identify and recruit qualified investigators for company-sponsored activities
• Prepare training materials and review sales representative training
• Mentor new or junior Field Medical Affairs colleagues
• Collaborate with Sales, Marketing, Medical, Clinical Research Associates, and other internal stakeholders
• Provide clinical education and support to integrated health networks and formulary stakeholders
• Coordinate and facilitate clinical studies, including site initiation, patient recruitment and retention, and study completion
• Develop and present product, scientific, and formulary updates
• Facilitate submission of pharmacoeconomic, outcomes research, and investigator-sponsored studies

Medical Liaison – Portfolio

Manager

• Align field marketing strategies with sales objectives to enhance healthcare professional engagement and key account prioritization
• Develop effective field communications
• Coordinate with training for new product launches
• Manage marketing campaigns and coordinate successful product launches
• Develop the US commercial launch strategy with the marketing launch team
• Provide leadership oversight for pre-launch and launch strategic and tactical brand plans aligned with global marketing
• Conduct market analysis and market research
• Develop customer- and patient-centric programming, HCP and patient marketing tactics, and market-shaping initiatives
• Support KOL development, advisory boards, clinical communications and medical education programs
• Align marketing strategies with field team objectives and oversee promotional campaigns across digital and in-person channels
• Gather cross-functional insights on market trends and customer feedback to enhance field sales activities
• Develop and distribute field communications and conduct training on product launches, clinical data updates and marketing messaging
• Oversee product sample distribution and tracking in compliance with regulations and company policies
• Collaborate with supply chain and sales teams to optimize sample inventory
• Support rollout of branded and unbranded promotional materials and marketing-led campaigns
• Coordinate and execute product launch meetings and develop launch materials and presentations
• Ensure field teams have pre- and post-event engagement tools
• Apply market insights to identify growth opportunities and support brand strategy, competitive defense and strategic evolution
• Advocate for US marketing initiatives within global marketing

Senior Field Engagement Manager

• Facilitate project execution and project controls
• Lead tactical and long-term production processes and strategic activities
• Manage operational aspects of projects, including cost, quality, and schedule requirements
• Build and maintain the operations team
• Lead activities to drive operational performance and process/technical improvements
• Maintain team standardization
• Ensure employee engagement, motivation, and development
• Drive a safe workplace culture and ensure safety and environmental requirements are met
• Ensure robust processes exceed quality objectives, specifications, and requirements
• Drive shift project performance to meet business and stakeholder needs
• Eliminate issues and simplify processes
• Align process activities with lead-time targets and site goals
• Drive process performance to meet business and customer needs
• Drive operational standardization and collaboration with other shift teams
• Operate the process in a cLEAN® way
• Manage personnel issues, hiring/firing, and vacation planning for shift team members
• Coach, develop, and engage direct reports
• Integrate quality and business ethics into decisions
• Confirm project and process standards
• Establish individual development plans, goals, measurements, learning plans, and aspiration plans for reporting personnel
• Manage the application and communication of Novo Nordisk policies, procedures, and Novo Nordisk Way
• Report to the Senior Manager, Operations

Manager, Shift Operations

Executive Assistant

• Provide comprehensive administrative support to the Site Head and Senior Leadership Team
• Represent the executive team professionally while maintaining strict confidentiality
• Identify, drive, plan, execute, and report on projects within scope, cost, and time constraints
• Guide senior leadership through Novo Nordisk systems and processes
• Manage the Site Head’s calendar, resolve conflicts, schedule meetings, arrange travel, and coordinate logistics
• Plan and coordinate large meetings, international meetings, group events, and facility tours
• Prepare agendas, presentations, reports, meeting minutes, and follow-up documentation
• Review, prioritize, and act on incoming communications
• Partner with internal communications to prepare site communications and announcements
• Collaborate with P&O on site initiatives, engagement, and NNWay facilitation
• Maintain extensive knowledge of the West Lebanon facility, including shift schedules, management team, and organizational structure
• Support the Site Head and family on international mobility assignment matters when applicable
• Serve as an anchor and resource for the Site Head and Senior Leadership Team
• Drive and own the shared agenda for administrative assistants; assign work, review work, and provide training, assistance, and mentoring
• Arrange catering, expense reporting/approval, town hall events, facility tours, and visitor logistics
• Perform duties in a compliant and ethical manner in accordance with applicable healthcare laws, regulations, and industry codes
• Incorporate the Novo Nordisk Way and 10 Essentials into activities and interactions

Backend Engineer

• Provide routine support and troubleshooting for the manufacturing facility
• Provide input, review, and approve design and requirement documents
• Provide input, review, and approve technical specifications
• Support development of design and requirement specification documents
• Support equipment and process quality
• Support creation of process-track risk assessment documents, including Requirement Risk Assessments
• Participate in creation of project cGMP Statements
• Create and participate in Quality Risk Management risk assessments, including Closed-Process, Cross-Contamination, Contamination, and Facility Flows
• Complete self-development activities and partner with the manager to understand development needs
• Provide input to and review Process FMECA documents
• Participate in design workshops with engineering suppliers
• Provide input to and review Process Module Diagrams and Process Flow Diagrams
• Provide input to and review Process Scheduling and Capacity Calculations
• Support package maintenance of schedule adherence
• Ensure coordination and collaboration between the project and site stakeholders
• Gather and ensure knowledge transfer to the project from the Denmark sponsor site
• Follow all safety and environmental requirements
• Perform other duties as assigned

Development Scientist

Hazmat Control Operator I

Talent Acquisition Partner

Student Assistant

Talent Acquisition Partner

Senior Clinical Data Scientist

Development Scientist

Senior Outsourcing Manager / Associate Outsourcing Director

Lead Software Engineer – Research Tech Delivery, AI & Digital Innovation

Safety Operations Advisor

Medical Liaison – Portfolio

Senior Field Engagement Manager

Manager, Shift Operations

Executive Assistant

Associate Process Engineer – API, Recovery