Novo Nordisk

Security Analyst

• directly participates in Global Security Operations activities including prevention, detection, and response to IT security incidents worldwide.
• support a wide range of IT security activities including monitoring of alerts, investigation of alerts, incident response, vulnerability response, threat intelligence, and digital forensics.
• assist with the implementation of IT security strategy and serving as a security advisor.
• demonstrate expertise of current enterprise technologies and perform technical risk and vulnerability assessments at the network, system, and application level.
• develop and implement security controls and formulate operational risk mitigations.
• provide guidance and training to less experienced professionals or support staff.
• engage in frequent internal and cross-organizational contact.

Security Analyst III

Director

• The Director, HEOR Evidence Synthesis is part of the HEOR Evidence Synthesis and Strategy (HEOR-ESS) sub-team
• Serves as the HEOR evidence synthesis lead ensuring that HEOR evidence generated internally and externally is leveraged to support pre-launch, launch and life-cycle management of therapies.
• Work closely with the HEOR Strategy Director to ensure that stakeholder evidence needs are incorporated in the HEOR strategy
• Ensure scientific rigor and alignment to NNI strategy throughout product life cycle
• Monitor and engage with external bodies such as ICER, conducting health technology reviews
• Serve as an internal reviewer/approver of research protocols
• Enable pull-through of synthesized evidence for proactive and reactive communication with external customers.
• Lead the execution and dissemination of rapid data analytics requests from stakeholders to support internal strategy.
• Collaborate with various teams to lead the conceptualization and delivery of the Evidence Synthesis Package and other creative evidence deliverables
• Accountable for study specific pull through and dissemination activities including development timelines, budget, deliverables, and training

HEOR Evidence Synthesis Director

Research Analyst

• Drives understanding and delivery of quality clinical research for all monitoring and site management activities
• Takes ownership to deliver upon near-term USO Clinical Development (CDO) goals, including successful delivery of studies within the clinical trial portfolio
• Delivers all relevant services/tasks in support of the planning and implementation of quality-driven clinical trials, in line with established targets and strategies
• Implements proactive risk identification and mitigation planning for assigned clinical trial sites
• Verifies safety reporting and the proper handling, monitoring and storage of trial products
• Ensures accuracy, validity and completeness of data collected at clinical trial sites
• Develops therapeutic area knowledge sufficient to support role and responsibilities
• Drives recruitment and retention strategies to support clinical trial sites to meet country enrollment and retention targets
• Participates in the preparation, conduct and follow-up of audit and inspection activities

Clinical Research Associate

Outside Sales

• Serve as a strategic performance and leadership development partner to an assigned Area Commercial Lead (ACL) and their leadership team.
• Enable sustained behavior, change and performance through performance consulting, leadership development, instructional design, and effective delivery.
• Translate enterprise and commercial strategy into field-ready leadership capabilities, coaching standards, and development experiences.
• Accountable for designing scalable leadership development solutions, defining “what good looks like,” and ensuring capability initiatives result in measurable behavior change and improved performance.
• Act as a trusted advisor and center of expertise for leadership capability, coaching quality, and performance enablement.
• Partner closely with the ACL, P&O/Employee Experience, and cross ‑ functional stakeholders to drive consistency, accountability, and sustained impact at scale.
• Engage extensively with Sales Leadership and Commercial Execution teams across the Cardiometabolic Sales organization.
• Collaborate cross ‑ functionally with Digital & AI Enablement, Legal, Ethics & Compliance, Market Access, and Marketing partners.

Associate Director, Field Sales Capabilities

Software Engineer

• Act as the authority for safe work permitting for the facility
• Subject Matter Expert on Work Permitting Process (Permit Vision)
• Identify & implement CPO process improvements
• Support technical training of other team members (4P qualified)
• Monitor Permit Vision for work requests and process through the permit life cycle including review/approve/issue permits, review/approve/execute ICCs (LOTO), and review/approve Flush & Drain Plans
• Ability to work independently with minimal supervision
• Author ICC’s & Flush/Drain Plans
• Provide lead direction & support to junior team members
• Recognize the conditions of work that require Lockout/Tagout
• Assess all hazardous energy sources including electrical, mechanical, hydraulic, pneumatic, chemical, thermal, and other sources in machines, equipment, and systems which can be hazardous to employees & other stakeholders onsite
• Use documented procedures and approved isolation devices to implement Lockout/Tagout
• Support adherence to key elements of OSHA regulations known onsite as the Ten Life Safety Rules
• Support adherence to all Quality & Environmental & EHS regulations within area of responsibility
• Continuous process improvement using cLEAN concepts
• Establish & maintain standards & operational procedures for the Central Permit Office
• Work daily with computer programs to perform tasks (Microsoft office suite, CMMS (SAP), Permit Vision, Robex, etc.)
• Follow all safety and environmental requirements in the performance of duties

Engineering Technician II

• Strategic HR Leader and member of R&D P&O Leadership Team
• Charged with executing the strategic P&O agenda for R&D P&O globally
• Leading a team of experienced HR Business Partners and P&O Professionals
• Collaborating across Novo Nordisk R&D units globally, regionally and locally
• Accountable for driving the P&O strategy and HRBP delivery within teams

Director, P&O R&D, Global Sites

Engineer

• Create & maintain system specifications for black utilities
• Support all design, installation, commissioning, qualification, training activities for black utilities
• Provide additional technical support to project team as required
• Adhere to all Quality & environmental regulations within area of responsibility
• Support technical development of Facilities Technicians after handover to LOB
• Continuous process improvement using cLEAN® concepts
• Maintain & establish standards for procedures & maintenance plans
• All safety & environmental requirements in the performance of duties

Facilities Engineer I/II - Wastewater Systems API

Analyst

• Provide subject matter expertise in Computer Systems Validation, process improvement, and IT compliance service delivery management across the site.
• Ensure that IT solutions are implemented and released to use in compliance with relevant regulations and standards facilitating the seamless transition and handover of projects to service operations with key stakeholders.
• Ensure governance and continuous improvement as an enabler supporting product quality, patient safety, and data integrity and contributes to the organization's goals of improving the lives of people with chronic diseases.
• Participate in all IT solutions validation activities including but not limited to: IT Infrastructure, IT Systems, and Computerized Equipment’s supporting Laboratories, Manufacturing, and Business Areas like Facilities and Warehousing.
• Ensure that IT solutions are compliant with relevant regulations and standards, e.g. 21 CFR Parts 11, EU Annex 11, and GAMP requirements among others.
• Facilitate, review, approve and as required develop validation deliverables including but not limited to URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ), Operating and Maintenance Instruction.
• Conduct risk assessments and impact analyses to identify potential compliance issues and develop mitigation strategies.
• Provide guidance and support to project teams on validation and qualification requirements.
• Continuously monitor and improve documentation and processes to ensure compliance with regulatory requirements and Novo Nordisk standards while working to identify efficiencies in the CSV program approach, applying lessons learned, and stay informed of industry regulatory changes as it applies to CSV.
• Perform assigned Quality Systems activities including Document Management system, Change Control, Deviations, and CAPA’s Writing and/or revising procedures applicable to CSV activities.
• Work in collaboration with the Engineering group to prepare the validation, requalification, and maintenance program.
• Facilitate the seamless transition and handover of projects to service operations with key stakeholders.
• Maintain system documentation and process according to Novo Nordisk standards and in compliance with regulatory requirements.
• Participate as a CSV SME in audits and inspections and provide needed documentation to demonstrate validated state and release to use.
• Collaborate with cross-functional teams to ensure that all IT solutions meet business needs, are delivered on time & within budget, and are properly documented and released to use.
• Ensure that all documentation and processes are following regulatory requirements and Novo Nordisk standards.
• Provide leadership and expertise in IT CSV, process improvement, and project coordination.
• Coach and mentor personnel, and provide guidance as needed.
• Participate in process group meetings and contribute to process group activities.
• Execute project activities and process improvement by incorporating cLEAN tools for visual management to track service delivery performance and communicate progress to stakeholders.
• Utilize problem solving skills to handle deviations to ensure they are properly documented, investigated, and resolved in a timely manner, as well as ensuring subsequent changes are properly documented, assessed for impact, and implemented in a controlled manner.
• Develop and deliver training programs for CSV and process improvement initiatives.
• Communicate effectively with stakeholders at various levels of the organization to ensure that CSV issues, improvement opportunities, and service delivery meet business needs and are aligned with regulatory requirements and Novo Nordisk standards.
• Moreover, will also perform other duties as assigned.
• Follow all safety & environmental requirements in the performance of duties.

Senior Computer Systems Validation Analyst

Compliance

• Provide subject matter expertise in IT compliance, process improvement and IT compliance service delivery management across the site
• Ensures that IT solutions are compliant with relevant regulations and standards and facilitates the seamless transition and handover of projects to service operations with key stakeholders
• Ensures governance and continuous improvement as an enabler supporting product quality, patient safety, and data integrity and contributes to the organization's goals of improving the lives of people with chronic diseases
• Develop and maintain validation and qualification documentation
• Conduct risk assessments and impact analyses to identify potential compliance issues and develop mitigation strategies
• Provide guidance and support to project teams on validation and qualification requirements
• Continuously monitor and improve documentation and processes to ensure compliance with regulatory requirements and Novo Nordisk standards
• Facilitate the seamless transition and handover of projects to service operations with key stakeholders
• Maintain system documentation and process according to Novo Nordisk standards and in compliance with regulatory requirements
• Participate as an IT SME in audits and inspections and provide needed documentation to demonstrate validated state and proper management of IT solutions throughout the life cycle
• Collaborate with cross-functional teams to ensure that all IT solutions meet business needs, are delivered on time & within budget, are properly documented, and managed throughout their life cycle
• Ensure that all IT solutions, documentation, and processes are following regulatory requirements and Novo Nordisk standards
• Provide leadership and expertise in IT compliance, process improvement, and project coordination
• Coach and mentor personnel, and provide guidance as needed
• Participate in process group meetings and contribute to process group activities
• Follow all safety & environmental requirements in the performance of duties

Senior IT Compliance Analyst

• Set strategic direction and lead the execution of comprehensive Total Rewards solutions
• Combine strategic insight, data-driven decision-making and strong stakeholder collaboration
• Lead a global team of 11 Total Rewards professionals supporting Europe (excluding HQ), Canada and Emerging Markets
• Use internal and external market data to design competitive, compliant and scalable reward solutions aligned with business strategy
• Partner with senior leaders, HRBPs and Total Rewards HQ teams
• Develop team capability through knowledge sharing, coaching and a strong focus on continuous improvement

Director, Global Total Rewards

Vice President

• Lead the Global Public Affairs department through transformation
• Set and drive the global public affairs strategy and priorities
• Establish governance for public affairs standards
• Serve as the escalation point for public affairs issues
• Represent Novo Nordisk as a trusted external leader
• Mentor and enable public affairs leaders across the organization

Vice President, Global Public Affairs

• Be accountable for and lead end-to-end regulatory submission activities for cross-product, cross-site, and manufacturing facility/equipment change projects.
• Contribute to new product submissions by leading regulatory strategies and activities related to manufacturing facilities and equipment.
• Coordinate activities related to the creation and maintenance of dossier documentation for manufacturing facilities, manufacturing equipment, and associated processes (such as cleaning validation, sterilisation, environmental monitoring, media-fill etc).
• Demonstrate strong leadership by setting the strategic regulatory direction for projects.
• Acting as an RA Site Partner by fostering close collaboration with manufacturing sites to proactively align on planned site-level changes.

Regulatory Affairs Specialist – RA Manufacturing Facilities, Projects

Mechanical Engineer

• Generating ideas and designing mechanical solutions for advanced aseptic production systems
• Creating 2D and 3D models using CAD software
• Testing and prototyping solutions, including hands-on work with 3D printing
• Contributing to solutions that are implemented in production sites around the world (Denmark, China, Brazil, France, and the US)
• Collaborating with academics, technicians and external development partners across different disciplines and countries

Mechanical Engineer Intern

• Support selected projects and products in the Novo Nordisk portfolio
• Provide strategic and scientific input to support development
• Secure regulatory approvals, and ensure compliance with evolving global regulations
• Lead and drive strategic regulatory device activities for drug-device combination products
• Plan, prepare, and lead health authority interactions and meetings
• Identify regulatory risks and opportunities, and provide clear recommendations

Regulatory Affairs Specialist – Device

• Formulate, Negotiate & Scale Strategic eHealth Partnerships: Commercial Integration Strategy: Actively shape and execute APAC’s direct-to-patient commercial strategy to achieve our regional volume through eHealth channels.
• Complex Deal Architecture: Lead end-to-end negotiation, customized commercial structuring, and deal closure with Tier 1 partners and digital disruptors.
• Portfolio Lifecycle Scaling: Design plug-and-play partnership frameworks to rapidly scale validated commercial models across growth markets.
• Cross-Functional Influence & Regional Network Governance: Serve as the primary regional connector across affiliates to align local general managers, business unit heads behind a shared digital roadmap.
• Data Infrastructure, Funnel Visibility & Optimization: Secure deep-tier API and data-sharing agreements with platform partners to stream certified analytics into our regional repository.
• Strategic GTM & Business Intelligence: Conduct market assessments to understand digital maturity, platform dynamics, and competitive behaviours across APAC.
• AI & Next-Gen Innovation Scouting: Evaluate emerging digital health trends to build defensible business cases and present investment recommendations to executive leadership.
• Commercial and financial modelling: Lead commercial and financial modelling to support digital and eHealth partnership strategy across APAC.