Novo Nordisk

Consultant

• 传达公司产品的医学信息
• 执行产品的推广策略
• 及时提供相关产品的市场信息
• 向客户提供专业和良好的服务,保持公司形象

Senior Medical Consultant

Project Manager

• Drive risk reporting, strategic projects, and ad hoc tasks for the North American Finance Organization
• Manage the Enterprise Risk Reporting Process on behalf of NNI, which includes quarterly updates and submissions to HQ
• Lead semi-annual risk workshops with leaders from across the organization
• Structure an updated, more comprehensive Risk Profile approach
• Update current risk reporting in line with information gathered
• Perform quantitative analysis to assess risks
• Collaborate with Director of team and Global Risk Office as well as NNI ET on finalizing risk picture
• Independently manage and execute projects working closely together with respective F&SC LT members
• Communicate around strategic finance initiatives to the F&SC organization

Senior Risk & Project Manager

Financial Planning and Analysis

• Supporting the Finance & Investment Manager with strategic finance projects, including data analysis, tracking project progress, and preparing presentations.
• Performing data analysis and supporting the preparation of financial reports.
• Supporting the development and maintenance of reporting and analysis tools.
• Developing and maintaining team SharePoint sites.
• Supporting team meetings and team day planning to help maintain a positive and engaging team atmosphere.

Finance Intern

Product Marketing

• Support daily activities of Warehouse and GMP team
• Contributing to and executing improvement initiatives in warehouse and GMP processes
• Preparing, updating, and optimizing Value Stream Mapping and other process visualizations
• Supporting workflows, document processes, and operational needs in daily operations
• Helping identify and drive process optimizations
• Coordinating and assisting with minor IT-related tasks and system support

Intern, Warehouse Support – GMP Team

Research Scientist

• Lead toxicopathology excellence across exploratory, nonclinical, and GLP studies.
• Act as Sponsor's Peer Reviewing Pathologist (PRP), evaluating toxicopathology findings, the pathology report and overseeing the quality and credibility of pathology data across internal and Contract Research Organization studies (both GLP and non-GLP).
• Lead pathology data responsibility across assigned projects, including evaluation, interpretation, and safety assessment for both study reports and regulatory submissions to health authorities.
• Develop and advance toxicopathology methods and practices, ensuring optimal techniques, up-to-date terminology, and diagnoses applied across projects and the broader organization.
• Mentor and supervise peers and junior colleagues, fostering scientific excellence and knowledge-sharing within the discipline.
• Bridge toxicology and pathology expertise across project teams, presenting scientific findings at design reviews, safety committees, and departmental meetings.
• Help advance digital pathology capabilities.
• Prepare regulatory documents and lead interactions with health authorities on pathology and safety matters.
• Participate in due diligence activities, evaluating nonclinical pathology and toxicology data to inform business decisions.

Senior Principal Scientist, Toxicopathology

Business Analyst

• Manage IT system operations, maintenance, and development
• Independently configure SuccessFactors Employee Central
• Ensure compliance with regulatory and organisational standards
• Collaborate with stakeholders to align IT systems with business needs
• Oversee vendor management and service delivery
• Drive innovative ITIL-based change and release management processes

Advanced Business Analyst I – SuccessFactors, EC

Manager

• Own the end-to-end process of developing, negotiating, and executing Clinical Trial Agreements and budgets.
• Be the bridge between clinical teams, legal, finance, and our clinical trial sites ensuring everything runs smoothly while maintaining compliance and quality.
• Negotiate and draft contracts and Master Services Agreements with clinical sites and vendors in coordination with legal and compliance teams.
• Prepare and negotiate investigator and trial budgets directly with clinical sites, ensuring alignment with local Fair Market Value and global requirements.
• Manage commercial and contractual relationships with investigators, clinical sites, and key internal stakeholders to meet clinical trial timelines.
• Identify cost-saving opportunities and implement strategies to enhance cost efficiency across trial budgets.
• Oversee the signing, shipping, and repository management of contractual documents in electronic systems.
• Evaluate protocol changes for budget impact, negotiate amendments, and escalate financial issues when needed.
• Support high-quality execution of clinical trial contract and budget activities in compliance with ICH-GCP and regulatory requirements.

Contract and Budget Manager

Clinical Research

• Leading data-driven feasibility assessments at country and site level
• Contributing scientific and strategic insights to the Trial Portfolio Review process
• Expanding the site network by developing strong partnerships with new sites and Key Opinion Leaders
• Acting as the main point of contact for feasibility-related queries
• Defining and validating study assumptions, developing country and site strategies
• Maintaining up-to-date knowledge of competitor trials and regulatory landscapes
• Ensuring high-quality execution of feasibility activities in compliance with ICH-GCP

Feasibility Manager

Engineer

• Lead the development of life-saving packaging systems where technical expertise meets project leadership—and your work protects both product quality and patient safety.
• Take on a unique hybrid role that combines hands-on technical development of primary packaging with coordination and project leadership responsibilities.
• Develop robust, compliant packaging systems for parenteral administration while driving cross-functional projects from concept through to delivery.
• Develop primary packaging systems and components (e.g., vials) including specifications, drawings and test documentation that meet regulatory and industry requirements.
• Take ownership for planning and coordinating project execution: setting clear goals, managing timelines, resources and budgets, and monitoring progress to meet scope, quality, schedule and cost targets.
• Lead and engage cross-functional project teams, fostering a committed project culture and ensuring effective governance is in place.
• Contribute to safety risk management, requirement engineering and medical device development activities.
• Coordinate and collaborate with external suppliers and manufacturers throughout development and transfer activities.
• Drive change requests, troubleshoot technical issues and participate in systematic problem-solving across development activities.
• Report project performance to stakeholders and perform integrated change control while ensuring compliance with Novo Nordisk Quality Management System.

Product Development Engineer

Procurement

• Lead high-visibility negotiations with senior stakeholders
• Structure complex business models and agreements
• Support development of innovative pricing models
• Provide daily support on contract strategy

Associate Contract Director, CMC Outsourcing

QA Automation Engineer

• Ensure new processes & equipment are compliant with line of business and global standards.
• Participate in local & global team to ensure new equipment & processes are designed to meet URS & IFA designed by Novo Nordisk ensuring the equipment will be ready for install & qualification as well as successful ramp up of equipment.
• Improve reliability of the process control systems to meet current & projected customer, business & regulatory requirements through focus on people & equipment, as well as serving as gatekeeper for standards.
• Work with local & global project team to ensure design of process is compliant with local & global standards
• Develop interface agreements & align requirements with equipment vendors
• Develop & implement plans to maintain & improve process control systems
• Schedule & execute plans in coordination with manufacturing schedules
• Assist with developing & managing expense budgets for maintaining & improving process control systems
• Develop & maintain automation standards, specifications & maintenance plans
• Own self development & initiative to understand the site process control systems
• Support audits & inspections as SME for process control systems
• Coach & train colleagues & stakeholders in relevant areas
• Utilize the appropriate cLEAN® tools within the main areas of Systematic Problem Solving, process improvement, & project management
• Operate within compliance with a quality mindset that focuses on risk management & mitigation
• Implement effective change management
• Support Corporate, PS, local IT, & local stakeholder initiatives & projects
• Participate in the development of new SOPs, best practices, and maintenance procedures
• Follow all safety & environmental requirements in the performance of duties

Automation Engineer II – Automation, OT, API Production

• Collaborate with business stakeholders, project teams and vendors to ensure process control systems for new and existing equipment meet local and global standards
• Work with equipment suppliers and Schneider to specify field instrument assemblies and sensors, ensuring devices can connect to and be used in local manufacturing while meeting requirements from both people and equipment perspectives
• Act as a gatekeeper for standards
• Partnering with other departments such as QC and Warehouse, gather requirements (for example sensor temperature ranges) to guide equipment selection
• Execute qualification activities for FMS/BMS systems in GMP areas, participate in protocol development and execute qualification protocols as required
• Support periodic system evaluations, change requests and deviation handling that are critical to maintaining our license to operate
• As an expert on FMS/BMS software interfaces, configure alarms and reports and provide training and guidance to others
• Responsible for one or more HVAC and FMS/BMS equipment items, working closely with maintenance and production to plan, coordinate and release facility activities

Associate Automation Engineer – HVAC, FMS/BMS

• Lead market access and value activities for Novo Nordisk’s Rare Disease portfolio in the North UK
• Design and implement value-driven access strategies
• Develop tools and services that address NHS needs
• Secure formulary and pathway adoption to improve patient outcomes
• Develop and deliver market access campaigns, tools and services
• Lead Advanced Budget Notification and pathway development for new rare disease products
• Manage local formulary positioning, guideline development and implementation of local contracts and population health solutions
• Create and execute strategic partnerships and projects that support NHS service delivery and address health inequalities
• Deliver strategic account management at system/ICS level and lead payer advocacy and advisory boards
• Collaborate with marketing, medical, HEOR (Health Economics and Outcomes Research), pricing, Legal & Compliance, and field teams to develop compliant materials
• Maintain and update customer databases and manage Promomats processes
• Monitor and evaluate the effectiveness of access strategies and provide feedback for continuous improvement

National Market Access Manager

Attorney

• Monitor and interpret relevant laws, regulations and standards to ensure the cluster operates within legal frameworks
• Provide legal advice on contracts, corporate matters and commercial operations; draft, review and negotiate legal documents
• Design, implement and maintain compliance policies, procedures and training to promote a strong culture of compliance
• Support risk identification, assessment and mitigation activities, including investigations via the Compliance Hotline
• Collaborate with internal teams, external counsel and regulators; act as the key point of contact for legal and compliance matters in the cluster
• Represent the cluster in legal/compliance networks and coordinate roll-out of HQ initiatives in alignment with Clusters Associate Director
• Drive continuous improvement of legal and compliance processes, tools and reporting

Legal, Ethics & Compliance Manager

Executive Assistant

• Performs a wide range of highly diverse and complex assignments of a responsible and confidential nature for a VP, CVP, or SVP requiring a high level of tact, discretion, persuasion and/or negotiation.
• Monitors access and redirects correspondence on behalf of the executive based on priorities he/she sets.
• Directly supports a VP, CVP, or SVP.
• Interacts with internal and external sources at the executive level requiring skill, tact, influence and/or negotiation.
• Interacts with global HQ and affiliates on matters of importance.
• Provides direction/coordination of workflow to lower level clerical/administrative positions.
• Participates on the leadership team of the function he/she supports and may be a participant on the ET Admin Council if position reports to an ET Member.
• Collaborates closely with other administrators, business leaders and global colleagues.
• Coordinates and executes output and actions from the leadership team meetings.
• Designs, plans, and executes moderate to large scale meetings and off-sites.
• Directs administrative activities, develops and organizes procedures, and uses considerable written and verbal communication skills to represent the department.
• Ensures company procedures are followed and directs questions accordingly.
• Functions autonomously, exercises discretion and judgment, and works independently on a variety of complex and diversified assignment and special projects.
• Handles correspondence and requests for information and may make decisions on behalf of the executive.
• Independently researches and develops reports and budgets; draws conclusions and makes recommendations.
• May lead moderately complex projects within own department or that have a cross functional nature.
• May provide support for budgets.
• Participates in planning and other business related meetings.
• Performs a wide range of administrative and general support duties of a highly responsible and confidential nature.
• Performs duties that are both task and project oriented requiring interpretation and judgment.
• Performs other clerical/administrative and support duties as needed.
• Plans and prepares communications requiring skill, tact, persuasion, and/or negotiation to accomplish the objectives of the communication.
• Provides support to team members for general administrative needs such as presentation development, greeting guests, and new hire onboarding.
• Typically performs a variety of routine office duties involving typing, invoicing, record and file maintenance, data entry, meeting/travel arrangements, planning and execution of either on or offsite department meetings, processing expense reports, department event planning (e.g. off sites, team building, group meetings), running reports, vendor management etc.