Novo Nordisk

QA Engineer

• Lead implementation and maintenance of assigned QMS processes (change control, deviations, CAPA, QRM), acting as local process owner and Veeva Vault superuser.
• Ensure ongoing compliance with corporate QMS and Czech regulatory requirements by monitoring obligations and driving corrective actions.
• Design, deliver and manage QMS training programs to ensure personnel competency and timely completion of required training.
• Support audit and inspection readiness, participate in internal audits and regulatory inspections, and coordinate quality management reviews.
• Develop and execute quality assurance strategies and KPIs to monitor, measure and continuously improve QMS performance.
• Perform risk assessments across the value chain (production, QC, storage, distribution), provide mitigation recommendations and ensure implementation.
• Represent QA in cross-organizational process groups, provide expert advice on complex quality issues, and drive change and process optimization with high independence.

Advanced QA Professional – QMS

Business Analyst

• Manage end-to-end O2C processes for multiple countries and contribute to process optimization and standardization.
• Hands-on support in SAP/S4 HANA SD for day-to-day operations and issue resolution.
• Identify root causes, design practical solutions and lead implementation across the O2C value chain.
• Drive month-end closing activities and enforce controls to maintain audit compliance.
• Coordinate with internal and external stakeholders including Finance, IT and Customers to ensure smooth operations.
• Deliver clear, timely communication and status updates to stakeholders and clients.
• Work independently to analyze data, prepare reports and recommend improvements.

Associate Business Analyst – Order to Cash

Operations

• Support in designing future-state processes and build implementation roadmaps
• Establish and maintain standardized, documented processes
• Drive operational excellence through proactive solutions, digital tools, automation, and AI
• Manage cross-functional projects in procurement and finance
• Lead change management initiatives
• Monitor performance metrics, mitigate risks, and implement continuous improvements

Manager – Operations Excellence – S2P

Manager

• Lead patient-centred, public health oriented market access strategies
• Develop and execute pricing and reimbursement plans
• Prepare value dossiers and submissions that clearly articulate patient benefit, system value, and public health impact
• Negotiate with payers to secure fair reimbursement and access pathways
• Engage key opinion leaders and medical associations to align strategies with patient and public health priorities
• Drive launch readiness by coordinating cross functional efforts
• Implement post launch lifecycle plans
• Lead price governance to ensure a sustainable product lifecycle and continued patient access
• Monitor policy, regulatory, and payer landscape changes
• Support advocacy and policy initiatives to help shape a sustainable, patient-centered access environment
• Implement and oversee price governance frameworks for company products

Senior Market Access Manager

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

Controller

• Finance Business Partner for CMRQ/GMO office
• BP Headcount planning and tracking
• Personnel related cost planning and monitoring
• Cost PBI report upgrading/CR/trouble shooting support
• Master data management
• Audit coordination

Business Controller

• QMS業務のレビュアーおよび承認者
• バッチ文書のレビューおよびリリースを担当する。
• 逸脱(Deviation)、変更申請/変更管理(Change Request)、および顧客苦情(Customer Complaint)に関する評価・承認を行う。
• 患者および製品に対する潜在的リスクを評価し、是正措置やリスク低減策を提案・実施する。
• 重大な影響が予想される事案はマネージャーや他部門と連携し決定する。
• 日常的な品質関連の意思決定を独立して行い、標準作業手順書 (SOP) 及び関連法規に基づき対応する。
• 重要事項や方針変更はマネージャーへエスカレーションする。
• 国内外の社内(品質、生産、ロジスティクス等)および外部規制当局と連携し、バリューチェーン全体のコンプライアンスと品質維持/向上を推進する。
• 医薬品製造におけるプロセス、設備およびユーティリティが、法規制および社内手順に適合していることを確認する。
• 事業部門(Line of Business:LoB)と連携し、高い品質意識の醸成を図る。
• 品質保証戦略の立案・実施を通じて、コンプライアンスと効率性の向上を推進する。
• リスク評価ツールによる予防的リスク管理を実践し、患者・製品リスクの低減を図る。
• データに基づく品質改善施策を導入し、継続的改善活動を主導する。
• 製造、技術、品質など関連部署と連携して、工場コンプライアンスのための新規手法を導入・実装する。

QA Professional

Account Manager

• Ensures consistent and thorough management of Employee Relations processes, including performance management.
• Leverages advanced business and industry knowledge to make process enhancements.
• Leads, participates, and performs Employee Relations and Corrective Action processes.
• Counsels and provides assistance to employees and various levels of management in employee or management issues guided by company’s employee relations policies.
• Independently identifies and resolves complex problems, displaying a high level of critical thinking skills.
• Develops and maintains open and positive communication with all internal stakeholders and collaborative partners to assist in attaining departmental and company goals.
• Consistently promotes the fair and equitable treatment of employees involved in Employee Relations related processes.

Senior Employee Relations Manager

Product Specialist

• Identify and map key stakeholders within the assigned region to implement marketing initiatives
• Engage regularly with doctors to promote products, address queries, and secure prescriptions
• Meet sales effectiveness KPIs by achieving call averages and related targets
• Ensure timely supply and availability of products by liaising with agents and placing orders
• Conduct ongoing prescription audits and competitive analysis to track doctor engagement
• Support strategic segmentation of doctors and provide market feedback to sales leadership
• Collaborate with internal teams and maintain disciplined reporting and administrative processes

Product Specialist / Senior Product Specialist

General Counsel

• Support Legal & Compliance Reviews – Assist on the ethics navigator with Novo Nordisk corporate requirements.
• Business Ethics Oversight – Collaborate with lawyers on ethics matters, review third-party documentation, identify risks, and recommend mitigation strategies.
• Drive Compliance Initiatives – Manage and update projects like TEN (The Ethics Navigator) and HIRO, ensuring alignment with local regulatory requirements.
• Enable Product Launch Compliance – Support the Business Ethics Compliance Programme and related legal activities for new product introductions.
• Data & Reporting Management – Track and report compliance data using tools like COUPA and Privacy Management systems; maintain trackers, reports, presentations, and training materials.

Associate Legal Counsel

• Identify and map key stakeholders within the assigned region to implement company marketing initiatives, working closely with the Area Sales Manager.
• Engage regularly with doctors to promote company products, address queries, overcome objections, and secure prescriptions.
• Meet sales effectiveness KPIs by achieving required call averages, frequency, coverage, personal order bookings, and related targets.
• Ensure timely supply and availability of products by liaising with C&FA agents and stockists and placing necessary orders.
• Conduct ongoing prescription audits and competitive analysis to track doctor engagement, evaluate previous visit outcomes, and monitor competitor activity.
• Support strategic segmentation of doctors, assist in order booking, and provide feedback on market developments to sales leadership.
• Collaborate with internal teams, organise approved educational activities, and maintain disciplined, timely reporting and administrative processes.

Product Specialist, Senior

Marketing

• Support the development & execution of local portfolio marketing strategy along with the Senior Marketing Manager
• Actively launch campaigns & sales execution to achieve short and long-term business objectives
• Analyze, understand, and interpret market insights and translate to simple & targeted communication
• Proactive development of marketing/promotional mix to meet brand objectives and customer needs
• Utilize multi-channel tools to communicate key brand messages to market
• Prepare annual/cyclic action/brand plans to meet business objectives
• Design innovative marketing campaigns that help sales team meet business objectives
• Liaison with external agencies to deliver initiatives for brands and maintain constant touch with internal and external customers
• Launch new products in line with local strategy and regional approval.

Marketing Manager, Insulin

• Develop and execute a comprehensive strategic plan for the launch of a rare disease product in the specialty segment
• Collaborate with cross-functional teams to ensure alignment and successful execution of launch strategies
• Conduct thorough market research to understand unmet needs and healthcare provider dynamics within the specific rare disease specialty segment
• Lead and oversee multiple projects aimed at therapy shaping within the rare disease space
• Build and maintain strong relationships with key opinion leaders and healthcare professionals to gather insights and foster support for the upcoming product launch
• Establish key performance indicators (KPIs) and regularly evaluate the success of launch strategies
• Manage branding for Rare Disease, Obesity, and Diabetes within the managed care business

Marketing Manager

Medical Reviewer

• Conducting medical reviews of clinical trial data to ensure patient safety, protocol compliance, and adherence to regulatory requirements
• Collaborating closely with study group members, including Data Managers, Trial Managers, and Medical Specialists
• Identifying and resolving issues of medical concern and inconsistencies in clinical trial data
• Presenting findings of medical reviews to relevant Medical Specialists
• Documenting medical reviews in the sponsor Trial Master File (TMF)
• Performing quality control of medical review tasks and findings
• Providing training and mentoring to new team members
• Contributing to shared best practices, process improvements, and other activities
• Planning and managing resources for medical review tasks

Senior Medical Reviewer

• Perform Medical Review of all trial subjects of assigned clinical trials
• Ensure patient safety and adherence to protocols, GCP, ICH Guidelines
• Collaborate with study group members during trial conduct
• Report status of medical review to project as appropriate
• Consult with Trial Managers and Medical Specialists
• Contribute to trial planning activities related to medical review
• Resolve issues of medical concern in clinical trial data
• Document medical review in the sponsor TMF
• Review and provide inputs to medical monitoring displays