Jobs at Sandoz

Manages global regulatory submission projects and supports regulatory strategy, intelligence, systems, and processes for biosimilar and generic medicines. Maintains documentation standards, records retention, regulatory compliance, and submission dossiers. Collaborates with internal and external stakeholders, analyzes data, supports technical projects, and reports product complaints, adverse events, and special cases within required timelines.

The Technology Workstream Lead drives technology integration and implementation for the Sandoz STEP Transformation Program, ensuring alignment with business goals and managing project deliverables.

Lead and oversee global/regional pharmacovigilance operations for post-marketing and clinical trials. Ensure regulatory-compliant adverse event intake, processing, reporting, signal detection, CAPA execution, inspection readiness, audits, and cross-functional stakeholder coordination. Build and manage high-performing safety teams, recruit and develop talent, track KPIs, and optimize operational efficiency for timely safety reporting and clinical trial support.

Lead global technology operations for manufacturing and engineering solutions: own service delivery, lifecycle management, SLAs, governance, vendor management, incident management, budget accountability, and ensure GxP/ITIL/CSV compliance while driving digital manufacturing strategy and cross-functional integration.

Manage strategic relationships with key pharmacy and wholesale accounts to drive sales, profitability, and market share. Develop account plans, lead negotiations and listings, analyze sales and market data, and coordinate cross-functional teams to execute customer strategies and improve forecasting.

Supports US Biosimilar Regulatory Affairs by executing regulatory strategies, preparing eCTD submissions, managing regulatory documents and archives, tracking activities, coordinating health authority interactions, maintaining compliance materials, and supporting product launches and lifecycle management. The role collaborates with global and cross-functional teams to ensure timely submissions, approvals, and post-marketing regulatory compliance for biosimilar products.

Develops and maintains global product labeling strategies for biosimilar and generic medicines. Reviews country labels, assesses deviations from core labeling, supports safety communications and portfolio stewardship, prepares regulatory documents and responses to health authority queries, and contributes to labeling negotiations. The role also monitors labeling processes, systems, quality, and compliance while collaborating with internal and external stakeholders across regions.

Manage pharmacy accounts and territory strategy for generics: identify and prioritize customers, achieve sales and performance targets, negotiate commercially, design marketing and training initiatives, collect market/competitor intelligence, deliver reports, and ensure customer satisfaction and compliance with company policies.

Field-based role managing pharmacy accounts and territory strategy to drive sales of generic medicines. Responsibilities include client segmentation, negotiation, marketing and training, reporting market intelligence, delivering campaigns, ensuring compliance, and meeting sales and coverage targets.

Leads strategic pricing, contracting, and financial analyses supporting market access and customer decisions across pharmaceutical channels. Owns business case development, financial modeling, scenario analysis, profitability evaluation, governance, and leadership recommendations. Partners cross-functionally with Market Access, Brand, Finance, Contracts, Sales, and Analytics teams. Develops dashboards and reporting, monitors deal performance, drives process improvements, mentors team members, and supports data-driven commercial decision-making.

Field-based role managing pharmacy accounts and chains within an assigned territory. Responsibilities include sales target attainment, negotiation, marketing and training initiatives, customer relationship management, market intelligence gathering, reporting, and promoting generics adoption while ensuring compliance with company policies.

Supports finance strategy through financial reporting, forecasting, budgeting, accounting, tax reporting, audit support, and management analysis. Oversees actuals and forecast processes, ensures financial data and reporting-system integrity, automates routine reporting from SAP and BW, and serves as a Finance and Controlling super user. Supervises and develops a small team while driving process optimization, stakeholder engagement, compliance, and timely delivery of accurate financial information.

Provide analytical support for financial reporting, compliance, and data accuracy. Prepare and deliver timely reports and analyses, maintain fixed asset register and assist general ledger tasks. Support finance projects, produce written proposals and presentations, and report technical complaints/adverse events promptly. Collaborate with managers and senior colleagues to ensure accurate, compliant financial information and internal customer satisfaction.

Manage and optimize P&O services for the Iberia client group: implement global P&O processes, coordinate service delivery, drive continuous improvement, support budgeting and SLAs, lead a small team, and ensure timely reporting of product-related adverse events.

Act as primary on-site contact for IT infrastructure at Holzkirchen: run local infrastructure projects, maintain LAN, data center, desktops and printers, coordinate vendors, ensure compliance, report KPIs, drive service improvements, perform RCA and incident resolution, and escalate product-related technical complaints within 24 hours.

Lead a marketing team to define and execute brand and portfolio strategies for biosimilars and hospital generics. Drive forecasting, budgeting, resource allocation, market intelligence, promotional mix, and cross‑functional stakeholder engagement to maximize commercial value and growth.

Perform GxP monitoring and QA investigations, implement and maintain local quality systems and SOPs, ensure cGMP/GDP compliance for handling and distribution, manage change control, complaints, recalls and product inspections, support product launches, liaise with regulators and partners, and report adverse events promptly.

Lead creation and implementation of a global pre-launch forecasting capability for generics, biosimilars, and specialty assets. Build and manage a cross-functional team, embed forecasting frameworks and governance, integrate advanced analytics and AI/ML, deliver scenario-based forecasts, and drive adoption and alignment with commercial stakeholders to inform portfolio and launch decisions.

Leads the global Unified Endpoint Management service portfolio, including strategy, governance, endpoint engineering, mobility, application packaging, virtual workplace services, digital employee experience, security compliance, operations, vendors, budgets, and globally distributed teams. Owns service roadmaps, performance metrics, risk remediation, lifecycle management, automation, and continuous improvement while partnering with cybersecurity, infrastructure, architecture, procurement, stakeholders, and strategic suppliers.

Support planning, execution, and optimization of marketing strategies for generics and biosimilar medicines in Australia. Coordinate campaigns, launches, patient support programs, events, and reporting while collaborating with sales, regulatory, and medical affairs to ensure compliant, effective marketing.