Jobs at Sandoz

Provides upstream bioprocess subject-matter expertise across biologics manufacturing, technology transfer, process lifecycle management, validation, investigations, and continuous improvement. Supports fed-batch, intensified fed-batch, and continuous perfusion processes; evaluates emerging technologies; resolves deviations and implements CAPAs; manages CPV, APR/PQR, change controls, scale-up, process characterization, and PPQ documentation across internal sites and external manufacturing partners.

Leads the global upstream Manufacturing Science and Technology Center of Excellence for commercial biologics. Oversees technology transfers, process lifecycle management, manufacturing and validation support, technical investigations, continuous process verification, regulatory readiness, innovation adoption, and process improvement across internal sites and external manufacturing partners. Provides scientific governance for upstream processes, drives analytics and automation initiatives, and develops technical leaders and succession capabilities.

Leads end-to-end strategic sourcing of active pharmaceutical ingredients for Sandoz development projects, from early evaluation through registration and launch handover. Responsibilities include sourcing strategy, global supplier identification, technical and commercial due diligence, negotiations, contracting, supplier performance management, risk mitigation, compliance, and cross-functional project coordination. The role ensures API quality, availability, cost effectiveness, regulatory readiness, and supply resilience across international development programs.

Leads the Biopharma and Hospital business unit, including portfolio strategy, product launches, sales and marketing performance, P&L, budgets, market access, competitive analysis, stakeholder engagement, compliance, and team development. The role drives regional and country-level commercial strategy, maximizes revenue and profitability, develops high-performing teams, and coordinates cross-functional brand and launch planning across global, regional, and local markets.

Leads pharmaceutical sales operations and a team of Key Expert Specialists to achieve sales, productivity, performance, and development targets. Develops business plans, manages budgets and resources, coaches and develops staff, supports strategic brand planning, builds customer and key account relationships, gathers market intelligence, and ensures compliance, reporting, customer satisfaction, and adverse-event reporting. Requires strong specialty pharma knowledge, particularly oncology, biologics, or biosimilars.

Leads financial planning and analysis for Sandoz Regulatory Affairs, supporting an approximately $80 million budget and 700 FTEs across global locations. Acts as a strategic finance partner to leadership, managing reporting, forecasting, budgeting, cost monitoring, savings initiatives, and financial governance. Drives transformation, project tracking, ROIC modeling, process standardization, and automation while guiding cross-functional teams and ensuring forecasting accuracy, budget compliance, and effective financial decision-making.

Manage Irish marketing authorisation applications and lifecycle activities for generic and biosimilar medicines. Prepare submissions, variations, renewals, transfers, risk management plans, and educational materials; ensure compliance with EU, HPRA, and Sandoz requirements. Respond to HPRA queries, monitor regulatory changes, support audits and inspections, manage CAPAs and deviations, update procedures, and coordinate with internal, EU, local, and external stakeholders.

Prepare, validate, dispatch, and submit compliant regulatory filing packages according to health authority requirements and submission timelines. Maintain eCTD lifecycles, regulatory information management databases, and document systems. Support document preparation, quality checks, uploads, audits, issue escalation, and coordination with global regulatory teams and country organizations. The role requires strong organization, communication, compliance awareness, adaptability to IT tools, and the ability to work independently in an international environment.

Manage pharmaceutical regulatory registrations, product information, translations, packaging artworks, regulatory databases, and compliance documentation. Coordinate with health authorities and internal stakeholders to support approvals, audits, inspections, product launches, and manufacturing site transfers. The role requires strong planning, attention to detail, communication skills, Dutch and English fluency, and experience working in a regulated pharmaceutical environment.

Lead and report complex, risk-based GMP audits across pharmaceutical and medical device operations, including manufacturing sites, laboratories, suppliers, and quality systems. Evaluate compliance, audit findings, and CAPA plans; provide regulatory guidance; escalate critical issues; advise business units; and support remediation, training, continuous improvement, and quality-system best practices. Mentor junior auditors and maintain expertise in applicable regulations and standards. The role requires strong leadership, independent judgment, and approximately 60% travel.

Manage strategic healthcare and pharmaceutical accounts in Italy, driving sales growth, customer development, commercial strategy, negotiations, and performance targets. Build relationships with key stakeholders, analyze market and competitors, coordinate customer events, maintain CRM data, and support marketing and medical initiatives. The role also includes sales operations planning, team training or coaching, adverse-event reporting, sample distribution, and field-force activities.

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.

Develop product and brand strategies for biosimilar medicines, create promotional campaigns and integrated commercial plans, conduct market research, and monitor market and product performance. Lead cross-functional brand teams, manage marketing budgets and forecasts, ensure compliant promotional execution, and evaluate marketing effectiveness. The role requires pharmaceutical or healthcare experience, fluent Italian and English, and strong collaboration, negotiation, and stakeholder-management skills.

Leads governance, strategic planning, execution, performance management, and executive decision-making for Sandoz’s global business and technology transformation program. The role coordinates cross-functional workstreams, implementation partners, risks, dependencies, milestones, quality, and commercial changes. It facilitates governance forums, maintains program reporting and records, drives accountability, supports deployment readiness, and improves transformation delivery processes. The position requires strong analytical, communication, stakeholder-management, and program-governance capabilities in complex global organizations.

Manages pharmacy accounts, chains, and groups across an assigned territory. Responsibilities include customer segmentation, sales and performance objectives, budget management, commercial negotiations, marketing campaigns, pharmacist training, relationship building, and territory optimization. The role also gathers market intelligence, analyzes competitor activity, and collaborates with internal teams to improve business effectiveness while complying with regulatory requirements and company procedures.

Supports sales representatives, channel partners, pharmacies, and customers by managing orders, returns, stock analysis, product inquiries, reporting, and issue resolution. Provides personalized customer care, coordinates pharmacy value proposition implementation, monitors sales-force consultations, and identifies process improvements. Collaborates with sales, customer care, and marketing stakeholders while maintaining order-management compliance and financial controls.

Leads a district pharmaceutical sales team, owns revenue and productivity targets, develops business and brand plans, manages budgets and resources, coaches medical representatives, maintains key account relationships, monitors market and competitor intelligence, and ensures compliance, reporting, customer satisfaction, and product safety processes.

Provide dedicated executive support to the SVPs of North America Strategy & Growth and General Counsel. Responsibilities include complex calendar management, meeting prioritization, travel logistics, confidential stakeholder communication, leadership meeting coordination, legal and compliance support, strategic planning activities, executive reviews, off-sites, and cross-functional initiatives. The role also improves administrative processes and collaboration while exercising sound judgment, discretion, and proactive follow-through in a hybrid Princeton, New Jersey headquarters setting.

Leads end-to-end delivery of complex SAP projects across transformation, regulatory, lifecycle, BAU, and M&A portfolios. Manages scope, schedules, budgets, risks, dependencies, vendors, governance, quality, and stakeholder engagement from initiation through operational transition. Oversees cross-functional and external teams, financial and commercial controls, executive reporting, compliance, security, testing, cutover, adoption, and benefits realization. Ensures delivery follows SAP CoE standards, clean-core principles, architecture guardrails, and regulated enterprise practices.

Supports supply planning and execution by maintaining accurate planning data, coordinating supply-demand balancing and order management, monitoring fulfillment and operational KPIs, escalating risks, and maintaining planning system data. Coordinates with demand planning, logistics, and manufacturing stakeholders to support planning cycles, resolve discrepancies, identify recurring issues, and ensure timely communication and execution.