Jobs at Novartis

The Manufacturing Specialist will lead investigation and corrective action processes for production deviations, apply root cause analysis, and ensure adherence to GMP standards while generating manufacturing orders and delivering training.

Field-based territory sales role supporting dermatology accounts. Build strategic territory plans, engage HCPs omni-channel, resolve access issues, coordinate cross-functionally, and deliver customer and patient support with frequent travel.

Serve as front-line recruiter for DACH (German) high-volume hiring: screen, shortlist, coordinate interviews, conduct first-round interviews, extend offers for junior roles, maintain Workday, and partner with Recruitment Business Partners to ensure a fast, compliant, and positive candidate experience.

Lead operational interface with external analytical service providers for outsourced analytical activities. Drive planning, forecasting, financial management, partner governance, capacity monitoring, risk mitigation, and continuous improvement while ensuring compliance with quality standards and close collaboration with internal stakeholders and global CROs.

Field-based immunology sales role responsible for meeting territory sales and market-share targets by building trusted HCP relationships, executing brand plans, using CRM and data to prioritize accounts, sharing market insights, and collaborating cross-functionally while maintaining compliance and ethical standards.

Lead development and execution of market access and payer strategies for neuroscience assets across the product lifecycle. Align HEOR, pricing, regulatory and commercial teams to secure reimbursement, shape evidence generation (RWE/HEOR), support country negotiations, manage budgets and access community, and deliver access materials to maximize patient access and market availability.

The Regulatory Affairs Manager ensures regulatory compliance, manages registration submissions and approvals, coordinates product availability, and maintains relationships with local authorities.

Author and oversee high-quality scientific publications and presentation materials across therapeutic areas. Provide QC, ensure compliance with SOPs and GPP, mentor team members, support publication strategy, and translate complex science into clear communications.

Manage end-to-end supplier/vendor quality activities including drafting QA agreements and annual monitoring reports, handling supplier change notifications, supplier qualification, QRA, audit and CAPA support, regulatory statement preparation, and coordination with SIM/TPRM and stakeholders for supplier quality deliverables.

Lead generation of integrated commercial insights by combining market research, analytics, and competitive intelligence to inform brand strategy, forecasting, and access decisions. Build and manage an insights team, align KPIs and dashboards with cross-functional stakeholders, and drive market modelling, scenario planning, and knowledge management to support commercial performance.

Lead and optimize country-level supply chain operations including customs, planning, warehousing, distribution, launches, and 3PL management. Drive continuous improvement, cross-functional alignment, talent development, and budget control to ensure supply continuity and adherence to global Novartis standards.

Lead the International Finance Center of Excellence to provide FP&A, strategic business partnering, resource allocation, and analytics capabilities. Drive budgeting, forecasting, KPI reporting, investment governance, automation and GenAI-enabled digital finance initiatives. Build and coach a global finance team, standardize processes, deliver self-service reporting, and partner with cross-functional stakeholders to support strategy execution and improve financial decision-making.

Lead enterprise data governance by defining frameworks, quality rules, and validation logic. Engage source teams to embed governance upstream, collaborate with stewards and owners on metadata, lineage, and compliance, deliver automation to optimize data lifecycle, and advise senior stakeholders to drive data-driven commercial outcomes and improved data maturity.

Drive neuroscience pharmaceutical sales in Kaohsiung by building long-term HCP and KOL relationships, executing key account strategies, using data to prioritize high-potential customers, delivering value-based engagements (in-person and virtual), personalizing multichannel outreach, translating feedback into action, and collaborating cross-functionally to align regional execution with national strategy.

Manage and govern customer and finance master data in SAP, support onboarding and training, drive process improvements, participate in UAT and projects, monitor data quality and KPIs, and support SOX compliance and audit readiness.

Perform and document analytical and microbiological testing on products, materials, and stability samples per GxP/GMP. Manage sample traceability, maintain compliant QC laboratory operations, report deviations or complaints promptly, follow radiation and safety regulations, and support continuous quality improvement in a radiopharmaceutical manufacturing environment.

The Technical Transfer Lead manages technical transfers in pharmaceutical manufacturing, leading project teams, ensuring compliance with guidelines, and developing technical strategies.

The Planning Lead will develop and implement procurement strategies, manage projects, maintain KPI tracking, and support stakeholder communication and operational excellence initiatives.

Lead global labelling for neuroscience products across lifecycle: develop and maintain core and market labelling, translate clinical and safety data into compliant content, drive cross-functional alignment, support health authority interactions, and implement approved labelling changes ensuring global consistency and traceability.

Lead the development of global labelling strategies for innovative medicines, ensuring compliance with regulatory requirements and alignment with product strategy, collaborating with cross-functional teams.