Jobs at Novartis

Lead design, training, and production deployment of advanced ML models (including deep learning and graph architectures) for drug discovery. Own end-to-end model lifecycle, build scalable inference services and automated MLOps pipelines, validate models against scientific benchmarks, optimize for performance, and mentor teams to raise engineering excellence.

Lead and grow a team of internal and external AI engineers to design, deploy, monitor, and operate production-grade AI agents and models for biomedical research. Ensure MLOps/AgentOps best practices, enterprise architecture alignment, security, compliance, and AI governance while delivering scalable, cost‑optimized, high‑quality solutions that integrate into applications and workflows.

Lead site quality operations and compliance with cGMP/GxP. Oversee validation (IQ/OQ/PQ), investigations, CAPA effectiveness, QA/QC support, KPI reporting, audits/inspections, and team development.

The Product Expert oversees product knowledge in the commercial lifecycle, ensures process validation, conducts data analysis, and leads improvement projects.

The Associate Director will oversee clinical quality assurance for trials, ensuring compliance with health authority standards and patient safety. Responsibilities include quality risk management, oversight of clinical processes, and collaboration with stakeholders to support audits and inspections and sustain quality improvements.

Manage key tasks for projects in Biologic drug development including documentation, approvals, and troubleshooting. Ensure compliance with GMP standards.

The Senior Brand Manager defines product strategy and implements tactical plans to ensure brand growth, monitors budgets, and collaborates with internal teams while reporting technical issues related to products.

The role involves managing strategic accounts, resolving challenges, and driving product demand to improve patient outcomes in the dermatology sector.

The DAM Librarian manages digital asset operations, ensuring quality, rights management, and curation while supporting onboarding and testing of new features.

The Process Engineer manages CAPEX projects for production equipment, develops business cases, oversees equipment procurement and commissioning, and ensures successful project execution within budget and timelines.

The role involves designing, executing, and analyzing experiments related to oligonucleotides, using advanced analytical methods. The candidate will provide mentorship, ensure compliance with regulations, and lead project activities.

The Associate Director will oversee quality assurance for clinical trials, ensuring compliance with health authority requirements and internal standards while providing guidance on Good Clinical Practice and managing quality risks.

The Territory Account Specialist leads account management, builds relationships with healthcare providers, and ensures customer needs are met. Responsibilities include strategic planning, market analysis, and optimizing customer engagement using digital tools.

Oversee drug manufacturing processes ensuring compliance with regulations and quality management. Manage documentation, collaborate with departments, and address quality issues.

The Engineer will support, maintain, and improve automation systems in a pharmaceutical production environment, ensuring compliance and operational stability while collaborating with various teams.

The Head of Value & Pricing leads pricing and access strategies for Novartis in Spain, engaging with health authorities and stakeholders to optimize product value and ensure patient access.

Lead the development of scalable AI solutions for Novartis, integrating advanced machine learning models while collaborating with teams in the US and India.

The Manager Scientific Writing will create and review scientifically accurate promotional content, ensuring compliance with regulations and coordinating with various teams across platforms.

The QA Operations Manager leads quality oversight, batch release, team management, training, and compliance with regulations in pharmaceutical production.

The TRD QA Specialist supports quality assurance in pharmaceutical manufacturing, overseeing compliance, managing quality systems, conducting audits, and maintaining documentation while ensuring adherence to GMP standards.