The Senior Manager, Core Labelling Strategy leads regulatory labelling governance for Viatris, ensuring compliance and strategic direction in labelling documentation and processes for pharmaceutical products.

Lead regulatory strategy and compliance for medical devices and drug-device combination products globally. Serve as SME on FDA, EU MDR and ISO standards, guide program teams on regulatory plans and submissions (NDA/ANDA/BLA/MAA), mentor the regulatory team, and support SaMD classification and global IT compliance.

The Labelling Hub Manager oversees regulatory labelling activities, manages associates, coordinates with stakeholders, and ensures compliance with guidelines and legislation.

The Operational Excellence Lead drives transformational change, champions Lean Six Sigma, mentors teams, and implements sustainable process improvements to enhance quality and efficiency.

The Head of Quality Assurance at Viatris oversees quality activities, ensures compliance with regulations, manages QA staff, and drives continuous improvement.

The Director Respiratory Regulatory CMC leads regulatory strategies for respiratory products, managing stakeholder relationships, CMC submissions, and compliance with regulatory agencies to support product development and lifecycle management.

Support OTC operations across cash application, billing, collections, credit and insurance management. Handle reconciliations, invoicing, dispute management, KPI/CTQ reporting, month-end closings, audits, process improvements and stakeholder collaboration, ensuring compliance with SOPs and GAAP.

The Senior Lead Scientist will assess API suppliers, conduct analytical testing, lead method transfers, and interface with teams to ensure compliance and efficiency in drug development processes.

The Senior Manager, Core Labeling Strategy oversees global regulatory labeling, develops core labeling strategies, aligns with regulatory requirements, and ensures compliance across products, while managing a cross-functional team and external collaborations.

The Epidemiology Lead is responsible for developing and executing epidemiology strategies throughout the product lifecycle, ensuring evidence generation for clinical development and market access, collaborating with teams, and applying advanced analytic techniques.

The Manager, Project Engineering is responsible for overseeing capital projects, collaborating with multiple departments, and ensuring compliance with quality and safety practices.

The Senior Manager Sterility Assurance ensures the sterility of injectable products through contamination control, compliance with regulations, and cross-department collaboration.

Support and implement continuous improvement initiatives site-wide by analysing data and processes, presenting prioritized recommendations, coaching stakeholders on OE methodologies (Lean, Six Sigma, TPM), delivering workshops, and driving improvements focused on safety, quality, cost and delivery.

The Regulatory Affairs Officer ensures regulatory compliance, manages product lifecycle, coordinates applications, maintains databases, and collaborates with cross-functional teams to support market availability of medicinal products.

The Statutory Accounting & Controlling Manager leads statutory and compliance accounting for legal entities, oversees monthly and annual reporting, manages audits, and ensures regulatory compliance.

The QC Analyst II performs chromatographic and wet chemistry analysis, supporting validation programs, and ensuring compliance with GMP. This role also involves data review and report writing.

The Sales Representative will provide a great sales experience to GPs and pharmacists, manage territory performance, and achieve sales KPIs through effective communication and strategic planning.

The Regulatory Affairs Lead will direct regulatory strategies, ensure compliance with local regulations, manage a team, and improve regulatory processes through stakeholder engagement.

The Senior Financial Accountant will oversee financial accounting operations, prepare financial reports, manage compliance activities, and partner with shared services teams to enhance processes.

The Director of Regulatory Compliance will establish and lead the Global Regulatory Affairs Compliance function, ensuring adherence to regulatory processes, managing audits, and evolving the Quality Management System while collaborating with cross-functional teams.