Jobs at Viatris

Manage site GMP documentation and QA training systems, control issuance and archival of quality records, review document changes, support batch record reconciliation, coordinate QA training curricula, and report QA performance metrics.

Lead QA operations at a sterile pharmaceutical facility, overseeing Batch Release, incoming inspection, Investigations and CAPA. Ensure cGMP and regulatory compliance, maintain QMS, drive inspection readiness, manage quality metrics, and develop high-performing QA teams including Qualified Persons (QP).

The Finance Operations Manager will oversee site-level financial activities, including cost accounting, budgeting, forecasting, and compliance, while partnering with leadership to drive performance optimization and profitability.

The Senior Manager will oversee European regulatory policies, lead intelligence reports, and ensure strategic engagement with health authorities, providing actionable insights for regulatory compliance.

The French-speaking OTC Senior Analyst supports the OTC team in Cash Application, Billing, Collection, and Credit Management, ensuring compliance with SOPs and achieving KPIs while resolving issues and improving processes.

Lead global commercial strategy and launch planning for Selatogrel, owning long-range commercial plans, go-to-market models, budget, performance metrics, and cross-functional alignment with Market Access, HEOR, Finance, and affiliates to ensure launch readiness and lifecycle growth.

The Director Regulatory CMC Sciences manages complex global regulatory projects involving site transfers and API sourcing, ensuring effective collaboration and compliance across teams while mitigating regulatory risks.

Measure and optimize ROI of medical visits, samples, and promotional investments across LATAM. Build activity-to-impact models, monitor field force productivity, standardize impact metrics and dashboards, provide impact assessments to leadership, support resource allocation and incentive alignment, and collaborate with Sales, Marketing, and Global teams to embed compliant, data-driven decision making.

The role involves leading regulatory project management for complex manufacturing changes, ensuring compliance, and collaborating with internal stakeholders to optimize processes.

Perform quantitative chemical and microbiological analyses of APIs and related materials using instruments (HPLC, GC, FTIR, UV/VIS). Prepare reagents, perform calculations, maintain lab records, organize samples, support data review, follow SOPs and safety procedures, and assist Group Leader with daily lab activities.

Two-year graduate development programme with three rotations across pharmaceutical site departments (Production, Automation, Engineering, EHS, Quality, Supply Chain, Regulatory Affairs, OpEx). Participants work on impactful projects, receive mentorship and training, gain technical and business skills, and attend career and STEM outreach events. Locations across multiple Irish sites with career progression opportunities within Viatris.

Two-year graduate programme launching September 2025 with three structured rotations across pharmaceutical site departments (e.g., Production, Automation, Engineering, EHS, Quality, Supply Chain, Regulatory Affairs, OpEx). Participants work on impactful projects, receive mentorship and training, attend career and STEM events, and gain practical pharmaceutical operations experience with clear career progression opportunities.

Two-year graduate development programme with three structured rotations across pharmaceutical site departments (e.g., Production, Engineering, Quality, Supply Chain). Participants work on impactful projects, gain hands-on operational experience, receive mentorship and training, attend career and outreach events, and follow a clear pathway for career progression within the company.

Drive sales force effectiveness across incentive compensation, CRM/SFA operations, field analytics, and commercial performance reporting. Manage incentive calculations and platforms, ensure CRM and master data quality, design targeting/segmentation and KPIs, produce executive reports and dashboards using Power BI/SQL, and apply AI tools to improve field productivity and decision-making.

Lead warehouse and 3PL distribution operations across NZ, ensure GMP compliance, inventory accuracy, and safety. Drive continuous improvement in logistics, freight, forecasting and demand planning. Manage team capability, training, certifications, and stakeholder relationships to meet service, cost, and audit objectives.

As the Global Regulatory Business Process Lead, you will optimize regulatory processes, ensure adherence to compliance, and utilize data analytics for continuous improvement. You'll collaborate cross-functionally and lead training initiatives.

Lead and develop multidisciplinary maintenance and engineering teams to design and execute multi-year maintenance and capital strategies. Drive equipment reliability, asset lifecycle management, preventive maintenance, RCM (FMECA/FMEA), validation (IQ/OQ/PQ), and regulatory compliance (HPRA, FDA, cGMP, Annex I). Manage capital budgets, partner with Manufacturing/Quality/Supply Chain, and support audits and sustainability initiatives.

Provide high-quality customer service to Viatris customers via phone and email; build customer relationships; process orders, credits and returns; and liaise with cross-functional teams to handle ad hoc requests. Report to the National Virtual Pharmacy Manager and support business needs for the virtual pharmacy.

The Senior Labeling Specialist prepares and submits product labeling for regulatory compliance, interacts with multiple departments, and manages projects efficiently while adhering to FDA regulations.

Lead global brand strategy and launch readiness for Cenerimod, translating Phase 3 data into compliant brand narratives, coordinating cross-functional launch teams, managing global marketing budget and vendors, supporting market access and HEOR alignment, and ensuring regulatory and compliance governance across regions.