Jobs at Viatris

Leads continuous improvement initiatives and technical solutions for high-speed, automated pharmaceutical manufacturing equipment. Supports manufacturing processes, resolves complex equipment and process issues, analyzes performance data, prepares technical reports, and collaborates cross-functionally to improve quality, compliance, reliability, and productivity. The role requires autonomous prioritization, project leadership, strong problem-solving skills, and expertise in regulated drug or medical-device manufacturing environments.

Leads respiratory bioequivalence strategy for product development programs, including study design, analytical testing, regulatory submissions, technical reports, and agency interactions. Partners with clinical, preclinical, statistical, formulation, and device experts to optimize in-vitro and in-vivo performance. Provides scientific recommendations, monitors regulatory guidance, represents the company externally, mentors colleagues, and helps develop bioequivalence function capabilities.

Leads cardiovascular portfolio strategy, product lifecycle management, long-term business planning, brand marketing, product launches, sales forecasting, budgeting, compliance, and promotional approvals. Manages market and competitor analysis, identifies growth opportunities, guides strategic execution, and leads the CV marketing team through coaching, performance management, talent development, and cross-functional collaboration.

Leads financial planning, reporting, forecasting, budgeting, US GAAP close activities, P&L and profitability analysis, working capital and CAPEX management, audit coordination, and finance transformation initiatives. Acts as a strategic finance business partner to commercial and marketing functions, delivering performance insights, business cases, variance analysis, and decision support. Oversees global financial submissions and develops Power BI-enabled reporting and analytics.

Supports global treasury operations by preparing daily cash reports, managing liquidity visibility, building cash flow forecasts, analyzing forecast-to-actual variances, and providing treasury guidance to stakeholders. The role partners with Treasury, Accounting, project teams, and subsidiaries, supports audits, contributes to process improvements and treasury technology initiatives, and helps resolve treasury-related matters.

Partner with local and regional leadership to lead annual budgeting, monthly forecasting, profitability and pricing analysis, and S&OP financial alignment. Own monthly/quarterly reporting, maintain product master data, support NPIs, and build dashboards and automated tools to streamline financial processes and deliver actionable insights.

Promote pharmaceutical products to healthcare professionals and pharmacies across an assigned territory. The representative will achieve sales targets, implement trade policies, analyze territory and sales data, maintain customer profiles, monitor purchasing patterns, and attend sales meetings, medical conferences, and national programs. The role focuses on CVRM products and requires pharmaceutical or medical sales experience, strong negotiation and presentation skills, English proficiency, and a driving license.

Leads Lean 4.0 and operational excellence deployment across pharmaceutical manufacturing sites in Europe and North America. Responsibilities include transformation roadmaps, Lean and digital integration, cost reduction, KPI and performance systems, smart quality, predictive maintenance, energy optimization, and capability building. The role requires multi-site transformation leadership, Six Sigma expertise, Industry 4.0 experience, and knowledge of cGMP and regulatory requirements.

Soporte al equipo de Customer Relations/Master Data en la relegalización de clientes: buscar, recopilar y adjuntar documentación en SAP (XD01/XD02/XD03), organizar cargas, validar registros bajo supervisión, gestionar incidencias y coordinar con Master Data, Customer Support y Calidad para resolver discrepancias y cumplir plazos del proyecto 2026.

Manages key traditional-trade accounts, including wholesalers, distributors, pharmacy chains, and independent retailers. Develops account plans, negotiates commercial terms, drives sales and profitability, coordinates product availability, manages trade investments, and leads joint business planning. Analyzes sales performance, forecasts demand, evaluates promotions, identifies growth opportunities, and collaborates with Marketing, Supply Chain, Finance, and commercial teams to improve sell-in, sell-out, distribution, and market share.

Develops, delivers, and maintains technical, compliance, and non-technical training programs within a pharmaceutical environment. Designs courseware and evaluation tools, maintains curricula and training metrics, ensures employee qualification and knowledge transfer, and keeps documentation inspection-ready. The role collaborates with department leaders and subject matter experts while applying cGMP, GDP, SOP, adult-learning, and instructional-design principles.

Supports pharmaceutical business development across emerging markets by identifying and evaluating portfolio opportunities, conducting market and competitive analysis, building financial models and business cases, coordinating cross-functional diligence, assessing commercialization viability, and advancing deals toward sourcing and closure.

Lead risk management activities for medical devices and combination products throughout development. Maintain ISO 14971 and design control documentation, assess and mitigate product risks, support regulatory submissions and change controls, and partner with Device Development, Clinical, Pharmacovigilance, Quality, and Regulatory Affairs teams. Serve as the risk management subject matter expert while driving quality system and continuous improvement initiatives.

Manages institutional pharmaceutical accounts across North and South Carolina, selling generic injectables and branded products. Responsibilities include analyzing sales, pricing, contracts, GPO awards, customer purchasing, inventory, shortages, and competitor activity. Builds hospital and healthcare customer relationships, supports RFPs and contract compliance, collaborates with supply chain and sales teams, maintains account records, and participates in conferences and advisory boards. Requires pharmaceutical or medical sales knowledge and travel throughout the territory.

Develops and maintains global core and market-specific pharmaceutical labeling, including CCDS, USPI, and EU SmPC. Supports labeling strategy, regulatory submissions, target product labeling, competitive analysis, and responses to health authorities. Partners with Regulatory, Medical, Safety, and Clinical teams, chairs labeling teams, evaluates scientific and regulatory data, and reviews promotional materials for compliance. Requires significant global labeling experience and typically 3–5 years in a relevant scientific, medical, or pharmacy field.

Leads statutory accounting and controlling for multiple legal entities, overseeing US GAAP close processes, local statutory reporting, financial statements, reconciliations, tax accruals, filings, and internal and external audits. Manages assistant managers, supports compliance with SOX and statutory regulations, coordinates stakeholders, and contributes to ERP implementation, process standardization, and automation initiatives.

The Head of Business Development for Europe will lead business development activities focused on generics, partnerships and innovative brands, aligning strategies with commercial leadership and mentoring a BD team.

Manage a designated territory to service pharmacy accounts, exceed dispensary and OTC sales targets, build account loyalty, execute quarterly business plans, use analytics and deal strategies, resolve customer issues, and consistently record call outcomes in the required system.

Develops territory business plans, achieves sales goals, manages customer relationships, and communicates pharmaceutical product information. The representative uses Salesforce, Microsoft Office, Zoom, and CRM tools to manage daily activities, prepares pre-call strategies, negotiates with customers, meets performance targets, and collaborates cross-functionally. The role requires continuous learning, strong communication skills, product knowledge, and approximately 10% travel.

Coordinates pharmaceutical packaging artwork for regional launches and lifecycle projects. Creates and manages regulatory artwork templates, mock-ups, and submission materials; reviews designs for EMA and national Health Authority compliance; validates packaging data; manages change controls in TrackWise; monitors project KPIs; and oversees pictogram governance and color standards for non-branded products.