Jobs at Viatris

Lead global regulatory labelling strategy and delivery for assigned products, developing and maintaining core and territorial labelling (CCDS, TPL, USPI, EU SmPC). Provide scientific and regulatory assessment, cross-functional alignment with Medical, Safety, and Clinical teams, review promotional and regulatory materials, chair product labelling teams, and support major submissions and health authority interactions while ensuring compliance with SOPs and evolving regulations.

Lead regulatory strategy and execution for medical devices and drug-device combination products. Author and review regulatory submission content (NDA, ANDA, BLA, MAA, NBOp), guide Device Program Teams on compliance with FDA, EU MDR, ISO standards, and design controls, and support team development and cross-functional collaboration to align regulatory plans with program timelines.

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.

The Key Account Manager WHL is responsible for driving sales growth, managing relationships with traditional trade customers, and developing strategic account plans.

The Senior Manager, Global Device Quality leads quality system improvements ensuring compliance with global medical device regulations, collaborates on corporate quality initiatives, and interacts with regulatory authorities while managing compliance and audit activities.

Lead development and validation of test methods for combination products, provide lab technical expertise and mentorship, oversee testing at external facilities, perform statistical analysis and trending, compile technical and regulatory documentation, support investigations and R&D lab activities, and ensure compliance with regulatory and EHS requirements.

The Director of Market Access will lead pricing, reimbursement, and access strategies in Spain, collaborating across functions and engaging stakeholders to ensure the medicines' value is communicated and supported.

Lead end-to-end technical program management for global drug-delivery device development from concept through registration and launch. Own project plans, resource forecasts, risk registers, budgets and contracts; drive cross-functional partner alignment, scenario analyses, risk management, and timely reporting while promoting QMS and EHS compliance.

Support planning, creation, and distribution of promotional materials for assigned CVMET brands; assist with events, budget monitoring, administrative tasks, invoice and purchase order coordination, and regulatory communications. Provide logistical support for meetings and contribute to marketing activities under mentorship during a paid six-month internship (extendable).

No specific responsibilities are listed in the job description. The posting only describes the company and benefits; the role title suggests an entry-level marketing trainee position supporting marketing activities and learning core marketing functions.

The Portuguese-speaking Senior OTC Analyst supports the OTC team in Cash Application, Billing, Collection, and Credit Management, ensuring compliance and efficiency in processes while addressing customer issues and managing accounts.

Coordinate creation, review, approval and implementation of pharmaceutical packaging artwork. Manage artwork requests, briefs, design checks, SKU records, and communicate implementation to packaging sites while ensuring regulatory compliance and escalating issues.

The Director of Regulatory Affairs CMC is responsible for strategic CMC regulatory approaches and managing relationships with stakeholders to ensure compliance and efficiency in regulatory submissions.

The Senior Manager, Regulatory Affairs manages global regulatory compliance, prepares submissions, leads CMC activities, collaborates with teams, and mentors colleagues.

Oversee Design Assurance for medical devices, manage technical documentation, and support manufacturing transfer while ensuring compliance with regulations.

The Head of US Regulatory Affairs Advertising and Promotion leads compliance of promotional materials with regulations and implements strategic regulatory leadership while managing a team and collaborating across departments.

The Planning Master Data Analyst manages planning master data across SAP and advanced systems, ensuring data quality and collaboration across global supply chain teams, particularly during the SAP S/4HANA transformation process.

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 end-to-end marketing strategy for the CNS portfolio to drive sales, ROI, and revenue. Develop data-driven campaigns, omnichannel tactics, cross-functional alignment, performance monitoring, and tools for the sales force. Ensure regulatory compliance, stakeholder mapping, and team development to execute growth-focused product lifecycle plans.

Manage global legal budget planning, forecasting, and vendor payments; build financial models and variance analysis; partner with counsel and finance to optimize legal spend and report performance; drive process improvements and participate in strategic initiatives.