Jobs at Viatris

Manages local brand and portfolio strategy for generic medicines and selected consumer healthcare brands in Portugal. Responsibilities include lifecycle management, market and competitive analysis, brand planning, customer engagement, cross-functional leadership, promotional execution, budgeting, forecasting, KPI monitoring, and profitability improvement. The role adapts global priorities to the Portuguese pharmaceutical market and supports sales teams through strategic guidance, training, and compliant commercial materials.

Performs inventory valuation, obsolescence analysis, SAP product costing, cost maintenance, financial controls, reconciliations, audits, month-end and quarter-end close activities. Supports forecasting, budgeting, business analysis, and process improvements while maintaining accurate and compliant financial information for operations.

Manage a pharmaceutical sales territory by achieving revenue and market-share targets, developing healthcare-provider relationships, identifying business opportunities, executing brand and CME plans, maintaining CRM activity, managing budgets, and complying with pharmaceutical regulations. The role requires territory planning, customer engagement, market intelligence, administrative reporting, adverse-event reporting, and collaboration with internal stakeholders. Occasional evening, weekend, and business travel may be required.

Analyzes raw materials, in-process materials, and finished pharmaceutical products. Reviews analytical data and reports, performs peer reviews, method transfers, compendial verifications, and instrument qualification and troubleshooting. Generates protocols, supports complex projects, trains team members, and follows GMP, SOP, environmental, health, and safety requirements.

Manages U.S. advertising and promotion regulatory affairs for pharmaceutical products, including regulatory strategies, promotional material reviews, labeling activities, submissions, FDA liaison work, and PRC participation. Partners with Commercial, Clinical, Legal, Marketing, and Sales teams to mitigate regulatory risk, support brand plans, provide risk-benefit guidance, deliver training, and ensure compliance with FDA requirements.

Creates and maintains pharmacovigilance case files, reconciles individual case safety reports, prepares correspondence, maintains the PSRM file room, supports reimbursement processing, and performs administrative tasks including filing, mail handling, inventory tracking, and database entry. The role requires adherence to detailed procedures, confidentiality, strong communication and organizational skills, and proficiency with Microsoft Office and Outlook.

Performs routine wet chemistry testing of raw materials, in-process, finished, and stability samples under GLP and cGMP procedures. Samples materials and water, supports process and method validation programs, completes GMP documentation, and participates in laboratory continuous improvement and departmental projects. Requires strong analytical, communication, teamwork, organization, chemistry, and computer skills.

Conduct analytical testing for respiratory product development, clinical studies, stability, scale-up, and commercialization. Plan and lead experiments, interpret data, troubleshoot instrumentation and unexpected results, maintain cGMP documentation, and support laboratory operations. Coordinate with multidisciplinary teams, oversee junior laboratory staff, ensure EHS, GMP, GCP, quality, and compliance adherence, and identify improvements to laboratory practices.

Manages global CMC regulatory affairs activities across the pharmaceutical development and manufacturing lifecycle. Prepares regulatory strategies, submissions, post-approval variations, renewals, and responses to agency queries. Assesses regulatory risks, tracks commitments and timelines, ensures global compliance, and collaborates with R&D, Quality, and Regulatory teams. Provides technical guidance and mentors colleagues on complex CMC regulatory matters.

Plans, delivers, and optimizes digital marketing campaigns, customer engagement journeys, and omnichannel activities for UK healthcare brands. Manages email, websites, CRM, SFMC, social media, webinars, analytics, and other digital platforms. Uses customer and campaign insights to improve engagement and outcomes, manages agencies and stakeholders, monitors trends, and ensures compliance with pharmaceutical, pharmacovigilance, data privacy, and industry requirements.

The Manager, Regulatory Affairs Brands CMC prepares global CMC regulatory submissions and strategies across the pharmaceutical product lifecycle. Responsibilities include regulatory assessments, post-approval changes, renewals, agency responses, risk management, regulatory commitment tracking, and collaboration with R&D, Quality, and Regulatory teams. The role also provides technical guidance, mentors colleagues, and ensures global regulatory compliance with external requirements and internal procedures.

Leads technical services for externally manufactured respiratory pharmaceutical products. Responsibilities include managing contract manufacturing organizations, technology transfers, GMP investigations, CAPA closure, process improvements, capacity planning, vendor negotiations, experimental design, and cross-functional project execution. The role oversees technical projects, budgets, timelines, product performance data, and manufacturing reliability while partnering with R&D, Quality, Supply Chain, Sourcing, and Manufacturing teams.

The Sell-Out Performance Sr Manager will drive Viatris' sell-out strategy, managing budgets, executing trade initiatives, and promoting a performance-driven culture to enhance market presence and profitability.

Manages pharmaceutical quality systems supporting batch disposition, complaints, deviations, CAPAs, change controls, supplier qualification, quality agreements, product returns, PQRs, SOPs, training systems, risk assessments, self-inspections, and compliance with GMP, GDP, and GxP requirements. The role also coordinates investigations, vendor oversight, quality documentation, KPIs, and implementation of the regional Quality Management System.

Creates sales performance reports and dashboards, manages relational data, supports sales force alignment and targeting, and provides analytical support to Sales, Marketing, Finance, and other stakeholders. The role validates and supports sales reporting tools, documents processes, collaborates across departments, and handles ad hoc analytics and special projects.

Develop localized pharmaceutical brand strategies, analyze market intelligence, manage forecasting and budgets, coordinate cross-functional commercial, medical, and regulatory teams, engage key opinion leaders, support field execution, and monitor campaign KPIs. The role requires therapeutic expertise, strong analytical and organizational skills, English fluency, a clean driving license, and travel availability. This is a fixed-term two-year contract.

Manages pharmaceutical supply chain quality, sanitary responsibility, product disposition, GMP/GDP compliance, recalls, deviations, complaints, change controls, audits, contractor quality oversight, and regulatory authority liaison activities. Maintains the affiliate Quality Management System, training programs, inspections, quality metrics, corrective actions, and product release processes while ensuring compliance with Mexican pharmaceutical regulations.

Provides administrative and scheduling support to GRA leaders and teams, including meeting coordination, travel booking, expense reports, calendar management, presentations, meeting summaries, onboarding support, organizational chart maintenance, recruitment assistance, confidential information handling, and IT request management.

Leads global drug delivery device development programs from concept through registration and launch. Manages integrated plans, resources, budgets, risks, schedules, scenario analyses, contracts, and internal and external partners. Provides technical project leadership, monitors critical milestones, resolves conflicts, and supports development decisions while promoting quality management and environmental, health, and safety compliance.

Conducts quantitative bioanalysis supporting bioequivalence and pharmacokinetic studies. Operates and troubleshoots HPLC and mass spectrometry equipment, develops and validates analytical methods, documents laboratory work under GLP, reviews data and reports, resolves analytical issues, and provides technical guidance to junior staff.