Search the 47 jobs at Viatris

The Manager, Global Privacy Operations role involves managing and designing global privacy training, providing operational support for data incidents, and conducting privacy assessments. This position requires oversight of privacy processes and supporting compliance with new legislative requirements.

The R&D Engineer will execute design verification activities, lead the development and validation of test methods, and support the lifecycle of combination products. Responsibilities include technical documentation, statistical analysis of data, ensuring product reliability, and participating in investigations as part of a global device development team.

The Quality Assurance Qualified Person is responsible for ensuring commercial products meet quality and compliance standards in line with cGMP and regulatory requirements. This includes overseeing product flow, performing batch release, supporting operational teams, and providing expertise in quality assurance and compliance issues. The role is crucial for maintaining high product quality and safety in the pharmaceutical industry.

The Digital Marketing Specialist at Viatris will develop and execute the annual digital marketing strategy, collaborating with various teams to optimize customer communication, manage multiple projects, and ensure compliance with legal standards. Responsibilities include monitoring performance metrics and managing external agencies to enhance digital initiatives.

The Portuguese speaking OTC Process Expert will oversee the Order-to-Cash processes including billing, collections, and cash applications. The role involves training team members, resolving issues, ensuring process quality, and contributing to finance transformation through optimization and standardization. It requires strong communication and teamwork skills while coordinating across various functions and managing stakeholder requests.

The R&D Bioanalytical Senior Manager leads bioanalytical development for oligonucleotide and peptide products within R&D, focusing on method development, structural characterization, and regulatory compliance. They manage a team and foster a culture of high performance, while ensuring adherence to quality standards and technical expertise in complex biopharmaceutical analyses.

The Commercial Finance Specialist will be responsible for month closing activities, P&L analysis, price-volume analysis using Excel and Power BI, supporting audits, ERP submissions, handling vendor invoices, and coordinating data for financial reports. The role involves collaboration with internal teams and external vendors, reporting to the Senior FP&A Manager.

The Head of Site EHS will lead the development and implementation of environmental, health, and safety (EHS) programs at the Viatris Troisdorf site. Responsibilities include managing the EHS team, ensuring compliance with local and company standards, conducting audits, leading training initiatives, and developing company-wide EHS strategies to improve safety and compliance.

The Senior Device Design Engineer will work on multi-disciplinary teams to develop technical specifications and designs for drug delivery device technologies. Responsibilities include leading design efforts, creating detailed documentation including specifications and CAD models, problem-solving, and mitigating risks related to combination products.

The Senior EHS Manager will develop, implement, and maintain EHS programs to ensure compliance with regulations and best practices, manage internal audits, lead investigations into incidents, and advise on EHS matters. The role also involves budgeting and EHS risk assessments while promoting a safety-focused culture throughout the organization.

The QA Executive will assist in coordinating elements of the Quality System, perform batch record reviews, manage vendor activities, support investigations and product quality review reports, and prepare KPI data.

This role involves managing cross-functional teams in the development of drug-device technologies. Responsibilities include project planning, resource forecasting, risk management, and communication with stakeholders to ensure successful project execution and alignment with business plans.

The Quality Assurance Executive II will perform batch record reviews, assist with incident report systems, manage quality complaints, and prepare quality reports. This role involves oversight of packaging operations and maintaining quality training programs.

The QA Executive Level III is responsible for managing elements of the Quality Management System, including Change Control, deviation handling, and customer complaints. The role involves leading GMP investigations, conducting audits, and supporting training on quality topics while ensuring compliance with regulations.

The Head of Quality Assurance will lead a team of 8, manage the quality assurance department, ensure adherence to GMP and GDP regulations, and oversee compliance for pharmaceutical operations in Switzerland while collaborating with cross-functional teams for product launches.

The Cleanroom Supervisor oversees filling and jet printing activities to ensure compliance with GMP standards. Responsibilities include leading and coaching production teams, reviewing documentation, ensuring cleanliness in classified areas, tracking consumables, and conducting audits for compliance and improvement. The role involves setting objectives and conducting performance reviews for team members.

The State Account Manager will drive account growth through new business acquisition, exceed sales targets, and manage relationships with pharmacy stakeholders in NSW. Responsibilities include executing business plans, preparing sales proposals, analyzing customer needs, and coordinating with internal teams to optimize service delivery.

The Quality Control Analyst I will conduct wet chemistry analyses of raw materials, in-process products, and stability samples, ensuring compliance with GLP and cGMP. Responsibilities include sampling, supporting validation programs, participating in department projects, and driving continuous improvement initiatives.

The QC Analyst Level II at VIATRIS conducts chromatographic and wet chemistry analysis of samples, ensuring compliance with GMP documentation. Key responsibilities include routine testing, supporting validation programs, method transfers, and reviewing QC data.

The Capability Development Associate at Viatris Limited is responsible for designing and delivering development programs, facilitating events, driving a continuous improvement culture, and providing administrative support. This role aims to enhance capability development across the business, foster collaboration, and maintain a strong workplace culture.