The Learning & Development/Training Placement Student will assist in designing and delivering training programs, creating training materials, coordinating logistics for sessions, analyzing employee training data, and collaborating on various L&D projects.

The Manager, Safety Surveillance and Risk Management will lead global pharmacovigilance efforts and compliance activities at Viatris. Responsibilities include overseeing Global Periodic Reports, labelling activities, risk management plans, and safety triggers, while providing expertise and training to team members. This role liaises with regulatory departments and ensures adherence to international standards and safety protocols in drug management.

The Head of Global Device Development and Operations at Viatris leads the device and combination product operations, ensuring regulatory compliance and managing the product lifecycle. Responsibilities include strategic oversight of development, commercialization, lifecycle management, and collaboration with multi-functional teams to deliver high-quality medical devices and maintain compliance with local regulations.

The Associate Operator role involves inspecting products, assisting with production equipment setup, maintaining cleanliness in manufacturing areas, ensuring proper labeling and storage of products, documenting production processes, training new staff, and performing equipment calibrations.

The Quality Assurance Documentation Controller will manage the site GMP documentation system, assist in coordinating quality systems, review document changes, manage document distribution, archive quality records, and help with quality-related training and incident management.

The CV Manager at Viatris will design and lead the marketing strategy for the cardiovascular portfolio, ensuring alignment with the sales team and maximizing profitability. Responsibilities include developing sales materials, assessing revenue potential, and implementing an omnichannel strategy while maintaining high compliance standards.

The Senior Quality Assurance Specialist will oversee the Quality Management System, ensuring compliance with regulatory standards and quality objectives. Responsibilities include maintaining documentation, quality oversight of laboratory equipment, data integrity, and supporting audits and inspections.

The Quality Control Analyst I will conduct routine wet chemistry testing of raw materials and products, ensure compliance with GLP and cGMP procedures, participate in validation programs, and support continuous improvement initiatives in the laboratory.

The Customer Experience Coordinator at Viatris is responsible for liaising between external Customer Service providers and internal teams, overseeing performance, ensuring operational alignment, optimizing resource allocation, managing complex customer service issues, and facilitating training programs. This role requires a strategic focus on continuous improvement and effective communication across various departments.

The Senior QA Executive will manage the GMP documentation system, coordinate quality system elements, and support batch documentation issuance. They will also oversee the archiving of quality records and facilitate training for the QA team.

The HR & Engagement Support internship role involves supporting employee engagement initiatives, organizing company events, collaborating with the HR Business Partner on wellness programs, assisting in preparing HR metrics, managing onboarding processes, and facilitating internal communications to boost employee engagement.

The EHS Manager at Viatris ensures compliance with environmental, occupational health, and safety legislations. Responsibilities include developing and executing EHS policies, conducting risk assessments, managing safety programs, and training personnel to promote a safe workplace. They liaise with regulatory agencies and manage EHS personnel, ensuring all operational and compliance targets are met.

The EHS Specialist at VIATRIS will establish and maintain compliance with environmental and safety regulations while implementing EHS management systems. Responsibilities include working on injury management, leading EHS audits, utilizing EHS software, and promoting a safe working environment within the manufacturing industry, particularly in pharmaceuticals or food.

The Office Manager at Viatris will welcome visitors, support HR with onboarding and property tracking, ensure the office runs smoothly, manage supplies, and champion workplace safety initiatives as part of the EHS group.

The Quality Control Analyst II is responsible for performing chromatographic and wet chemistry analyses of materials and products, ensuring compliance with GLP and cGMP procedures, supporting validation programs, and reviewing QC data as assigned.

The Quality Assurance Qualified Person is responsible for ensuring that commercial products are manufactured in compliance with cGMP and regulatory requirements, including batch release. This involves active participation in quality management, oversight of compliance requirements, and the development of performance monitoring indicators. The QP will also provide quality support to operational teams and contribute to continuous improvement initiatives.

The Audit Analytics Data Analyst role at Viatris involves analyzing data sets, developing insights, and making recommendations to enhance internal audit processes. Responsibilities include collaborating on dashboards, sourcing and automating data, conducting quantitative analysis, and presenting findings to stakeholders. The analyst must also ensure data integrity and stay updated on industry trends.

The Sharpen Up Summer Internship Program at Viatris offers students valuable experience through a rotational program across various functions such as Sales, Marketing, HR, and Finance. This three-week internship aims to prepare students for business life by providing hands-on exposure to the pharmaceutical industry.

The R&D Bioanalytical Senior Manager will lead bioanalytical development activities for oligonucleotide and peptide products, focusing on bioanalytical method development, technical support for characterization of DNA/RNA segments, and ensuring compliance with regulatory requirements. Responsibilities include managing the development team, solving problems, and fostering high performance while collaborating with Quality and Regulatory groups.

The Quality Control Analyst Level II at Viatris conducts chromatographic and wet chemistry analyses of various samples, ensures compliance with GLP & cGMP, supports validation programmes, and reviews QC data. They contribute to maintaining product quality and regulatory adherence in a collaborative environment.