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Support day to day supplier management activities, assist in supplier onboarding, monitoring, documentation deliverables, and report creation, while attending necessary meetings.
The R&D Bioanalytical Senior Manager will lead bioanalytical development for oligonucleotide and peptide complex injectable products. Responsibilities include developing methods for structural characterization and quality control testing, influencing regulatory requirements, and solving bioanalytical challenges.
The Commercial Finance Specialist at Viatris will engage in month closing activities, P&L analysis, price-volume analysis using Excel and Powerbi, and support audits. Responsibilities also include ERP submissions, invoice management, asset disposal reporting, and coordination of financial data. The role requires strong analytical skills and advanced proficiency in finance-focused software.
The QA Team Leader is responsible for overseeing the Quality Assurance Department, ensuring compliance with GMP, managing staff performance, and implementing quality metrics. They will foster collaboration within the team and with other departments, providing guidance and training while maintaining high standards of product quality.
The Senior Scientist/Engineer will oversee testing for injectable combination products, provide technical expertise and mentorship, lead development and validation of test methods, ensure compliance with design verification guidelines, and manage documentation within Global Device Development, contributing to the reliability and success of combination products.
The Quality Assurance Specialist will manage and improve the Quality Management System by overseeing laboratory activities, validating test methods, managing CAPA processes, and ensuring compliance with regulatory requirements. The role involves data analysis for performance measurement and support during third-party inspections and audits.
The Qualified Person role at Viatris involves ensuring compliance with legislation requirements for manufacturing pharmaceutical products, certifying product batches for sale, approving suppliers, investigating non-conformances, and participating in audits and inspections. Candidates should have a M.Sc. in Life Sciences and at least 1 year of experience in a pharmaceutical company.
The Commercial Compliance Specialist will support North America commercial business initiatives, focusing on compliance through field ride-alongs, policy development, compliance training, and conducting risk assessments. Approximately 80% of the role involves executing field ride-alongs to identify compliance risks and trends, while the other 20% focuses on compliance guidance and policy enhancement.
The Principal IT ERP - Record to Report role involves leading the analysis, design, and deployment of SAP FI/CO solutions. Responsibilities include guiding local teams on configuration for RTR processes, leading global teams to deliver SAP projects, and ensuring best practices in SAP configuration. The role also requires engaging with stakeholders to enhance business value and solving complex system issues for SAP RTR integration.
The Veeva CRM Manager leads the technical management of Salesforce and Veeva CRM systems, overseeing solution development, improving functionality, and collaborating with teams to resolve issues and innovate processes. They act as a liaison between IT and business, providing expertise and documentation for CRM functionalities and enhancements.
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