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The QC Analyst - Micro role involves analyzing raw materials and products, monitoring manufacturing areas, and performing method validations while adhering to GMP standards.

The Senior Specialist will oversee global regulatory operations, ensuring compliance with EU regulations, managing data governance, and leading process improvements within regulatory initiatives.

As the Global Regulatory Business Process Lead, you will optimize regulatory processes, ensure adherence to compliance, and utilize data analytics for continuous improvement. You'll collaborate cross-functionally and lead training initiatives.

Lead regulatory strategy and compliance for medical devices and drug-device combination products globally. Serve as SME on FDA, EU MDR and ISO standards, guide program teams on regulatory plans and submissions (NDA/ANDA/BLA/MAA), mentor the regulatory team, and support SaMD classification and global IT compliance.

The Director of Regulatory Compliance will establish and lead the Global Regulatory Affairs Compliance function, ensuring adherence to regulatory processes, managing audits, and evolving the Quality Management System while collaborating with cross-functional teams.

The Senior QC Analyst will analyze raw materials and products, review analytical data, conduct method validations, and provide training while ensuring compliance with regulations.

Drive order fulfillment and transactional activity across the supply network using SAP/ERP: create and manage POs, SOs, inbound/outbound deliveries, invoices, reporting, KPI analysis, process documentation, stakeholder liaison, and reporting for supply chain operations.

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.

The Operational Excellence Lead drives transformational change, champions Lean Six Sigma, mentors teams, and implements sustainable process improvements to enhance quality and efficiency.

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.