Teams at Alvotech

Provides technical and engineering support for upstream and downstream drug substance manufacturing. Responsibilities include process optimization, troubleshooting, deviation investigations, root cause analysis, CAPAs, change controls, validation, technology transfers, documentation, data analysis, equipment qualification, audits, and cross-functional collaboration across GMP biologics operations.

Leads cross-functional operational excellence and continuous improvement initiatives, optimizing processes, reducing waste, and improving efficiency, quality, compliance, and scalability. Manages strategic transformation projects, facilitates process mapping and redesign, builds improvement capabilities, coaches stakeholders, and supports GMP compliance, inspection readiness, risk assessments, investigations, and CAPA activities. Uses data-driven problem solving and change leadership to deliver measurable, sustainable business improvements.

Leads product quality complaint investigations from initiation through closure, conducting root cause analysis, assessing product impact, managing CAPAs, and ensuring GMP compliance. Collaborates cross-functionally with manufacturing, suppliers, quality control, engineering, and supply chain teams. Identifies continuous improvement opportunities within the quality management system and manages multiple investigations according to established timelines and regulatory expectations.