Quality Lead in Pharma Development

Shape the future of healthcare quality management as a Quality Lead s role emphasizes developing quality strategies, conducting audits, and supporting regulatory compliance.

In this key position within Pharma Development Quality, you will enhance our quality assurance practices across global processes. Your expertise in GVP and GCP will be instrumental in ensuring compliance while influencing innovative therapy development. Collaborate with international stakeholders to drive audit insights and prepare for regulatory inspections.

Key Responsibilities:

• Drive risk-based Quality Assurance strategies utilizing the CtQ framework

• Lead and perform global audits to compile valuable quality data

• Foster partnerships with stakeholders to communicate audit findings

• Support regulatory authority inspection efforts and planning

• Participate in initiatives for continuous improvement of PDQ processes

Requirements:

• Bachelor’s degree or equivalent in a scientific or quality field

• Industry experience in pharmaceuticals, biotech, or medical devices

• Deep understanding of global GxP regulations

• Strong digital and analytical reporting capabilities

• Proven problem-solving and project management skills

Elevate Roche’s quality management with your expertise and proactive approach in developing compliance strategies.
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