Optimize project execution by leading cross-functional teams in the support and validation of manufacturing systems, addressing technical challenges and compliance requirements to enhance operational efficiency.

Contribute to GxP compliance by supporting Pharmacovigilance, Clinical, and Regulatory Affairs systems, ensuring robust validation and adherence to regulations while collaborating with Quality and IT teams to streamline operations.

Lead compliance efforts for GxP systems in Pharmacovigilance, Clinical, and Regulatory Affairs. Engage with Quality and IT teams to ensure systems meet regulatory standards, develop validation deliverables, and conduct compliance reviews.

Drive your career forward by ensuring data integrity through meticulous audit trail reviews in a collaborative setting, supporting both manufacturing and QC laboratory systems to uphold compliance and quality standards.

Contribute to critical validation processes in a dynamic team environment, ensuring compliance and operational excellence. Engage in hands-on activities involving IQ/OQ protocols and assist with innovative engineering solutions.