Job Title

Strengthen QC processes as a QC eSystems Specialist. Expertly manage quality management systems and electronic laboratory systems, ensuring compliance with global GMP and CMC standards. This role is crucial for supporting the QC Quality Management System and its continuous improvement. You''ll oversee the administration of electronic QC systems, contribute to data architecture design, and ensure compliance with regulatory requirements. Your collaboration with various teams will enhance the QC operational framework. Key Responsibilities: Oversee and maintain QC eSystems and master data Support implementation of QC Quality Management System Contribute to the design of QC data architecture Conduct user training and develop relevant documentation Facilitate investigations and CAPAs for QC eSystems Requirements: 3+ years quality systems management experience Bachelor''s degree in a scientific or engineering discipline 5+ years of experience in biotechnology or pharmaceuticals Strong understanding of eSystems in GxP environments Proactive identification of improvement opportunities Utilize your expertise to enhance quality systems and ensure compliance, driving effectiveness in QC laboratory operations. #J-18808-Ljbffr