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**Summary**:Are you ready to take your career to the next level?
Look no further!
Novartis Ag is seeking an individual who demonstrates exceptional talent and enthusiasm to join our team as a Digital Quality Control Analyst.
This is a unique opportunity to work with a world-class organization that is dedicated to improving the lives of millions of people around the globe.
**About the Role**:**Responsibilities**- Lead the implementation and management of Labware (GLIMS), a global laboratory information management system, within three QC labs in the region, ensuring seamless integration and effective utilization of the system.- Collaborate with cross-functional teams, including IT, QC, QA and lab personnel, to gather requirements, design workflows, and configure Labware (GLIMS) to meet the specific needs of each lab.- Customize Labware (GLIMS) functionalities and workflows to streamline quality control processes, automate data management, and ensure regulatory compliance.- Conduct thorough testing and validation of Labware (GLIMS) functionalities to ensure accuracy, compliance, and data integrity.- Develop and maintain standard operating procedures (SOPs) for Labware (GLIMS) usage, ensuring that all lab personnel are trained on the system and adhere to established protocols.- Provide ongoing technical support and troubleshooting for Labware (GLIMS) users, addressing any issues or concerns promptly and effectively.- Monitor and analyze data generated by Labware (GLIMS), identifying trends and potential areas for improvement in quality control processes.- Collaborate with the Quality Assurance team to ensure Labware (GLIMS) implementation aligns with regulatory requirements, including Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).- Stay updated with the latest advancements in digital quality control systems, specifically Labware (GLIMS), and recommend enhancements or additional tools to improve efficiency and effectiveness.
**Qualifications**- Bachelor's degree in a relevant scientific discipline, such as Chemistry, Biology, or Pharmaceutical Sciences.- Strong knowledge of quality control processes and regulations, including Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).- Proficiency in configuring and customizing Labware (GLIMS) workflows and functionalities to meet specific lab requirements.- Excellent problem-solving skills, with the ability to troubleshoot and resolve technical issues related to Labware (GLIMS) implementation.- Detail-oriented approach, ensuring accuracy and data integrity within the system.- Strong communication and interpersonal skills, enabling effective collaboration with cross-functional teams and training lab personnel.- Ability to work independently and manage multiple projects simultaneously, ensuring timely completion of tasks.- Familiarity with regulatory requirements for digital systems in the pharmaceutical industry