Validation Expertise Required
Catalyx partners with life science and other highly regulated organisations to enhance efficiency and drive success.
* Manage IT systems qualification, including hardware, software, and infrastructure within a GMP lab setting.
* Validate software applications used in manufacturing, quality control, and other pharmaceutical processes.
* Collaborate with software vendors to ensure system validation documentation is complete and accurate.
Key responsibilities include managing the lifecycle of validated software, performing periodic reviews of validated systems, developing and maintaining traceability matrices, and preparing validation summaries, deviation reports, and corrective/preventive action plans.
Required Skills and Qualifications:
* Strong understanding of regulatory standards and industry best practices.
* Excellent collaboration and communication skills.
* Able to work independently and manage multiple projects simultaneously.
Benefits:
This role offers an opportunity to work in a dynamic and challenging environment, with opportunities for professional growth and development.