Join a leading company as a Maintenance Systems Administrator and be part of exciting projects in vaccine development and production.
Key Responsibilities:
* Register new equipment and instrumentation on the Computerised Maintenance Management System (CMMS) following change control procedures.
* Update the supplier quality management systems for spare parts following change control procedures.
* Manage documentation in relation to the CMMS and supplier quality management system.
* Work with stakeholders on the approval and execution of the above.
Requirements:
* Good data management skills.
* Experience / proficiency in document management systems and office applications.
* Experience working in a Good Manufacturing Practice (GMP) environment and quality management systems.
* Familiar with Maintenance Systems structure and applications.
* Analytical mindset, data driven with attention to detail on systems.
This is a fantastic opportunity to work with a Centre of Excellence in the industry. You will have the chance to work on critical investment projects both on-site and remotely.