Description:
An MES Analyst – IT Manufacturing is required to join a join a greenfield biotech manufacturing site in Limerick. This position supports and develops Manufacturing Execution System (MES) electronic batch records and logbook, associated tools, and system interfaces to fulfil business needs. Deploys existing systems, analyses information, designs, programs and/or implements new systems or enhancements to existing systems in accordance with company standards and guidelines.
The Role
- Creates, modifies and/or enhances business applications and/or systems to satisfy business information demands.
- Identify recommend and Implement application software solutions
- Ensure compliance with Computer Systems Validation policies, standards, procedures and/or practices.
- Creates and/or follows MQ IDS applicable procedures and standards. Ensures support projects and/or requests are in accordance with the site strategy for applications architecture.
- Keeps systems and/or applications on current and/or supported versions.
- Keeps close communications with customers during the development cycle or support phases of systems supported.
- Trains and/or assists systems users in the proper use of business applications.
The Person
- Bachelor’s Degree in Information Technology, Computer Science, Engineering or related field (Level 8 or equivalent).
- Minimum 5 years experience in manufacturing, preferred in pharmaceutical or other regulated industries.
- Manufacturing Execution System platform experience required (Syncade, PharmaSuite, Pas-X) Computer Systems Validation in cGMP regulated operations experience
- Knowledge of System Development Life Cycle.
- cGMP's.
- Knowledge of Microsoft Office suite of tools.