E - System Engineer - The E-System Engineer supports the implementation maintenance and lifecycle management of electronic systems (e.g. MES LIMS QMS DMS ERP and historians) in a GxP-regulated life science manufacturing environment. The role ensures systems are validated secure and compliant with 21 CFR Part 11 EU Annex 11 and data integrity (ALCOA+) requirements while providing reliable technical support and driving continuous improvement.
Responsibilities
- Configure administer and maintain GxP electronic systems such as MES LIMS QMS document management and ERP-related applications
- Provide L2/L3 technical support troubleshoot incidents and perform root cause analysis to minimize downtime
- Prepare and execute CSV deliverables per GAMP 5 including validation plans URS risk assessments IQ/OQ/PQ and traceability matrices
- Ensure compliance with 21 CFR Part 11 EU Annex 11 and data integrity requirements including audit trails and electronic signatures
- Manage user access roles security and master data in line with defined SOPs and periodic review requirements
- Author and manage change controls deviations CAPAs and impact assessments to keep systems in a validated state
- Support system integrations and interfaces between shop-floor laboratory and enterprise systems
- Plan and support system upgrades patches migrations backups and disaster recovery testing
- Collaborate with Manufacturing QA IT and Automation teams to gather requirements and support new projects and tech transfers
- Maintain SOPs and system documentation train end users and support audits and regulatory inspections