Anna Hrehlevych
ConsultantJob Description
Key Responsibilities
- Maintain and continuously improve MES systems, standards and architectures
- Provide technical support, troubleshooting and system optimization
- Support MES enhancements, upgrades, deployments and lifecycle activities
- Maintain electronic batch records (EBR) and manufacturing workflows
- Prepare and review GxP documentation, specifications, risk assessments, testing documentation, change controls and SOPs
- Support commissioning, qualification and validation
- Integrate MES with automation systems, historians, ERP and other manufacturing applications
- Work closely with Automation, IT, Validation, Quality and Manufacturing teams
- Ensure data integrity, cybersecurity and GMP compliance
- Degree in Automation Engineering, IT, Computer Science, Electrical Engineering or a related discipline
- Hands-on experience with MES / Manufacturing IT / OT systems in a pharmaceutical, biotech or life sciences environment
- Experience with MES platforms such as PAS-X, Syncade, PharmaSuite, Opcenter or similar
- Good understanding of GMP, GAMP, GxP and CSV
- Understanding of manufacturing processes, batch execution and electronic records
- Knowledge of IT/OT infrastructure, industrial networking, VMware and server environments
- Experience integrating MES with ERP, historians and automation platforms
- English and/or German
By applying for this role, you consent to SGI contacting you by telephone regarding recruitment services, market updates, and relevant business opportunities
We believe in equal opportunity for all and actively encourage applications from diverse backgrounds, experiences, and perspectives.
Source Group International Ltd is acting as an Employment Business in relation to this vacancy