Take your career to the next level with Amaris Consulting as a MES System Engineer (Pharma).
Be part of an international team, thrive in a general group with a €800M turnover and over 1,000 clients worldwide, and an agile environment. The idóneo candidate will have a proven track record in building scalable, high-quality applications and is comfortable working across the entire stack.
✍️ WHAT WOULD YOU NEED? ✍️
- 3+ years of experience working with Manufacturing Execution Systems (MES), preferably Körber PAS-X or similar platforms
- Strong experience working with Windows and Linux operating systems
- Solid knowledge of relational databases such as Oracle Database and PostgreSQL
- Experience supporting and maintaining applications in production environments
- Good understanding of GxP / GMP regulated environments and compliance requirements
- Experience with system monitoring, troubleshooting, and performance optimization
- Ability to manage change requests, testing, documentation, and deployments
- Experience collaborating with IT and OT teams in industrial or manufacturing environments
- Familiarity with virtualization tools such as Citrix is a plus
- Knowledge of container technologies such as Docker and/or Kubernetes is a plus
- Fluent English required
WHAT WILL YOU BE DOING?
- Support and ensure the smooth operation of MES applications and their technical environments
- Manage daily operations, incidents, and service requests related to MES platforms
- Coordinate and implement application and infrastructure changes, including testing and documentation
- Monitor system performance, capacity, and reliability, proposing improvements where needed
- Ensure compliance with GxP standards, including audit support and validation activities
- Perform and coordinate technical operations such as backups, disaster recovery testing, patching, and upgrades
- Manage user access, security controls, and system integrity (CIA: Confidentiality, Integrity, Availability)
- Collaborate closely with IT, OT, and business teams to support manufacturing processes
- Maintain accurate documentation and ensure traceability of all system changes
- Contribute to continuous improvement initiatives related to system reliability, performance, and operational excellence