Senior Project Engineer (m/f/d) Automation

Would you like to contribute your expertise in automation technology in an exciting environment in Heidelberg?

As an experienced project engineer, you will support the team on site in the planning and maintenance of highly complex systems.

In this permanent position, you will drive innovative solutions and make a direct contribution to process reliability. We place great value on equal opportunities and look forward to receiving your application. Impress us with your profile and apply today to Randstad for direct placement!

Here's what our clients offer

• Direct placement into a permanent employment contract
• Option for mobile working after the training phase
• Collaboration in an experienced and dynamic team of 17 colleagues
• Challenging work environment with state-of-the-art manufacturing technologies
• Individual support and excellent development prospects

Your tasks

• Maintenance, support and targeted further development of automation systems for state-of-the-art bioprocess plants
• Support in the planning (engineering) of new production facilities as well as in modifications and upgrades of existing process lines
• Monitoring and active troubleshooting of industrial communication systems
• Ensuring data integrity, network stability, segmentation and security standards in close cooperation with the IT department.
• Participation in plant qualification and validation to ensure strict GMP compliance
• Thorough, GMP-compliant documentation of changes, malfunctions and maintenance, as well as technical support during internal and external audits.
• Communication with plant suppliers and service providers, as well as regular training of users from production, engineering and quality control.

Your profile

• Successfully completed studies in electrical engineering, automation engineering, process engineering, mechatronics or a comparable qualification
• Senior-level professional experience and project experience are mandatory in the GxP-regulated environment of a CDMO or in the pharmaceutical/biotech industry.
• Practical knowledge in the qualification/validation of GMP facilities (CSV/CSA, 21 CFR Part 11, EUR Annex 11 etc.)
• Solid knowledge of SIMATIC PCS 7 , TIA Portal and WinCC/SCADA systems
• Ideally, you have user knowledge of Unicorn software (Cytiva) and AVEVA PI.
• Basic understanding of network architectures and industrial communication
• Hands-on mentality, analytical thinking, team spirit, and a strong sense of responsibility and quality awareness.
• Excellent German and English skills, both spoken and written.