* Duration: ASAP - 12 months with potential extension
* Workload: 100% (two positions)
* Language: English (business fluent), German a plus
* Environment: cGMP/GxP manufacturing, automation projects (tech transfers, new technology introductions)
You will be working with the Automation team on projects such as tech transfers and new technology introductions.
Requirements
* Develop and update automation-related specifications
* Perform off-line and on-line coding, testing, and peer reviewing
* Own the design, development, and execution of Automation Change Records (ACRs), Quality Change Records, and control qualification/commissioning test documentation
* Serve as the automation lead for unit operations, driving efficient issue resolution and change implementation on large/complex projects
* Assess proposed changes and evaluate discrepancies during manufacturing operations
* Troubleshoot process, equipment, and system malfunctions or failures
* Contribute to the development of policies and standards for the Automation field at the site
* Implement new approaches within Automation to improve quality and efficiency
Competences
* Degree in Engineering, Automation, Life Sciences, or related field
* 3+ years of experience in a regulated GMP environment (pharma/biotech preferred)
* Strong knowledge/experience with either DeltaV (Position 1) or MES PharmaSuite (Position 2)
* Experience in automation coding, testing, and documentation within GMP/GxP environments
* Familiarity with change control processes (e.g., ACRs, Quality Change Records) and commissioning/qualification activities
* Strong troubleshooting skills for process, equipment, and system issues
* Excellent coordination, documentation, and communication skills
Maybe not for you, but for someone else?
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