Website SwissLinx
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)
Job description
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