Visp
12 months
41 hours
SL-000631
SL-000631
About the client
- 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
