In this role, you will contribute to automation projects within a dynamic life sciences environment. You will develop specifications, support system testing, and lead automation change activities. Your work will help optimize manufacturing processes and ensure compliance with quality standards.

Start Date: 01/10/2025

Duration: 12 Months

Place of Work: Visp

Key Responsibilities

  • Create and update automation system specifications
  • Conduct offline and online coding, testing, and peer reviews
  • Manage the design, development, and documentation of Automation Change Records (ACRs) and related validation activities
  • Lead automation aspects of unit operations, resolving issues efficiently and implementing changes on complex projects
  • Evaluate proposed modifications and investigate discrepancies during manufacturing
  • Troubleshoot equipment, process, and system failures
  • Assist in developing policies and standards for automation practices at the site
  • Introduce innovative automation solutions to enhance quality and productivity

Candidate Profile

  • Proven experience with automation systems, particularly in manufacturing contexts
  • Strong knowledge of automation control systems, such as DeltaV or MES PharmaSuite
  • Excellent problem-solving and troubleshooting skills
  • Good communication skills and team collaboration abilities
  • Fluent in business English

 

Job ID 41181159