Description

In this role, you will engage in a variety of tasks, including representing the QC Microbiology department in audits and developing and verifying analytical methods. Your contributions will help ensure compliance and drive continuous improvements in quality control processes.

Requirements

• •MSc or PhD in Microbiology, Biology, Pharmaceutical Sciences, or equivalent experience
• •Proven work experience in pharmaceutical Quality Control, particularly with endotoxin and/or bioburden analysis
• •GMP knowledge
• •Organizational skills and ability to manage multiple tasks
• •Proficiency in English; German language skills advantageous

Tasks

• •Represent the QC Microbiology department at meetings and audits
• •Serve as the scientific SME for project-specific microbial analyses
• •Monitor and evaluate current improvements in QC Microbiology
• •Coordinate work package completion within business units
• •Ensure timely communication among interdisciplinary teams
• •Collect and evaluate verification data to identify weak points
• •Implement corrective measures for flawless operations
• •Define cGMP examinations for deviations to ensure compliance
• •Participate in creating and releasing technical documentation
• •Develop verification plans and reports
• •Develop and verify analytical microbiology methods
• •Support other departments with Quality Assurance tasks
• •Contribute to various projects at the Visp site
• •Drive process improvements to maintain competitive edge
• •Be on-call approximately 3-4 times per year

Benefits