We have an exciting opportunity for a Validation and Qualification Engineer (m/f/d) in Switzerland
Tasks
- You execute site projects related to Qualification Cleaning/Sterilization Validation.
- You support the development review and improvement of Qualification Cleaning/Sterilization Validation documentation such as SOPs and reports.
- You support the evaluation of innovative equipment/technologies with respect to Qualification and Cleaning/Sterilization Validation reviewing user requirements.
- You support the implementation of process changes and root cause investigation of deviations.
- You act as a deputy point of contact for Qualification and Cleaning/Sterilization Validation.
Requirements
- You have a university degree preferably in Engineering Biotechnology Biology or Microbiology.
- You have a good understanding of current GMP regulations and industrial standards.
- You have experience in auditing and compliance within the pharmaceutical industry which is preferred.
- You have experience in change and deviation management.
- You have strong project management skills.
- You can define and lead projects to support improvement implementation or remediation.
- You have strong communication skills planning and delivering ideas and information to others in a clear and impactful manner.
Thank you for considering this opportunity. I look forward to connecting with you.