Senior Cqv Engineer

PPD (Thermo Fisher)

Switzerland
Bachelor's degree in biotechnology or engineering
10 years experience in engineering field
Experience in pharmaceutical qualification and validation
Join a world-class company committed to making the world healthier, cleaner, and safer through collaboration and innovation

Job Summary

  • Join a world-class company committed to making the world healthier, cleaner, and safer through collaboration and innovation.
  • The role involves defining requalification strategies for GMP systems and coordinating execution with external contractors.
  • Candidates must prepare, review, and approve production, validation, and audit reports while adhering to strict safety standards.

Matching Summary

Join a world-class company committed to making the world healthier, cleaner, and safer through collaboration and innovation.

Skills & Requirements

Must-have

  • Bachelor's degree in Biotechnology or Engineering
  • 10 years experience in engineering field
  • Experience in pharmaceutical qualification and validation
  • Functional knowledge of cGMPs and FDA regulations
  • Proficiency in electronic documentation systems like TrackWise

Nice-to-have

  • Excellent verbal and written communication skills
  • Experience with multi-cultural work environment
  • Certification in technical writing or quality management
  • Fluency in German or another European language
  • Strong understanding of continuous improvement culture

Key Requirements

  • Bachelor's degree + 10 years experience OR Master's + 3 years
  • Required experience in pharmaceutical industry for qualification & validation
  • Strong technical writing skills with attention to detail
  • Proficiency in MS Office and electronic documentation management systems

Work Rights

Not specified

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