Validation Engineer

We are seeking a CQV Engineer to develop documentation for Commissioning, Qualifications, and Validation in Italy. The role involves protocol writing, execution, and development of summary reports at client sites.

Requirements

• High attention to detail
• Ability to multi-task and take initiative
• Bachelor's or Master's degree in a relevant science or engineering field
• 4-8 years of experience in commissioning and qualification activities in an FDA regulated industry
• Excellent technical problem-solving and troubleshooting skills
• Ability to work independently and manage project teams
• Proficient in life science manufacturing processes
• Expertise in Microsoft Word and Excel

Benefits

• Competitive salary
• Opportunities for career growth and professional development
• Collaborative and dynamic work environment