CQV Engineer Bologna
3 settimane fa
We are seeking a highly skilled CQV Engineer to join our team in Bologna, Italy. The successful candidate will be responsible for developing documentation to support Commissioning, Qualifications, and Validation activities.
Key Responsibilities:- Develop and execute protocols for Commissioning, Qualification, and Validation activities
- Support the development of summary reports at client sites
- Collaborate with cross-functional teams to ensure compliance with regulatory requirements
- Provide technical guidance and leadership on CQV services for Life Sciences clients
- Ensure high-quality documentation and execution of CQV activities
- BS or MS in a relevant science or engineering field, or equivalent years of experience
- Minimum 4-8 years' experience in Commissioning and/or Qualification activities in an FDA-regulated industry
- Excellent technical problem-solving and troubleshooting skills
- Strong attention to detail and ability to multi-task
- Proficient in life science manufacturing processes and equipment
- Excellent oral and written English skills
- Opportunity to work with a leading company in the Life Sciences industry
- Collaborative and dynamic work environment
- Professional development and growth opportunities
We are an equal opportunities employer and welcome applications from diverse candidates. Please note that the selection process respects the principle of equal opportunities (L. 903/77). #LI-AG1
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