CQV Engineer

1 mese fa

Roma, Lazio, Italia Cai A tempo pieno
Job Title: CQV Engineer

We are seeking a highly skilled CQV Engineer to join our team at Cai in Italy. The successful candidate will be responsible for developing documentation to support Commissioning, Qualifications, and Validation activities.

Key Responsibilities:
  • Develop and execute protocol writing and execution, field verification, and development of summary reports at client sites.
  • Support documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
  • Provide cGMP leadership and guidance for the integration and delivery of CQV services for our Life Sciences clients.
Requirements:
  • High attention to detail.
  • Ability to multi-task and take initiative to accomplish assigned tasks accurately.
  • Minimum 4 – 8 years' experience performing commissioning and/or qualification activities in an FDA regulated industry.
  • Excellent technical problem-solving and troubleshooting skills, with solid knowledge of typical project technical issues.
Preferred Skills:
  • Isolators qualification protocols execution and reporting.
  • VHP cycle development.
  • GMP based knowledge.
  • Expertise in Microsoft Word and Excel.
What We Offer:
  • Opportunity to work with a dynamic team at Cai.
  • Chance to develop your skills and expertise in CQV.
  • Competitive salary and benefits package.

  • CQV Engineer

    2 settimane fa

    Roma, Italia CAI A tempo pieno

    We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and development of summary reports at the client site. The role of a CQV Engineer in CAI is to: ...