Commissioning & Validation Engineer (12 Months
1 week ago
**About CAI**
CAI provides commissioning, qualification, validation, start-up, project management and consulting services related to operational readiness to FDA regulated and other mission critical industries.
**Meeting a Higher Standard**
Our approach is simple; we put the client’s interests first, we do not stop until it is right, and we will do whatever it takes to get there.
As owners of CAI, we are committed to living our Foundational Principles, both professionally and personally:
We act with integrity
We serve each other
We serve society
We work for our future
We work diligently to accomplish team goals. We place Team Before Self, demonstrate Respect for Others, and possess a can-do attitude. That is how we have grown exponentially.
**The Role**:
**Requirements include**:
Position Description:
The CQV Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment. These people are responsible for protocol writing and execution (field verification), and development of summary reports at client sites.
Position Requirements:
BS or MS in a relevant science or engineering field, or equivalent
Minimum 5 years of industrial/relevant experience in the Pharmaceutical/Biotechnology
Excellent technical problem-solving and basic troubleshooting skills.
Experienced in commissioning of equipment
High attention to detail.
Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines.
Ability to work independently, while supporting other team members.
Proficiency in Microsoft Word and Excel
Familiarity with mechanical, electrical, and automation / control systems a plus.
Other Requirements:
Excellent oral and written English is required
Able to travel domestically and internationally if required
LI-KO1
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