Validation Engineer

CAIIndia

On-site Full-time

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Experience Level

Experience

Qualifications

Key Responsibilities: • Develop and implement Commissioning, Qualification, and Validation (CQV/CSV) protocols and plans for pharmaceutical facilities and systems.• Assist in the creation of Commissioning and Qualification (C&Q) procedures for client projects.• Collaborate with cross-functional teams to ensure compliance with regulatory standards.• Maintain comprehensive documentation and reports to support validation processes.

About the job

About CAI:

Founded in 1996, CAI has evolved into a global leader with over 750 professionals dedicated to delivering exceptional commissioning, qualification, validation, start-up, project management, and consulting services tailored for FDA-regulated and mission-critical sectors.

Are You Ready to Make a Difference?

At CAI, we prioritize our clients, ensuring that we leave no stone unturned until we achieve the desired outcomes. Our commitment to excellence drives us to go above and beyond, ensuring operational readiness for our clients.

We embody our Foundational Principles in every aspect of our work:

• Integrity in all actions

• Commitment to serving each other and our communities

• Focus on long-term sustainability and growth

We believe that the success of one is the success of all. By fostering a collaborative environment, we ensure that teamwork, respect, and a proactive attitude are at the core of our culture, enabling our remarkable growth.

About CAI

CAI is a leading global provider of operational readiness solutions, specializing in commissioning, qualification, validation, and project management for industries regulated by the FDA and other critical sectors. With a strong commitment to client success and integrity, CAI has built a reputation for excellence in delivering innovative solutions that drive operational efficiency.

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