Process Validation Engineer

Responsibilities: Lead migration of legacy documents into Kneat digital platform, ensuring compliance and consistency. Qualify redundant lab equipment (e.g., pH meters, thermal mixers, peristaltic pumps, nutating mixers) to ensure operational integrity. Perform equipment and temperature mapping studies, particularly for Ellab systems, based on project needs. Support Process Engineers by filling resource gaps, ensuring projects remain on track during critical milestones. Document and support Comp

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined

Are You Ready? CAI is a professional services company established in 1996 that has grown to more than 700 people worldwide. We provide commissioning, qualification, validation, startup, project management, and other consulting services associated with operational readiness to FDA-regulated and other mission-critical industries. Our approach is simple-we put the client's interests first, we don't stop until it's right, and we do whatever it takes to get there. Our Foundational Principles: - W

Job Title: Senior CQV Engineer/Manager Location: Remote / Hybrid / Onsite (Depending on Project Requirements) Duration: Long-Term Contract Position Overview We are seeking an experienced CQV (Commissioning, Qualification & Validation) professional to support and lead validation activities within highly regulated pharmaceutical, biotechnology, and life sciences environments. This role will be responsible for ensuring GMP compliance across facilities, utilities, equipment, manufacturing processes,