Search the 2 jobs at CAI

The Process Engineer will design and specify cGMP process equipment, manage small-to-medium scale projects, participate in design reviews, and support QA Validation. Responsibilities also include revising diagrams, investigating control system issues, implementing process improvements, and ensuring compliance with relevant laws.

The Qualified Person (QP) is responsible for certifying medicinal products, providing quality and compliance guidance, overseeing documentation processes, supporting audits, and maintaining industry legislation knowledge. They will also support continuous improvement initiatives and collaborate within cross-functional teams.