The Project (CQV) Engineer role involves conducting Commissioning, Qualification, and Validation activities in the life sciences sector, focusing on safety and project timelines. Responsibilities include generating C&Q procedures, writing and reviewing qualification documents, coordinating project resources, and conducting design reviews and equipment testing.

The Process Engineer will design and specify cGMP process equipment, manage small-to-medium scale projects, support QA Validation, revise process diagrams, investigate equipment issues, and implement improvements. This role emphasizes compliance, safety, and readiness for tech transfer activities.