Engineering

As a hands-on CQV Engineer, you will be an integral part of a project team, overseeing the commissioning, qualification, and validation of GMP facilities, process equipment, and critical building and utility systems within our client’s life sciences production facility. This role encompasses the design, implementation, and documentation of these qualifications, along with their life-cycle management, ensuring compliance with all applicable regulatory and internal quality standards (FDA and/or EU regulations).

As a CSV Specialist, you will be responsible for testing and qualifying process installations and equipment. Additionally, you will organize and oversee testing and qualification/validation activities, acting as the point of contact for relevant departments (such as Production, QA/QC).
Do you have experience with qualification projects? Have you worked within a GMP, GLP, GDP or ISO 13485 environment? If so, please read on!

As a Project Engineer, you will leverage your strong soft skills and broad technical expertise to oversee projects from design through implementation to testing and validation. Coordination and communication are crucial, as you will collaborate with professionals from various departments to guide projects to successful completion.
Projects typically involve equipment (filling, sterilization, freeze dryers, etc.), pharmaceutical buildings, cleanrooms (building, HVAC, utilities), and more.