Advanced CQV Engineer

Would like to help making complex biopharma facilities more sustainable. Driving the project with Science and Risk based Validation (SRV) concept. Work very closely with our customers. Have knowledge of commissioning of Process Utility systems and collaborate with multi-discipline teams to integrate piping distribution, instrumentation and automation services, facilitate and ensure right commissioning across the project. Good technical knowledge on Piping codes and standards. Should have knowledge on terminologies of symbols used in PID. Perform C Q activities in smaller cross-disciplinary teams: Align quality and validation concept with customer’s quality system validation concept Define scope of C Q activities in project and scope of work within quality work package incl. relevant C Q activities Ensure changes to scope are brought to the attention of Project Management. Ensure interfaces to and coordination with other disciplines and compliance with codes, regulations and relevant Procedures. Ensure right level of commissioning processes so as to have smooth qualification phases Generate validation deliverables like commissioning , protocols etc Ensure C Q documentation is in compliance with GMP and GEP (incl. ASTM E2500). Conduct follow-up on QAP planned C Q activities