Senior 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 high knowledge of process equipment’s systems Should have knowledge on terminologies of symbols used in PID. Execute C Q activities with multiple stakeholders like (Engineering responsible, Design consultant, Vendor’s, and QA) of the project organization 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. Generate validation deliverables like IQ, OQ, PQ protocols and reports, etc. Act as Smarter Execution consultant for Project Members. Ensure C Q documentation is in compliance with GMP and GEP (incl. ASTM E2500). Conduct follow-up on QAP planned C Q activities