PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, employing a global team of skilled professional and experts that span across strategically located offices in the United States, Europe, Asia, and the Middle East. PSC operates in 52 countries globally and has served thousands of clients to date. We focus on providing quality consulting services to ensure our clients success. PSC provides cost-effective solutions, while providing exceptional technical capabilities and customer service to our clients for all projects ranging from supplier quality audits to greenfield projects. We understand that the world of life science is evolving rapidly, and we must continue to offer new products and services to meet our customers expectations. We are looking for a CQV Engineer to join our team. Responsibilities: GMP Assistance at Plant. Formulation System Reset. Filling/Packaging/Warehouse System Reset. Validation System Reset. System updates (QSF/SOP/Forms). Training on new updates. Requirements Five to 10 years experience in Pharma. Industry specific technical knowledge. Experience with QA measuring and testing equipment in pharmaceuticals Experience with Change Management. Knowledge and experience with GMP. Experience in Engineering. Experience with Equipment Qualification/Validation, Facilities Qualification/Validation, andQC Lab Instruments Qualification/Validation. Experience with Installation Qualification (IQ),Operational Qualification (OQ), andPerformance Qualification (PQ). Revising and creating Standard Operating Procedure (SOP). Experience with Validation Plan (VP),Validation Risk Assessment, andValidation Summary Report (VSR).