CQV Engineer

PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America, Europe, Asia and the Middle East, we are proud of the roles we have fulfilled to help our clients achieve success. The Experience With operations spanning the globe and featuring a multi-cultural team, PSC Biotech® is passionate about bringing the best and brightest together in an effort to form something truly special. When you decide join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents. We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn. At PSC Biotech®, it’s about more than just a job—it’s about your career and your future. Your Role We are seeking CQV Engineers of varying experience levels to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and manufacturing systems within regulated life sciences environments. The CQV Engineer will play a critical role in ensuring systems are designed, installed, tested, and operated in compliance with cGMP requirements, industry standards, and client expectations. Successful candidates will collaborate with engineering, quality, manufacturing, and project teams to deliver compliant and efficient validation solutions. Develop, review, and execute commissioning, qualification, and validation documentation for facilities, utilities, equipment, and manufacturing systems. Author and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Support commissioning activities including system walkdowns, punch-list resolution, turnover packages, and startup support. Perform equipment and utility qualification activities for systems such as HVAC, clean steam, purified water, WFI, compressed gases, CIP/SIP systems, process equipment, and cleanroom environments. Support development of validation plans, risk assessments, traceability matrices, and final reports. Participate in discrepancy investigations, deviation resolution, CAPA activities, and change control assessments. Coordinate with cross-functional stakeholders including Engineering, Manufacturing, Quality Assurance, Automation, and Facilities. Review design documentation, specifications, P&IDs, and engineering packages to ensure qualification readiness.…