CQV Engineers (Multiple Levels)

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 and Validation Engineers at multiple experience levels to support pharmaceutical and biotechnology manufacturing projects involving facility, utility, equipment, automation, and process validation activities. These positions will play a key role in commissioning, qualification, and validation efforts associated with manufacturing expansions, new product introductions, capital projects, and operational readiness initiatives within regulated GMP environments. Successful candidates will contribute to protocol development, field execution, discrepancy resolution, and documentation activities while working closely with engineering, quality, manufacturing, automation, and project teams. Opportunities are available for entry-level through senior-level professionals, with responsibilities scaled according to experience and technical expertise. Candidates must have prior experience working within Kneat Gx. Validation Execution & Documentation Author, review, execute, and close commissioning, qualification, and validation protocols and reports. Support installation, operational, and performance verification activities for facilities, utilities, equipment, and manufacturing systems. Execute field testing and document results in accordance with established quality and documentation standards. Assist with protocol revisions, data analysis, and final report generation. Maintain traceability between requirements, risk assessments, testing activities, and validation deliverables. Project Support Coordinate with project engineers, manufacturing personnel, quality representatives, automation engineers, and vendors…