At Compleat Technical Solutions INC, we specialize in providing comprehensive workforce solutions tailored to the needs of the biotechnology, pharmaceutical, medical device, and IT industries. With expertise in recruitment for Quality, Validation, Regulatory Affairs, and IT, we are dedicated to supporting life science companies throughout the entire CQV (Commissioning, Qualification, and Validation) lifecycle. Our team of professionals excels in delivering Validation support across various areas including CQV/Equipment Validation, Process Validation, Cleaning Validation, Computer Systems Validation, Analytical Lab Equipment Validation, Calibration, Preventive Maintenance, and Regulatory Affairs. We understand the critical importance of compliance and efficiency in highly regulated industries, and our services are designed to ensure adherence to industry standards and regulations. Here's what we specialize in: ✅ Facilities Equipment ✅ Utilities Equipment ✅ Processes ✅ Cleaning Validation ✅ Test Method Validation ✅ Greenfield CQV Projects ✅ New Production Suite Commissioning ✅ Decommissioning ✅ End-to-End Solutions ✅ Project Planning ✅ Validation Master Plans (VMP) ✅ User Requirements Specifications (URS) ✅ Risk Assessments ✅ Protocols (FAT, SAT, etc.) ✅ Summary Reports ✅ Traceability Matrix ✅ Calibration Matrix ✅ SOPs ✅ Integrated Commissioning and Qualification (ICQ) ✅ Validation Protocol Format ✅ Design Qualification (DQ) ✅ Installation Qualification (IQ) ✅ Operational Qualification (OQ) ✅ Performance Qualification (PQ) ✅ Good Automated Manufacturing Practice (GAMP) ✅ Current Good Manufacturing Practice (cGMP) Review ✅ Continued Process Verification (CPV) ✅ Pre-Operational Verifications ✅ Commissioning and Startup ✅ Technical Audits and Due Diligence Connect with us today to learn more about how we can elevate your operations and drive excellence in quality, validation, and regulatory compliance!
