CQV Lead

Job Summary

We are seeking a CQV Lead (OSD Manufacturing) with strong engineering fundamentals and hands-on experience in commissioning, qualification, and validation within a GMP-regulated Oral Solid Dose (OSD) environment. This role involves leading end-to-end CQV activities for manufacturing equipment, packaging systems, utilities, facilities, and computerized systems.

Roles & Responsibilities

• CQV Leadership & Execution:
  • Lead commissioning, qualification, and validation (CQV) activities for OSD manufacturing and packaging systems
  • Develop and execute risk-based IQ/OQ/PQ protocols aligned with critical quality attributes (CQAs) and critical process parameters (CPPs)
  • Translate URS, FS/DS, and design specifications into testable acceptance criteria
  • Evaluate system performance, operational ranges, and process reliability
• Digital Validation & Documentation:
  • Utilize digital tools and structured templates to efficiently generate validation documentation (protocols, reports, RTMs)
  • Perform thorough technical review and approval of all validation deliverables
  • Ensure compliance with data integrity principles (ALCOA+) and Good Documentation Practices (GDP)
  • Maintain inspection-ready documentation at all times
• Lifecycle & Compliance Management:
  • Maintain validated state through lifecycle management, periodic reviews, and requalification activities
  • Lead/support change controls, deviation investigations, and CAPA implementation
  • Ensure compliance with cGMP, FDA regulations, and 21 CFR Part 11 requirements
• Technical Problem Solving:
  • Identify critical parameters, control strategies, and challenge system design assumptions
  • Troubleshoot issues related to equipment, utilities, and automation systems (PLC/SCADA, data historians)
• Cross-Functional Collaboration:
  • Partner with QA, MS&T, Automation, and Manufacturing teams for project execution and compliance readiness
  • Communicate technical risks, timelines, and decisions effectively

Education & Experience

• Master's or PhD in Engineering (Chemical, Mechanical, Electrical, Industrial, Automation, or related field) with 3+ years of relevant experience
• Hands-on CQV experience in a GMP-regulated Oral Solid Dose (OSD) manufacturing and/or packaging environment
• Proven experience in authoring and executing IQ/OQ/PQ protocols and validation reports
• Experience with Computerized System Validation (CSV), data integrity, and 21 CFR Part 11 compliance
• Strong understanding of OSD unit operations such as blending, granulation, compression, coating, and encapsulation
• Familiarity with automation systems (PLC/SCADA) and data historians (e.g., PI)
• Ability to interpret mechanical, electrical, and control system designs
• Excellent technical writing, analytical, and problem-solving skills
• Experience using digital validation tools and structured documentation systems is preferred