Cleaning Validation Consultant

Contract: 12-month Contract (2-3+ year scope) Onsite Requirement: Hybrid Overview We are supporting a large-scale biologics manufacturing facility undergoing significant capacity expansion in the North Carolina life sciences corridor, and are seeking an experienced Cleaning Validation Consultant to lead cleaning validation activities across multiple manufacturing suites ahead of a major regulatory inspection window. This role exists to ensure cleaning processes for both single-use and reusable equipment trains are robust, scientifically justified and fully documented as the site scales production. You will author and execute cleaning validation protocols, manage residue and analytical limits, and partner closely with Quality and Manufacturing to keep the site inspection-ready throughout a period of rapid growth. Key Responsibilities Author, execute and report cleaning validation protocols (IQ/OQ/PQ) for process and equipment cleaning across new and existing manufacturing trains Develop residue limits and acceptance criteria based on toxicological data, MACO calculations and risk assessment Partner with Analytical/QC teams to qualify swab and rinse sampling methods and review analytical recovery data Investigate and resolve cleaning validation deviations, including root cause analysis and CAPA development Maintain the site cleaning validation master plan and ensure ongoing state of control through periodic verification Support tech transfer and new product introduction activities by assessing cleaning impact and updating validation strategy Liaise with Quality Assurance to ensure all documentation meets cGMP standards and is inspection-ready Provide SME support during regulatory inspections and client audits on cleaning validation matters Required Experience 6–10+ years in cleaning validation within a GMP pharmaceutical, biotech or CDMO environment Demonstrable experience authoring and executing cleaning validation protocols from a risk-based, data-driven approach Strong working knowledge of MACO/PDE-based limit setting and current regulatory expectations (FDA, EMA, PIC/S) Experience qualifying and interpreting swab/rinse recovery and analytical testing data Bachelor\'s degree in Chemistry, Chemical Engineering, Microbiology or related scientific discipline Preferred Experience Experience in large molecule / biologics manufacturing (mAbs, cell or gene therapy) Track record supporting cleaning validation through a facility expansion or new suite start-up Experience preparing cleaning validation documentation for FDA PAI or pre-approval inspections Familiarity with shared-equipment trains and multi-product facility cleaning strategies Comfortable operating independently and managing competing protocol timelines in a fast-paced GMP environment #J-18808-Ljbffr i-Pharm GxP