QA Validation Specialist 3

Equipment Validation AnalystRole is Equipment Validation and Cleaning ValidationExperience with Kneat is absolutely required. Experience with Ellab for Temp Mapping is a plusManager is looking for candidates with Cleaning Val (CIP, COP, SIP). 95% of equipment is single-use, so the Cleaning Val is limited mostly to Media Hold/Media Fill. Cleaning Val is mostly drafting SOPsOther equipment includes Autoclaves, Parts Washers, and Storage equipment (cold and ambient). Looking for a worker to Build Equipment Requalifications in Kneat.Job Description:Provide Subject Matter Expert support to Quality Control, Manufacturing, and other departments for the design, operation, and troubleshooting of equipment.Drive/own the validation plans and execution of equipment changes and process improvements.Execution of Installation Qualifications/Operational Qualifications and drafting of Performance Qualifications as required.Perform Equipment Validation activities to include Validation Maintenance Quality Systems review, and requalification to ensure GMP equipment is continuously maintained in a validated state.Program, organize, and maintain Validation equipment and supplies, including dataloggers and probes.Demonstrate a general understanding of biopharmaceutical manufacturing equipment and validation procedures for Installation Verification (IV/IQ), Clean-In-Place (CIP), Steam-In-Place (SIP), Autoclaves, Clean Utilities, Shipping Validation, Temperature Mapping, Controlled Storage Rooms and Equipment.Develop validation protocols from plans and engineering documents.Provide basic technical support when reviewing and approving SOPs, Protocols, Change Controls, Deviations, CAPA, etc.Perform assigned Quality Systems activities within the Document Management System (DMS), TrackWise Quality System (Change Control, Deviation, CAPA)Perform other duties as assigned.