Cleaning Validation Specialist
ACL Digital
Job Title Validation Engineer/Cleaning Validation Specialist I Location Holly Springs, NC Duration 1 year contract Description Cleaning Validation Specialist I Ideal Candidate 5+ YOE with a B.S. in Science, Engineering, and Pharmacy areas. Standard Hours Hours may vary to support manufacturing (early/later shifts, possible weekends). Top Must Have Skill Sets Proficient with KNEAT or similar programs. Strong understanding of GMPs and global regulatory expectations. Ability to interpret equipment design, P&IDs, and process flow diagrams. Excellent technical writing and documentation skills. Strong analytical and problem solving abilities.Effective communication and cross-functional collaboration. Ability to work independently and manage multiple priorities. Nice to have Project management experience. Job Description Coordinate cleaning validation activities. Prepare and execute protocols and reports for cleaning development and validation. Perform investigation of deviations / discrepancies. Support authoring and executing CV/CHT/SHT protocols, progress package work and wrap up executed studies. Supports non-traditional work schedule based on project and business needs. Familiar with Drug substance process equipment, autoclaves, parts washers, CIP skids to support CV program. Demonstrated proficiency in utilizing PI for run trending analysis and facilitating favorable completion of support packages. Leads and performs on floor CV execution and sampling. Provide technical support and sample management to cleaning activities associated with the manufacturing process. Proficient with KNEAT execution. Design and develop cleaning procedures for new products and manufacturing equipment. Investigates and conducts troubleshooting/root cause analysis of cleaning related incidents, deviations and cleaning out of specification results for non-validated or under development cleaning procedures. Supports the periodic review of cleaning validation studies. Performs successful and on time resolution of incidents and deviations related to cleaning validation exercises. Collaborate with cross-functional teams, including Quality Assurance, Manufacturing, and Engineering, to ensure cleaning validation activities are integrated into the overall project plan. Trains manufacturing and QC/QA personnel on cleaning validation documentation. Basic Qualifications Master degree or Bachelor degree and 2 years of experience or Associate degree and 6 years of experience or high school diploma / GED and 8 years of experience #J-18808-Ljbffr
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