Cleaning Validation Engineers,Glendale, CA (On-Site)
Dice is the leading career destination for tech experts at every stage of their careers. Our client, Algo Soft Solutions LLC, is seeking the following. Apply via Dice today!Job Title: Cleaning Validation EngineersIndustry: BiotechnologyLevel of Experience: 4+ yearsLocation: Glendale, CA (On-Site)Duration: Through the end of the year + (Initial Contract)Responsibilities Develop and execute cleaning validation protocols, reports, and risk assessments in accordance with cGMP, FDA, EMA, and other regulatory guidelines. Establish scientifically justified acceptance criteria for residues and cleaning limits. Perform and document visual inspection assessments and residue sampling (swab and rinse methods). Coordinate validation activities with Manufacturing and QA to ensure proper execution during production campaigns. Analyze laboratory data for residuals testing and interpret results to determine cleaning process effectiveness. Investigate cleaning failures, deviations, and nonconformities; implement corrective and preventive actions (CAPAs). Partner with Engineering and Operations to optimize cleaning processes and support new equipment commissioning. Support change control activities related to equipment modifications, new product introductions, or updated cleaning procedures. Write and maintain SOPs related to cleaning validation and verification programs. Ensure documentation meets global regulatory expectations, internal quality standards, and audit readiness.Requirements Bachelor’s degree or higher in engineering, Chemistry, Pharmaceutical Sciences, or a related scientific field. 4+ years of experience in the Biotechnology or Pharmaceutical industries Strong knowledge and experience implementing cleaning validation principles (MACO calculations, PDE-based limits, swab/rinse recovery studies). Strong technical writing and protocol/report development skills. Ability to analyze complex data and troubleshoot validation issues. Effective communication and cross-functional collaboration skills. Proficiency with validation lifecycle management systems and quality management systems (TrackWise, Kneat, Veeva, etc., a plus).