Hiring: Engineer, Validation Company: Voyant Beauty Location: Johnstown, OH Job Posted Time: 2026-09-11 10:40:44 Target Skills & Keywords : Microsoft Excel, Microsoft Office, Quality Assurance, Root Cause Analysis, Six Sigma About the job Experience: •1-3 years in validation within a cGMP manufacturing environment (preferably cosmetics, pharmaceutical, Or Personal Care). (Preferred) •1-3 years in calibrating, testing, and validating instrumentation, mechanics, and computer systems. •3 years in validation within a cGMP manufacturing environment (preferably cosmetics, pharmaceutical, Or Personal Care). (Preferred) •3 years in calibrating, testing, and validating instrumentation, mechanics, and computer systems. Required Skills: •Review and approve validation protocols (IQ/OQ/PQ) for equipment, manufacturing processes, and cleaning procedures. Develop template protocols, interim, and review final reports for new and existing systems, including USP water and compressed air systems. •Write, review, and maintain SOPs, validation protocols, and technical documentation to ensure audit readiness and consistency. Develop standards and templates for custom and regulated products. •Controlled systems. Assist in the creation of cleanout SOPs and perform engineering testing as needed. •Participate in internal and external audits. Maintain validation documentation for inspections and provide subject matter expertise on cGMP activities. •Attend customer and cross-departmental meetings. Support departments with technical insight on validation and compliance-related concerns. •Assist with environmental monitoring activities and interface with 3rd party labs. Review analytical and microbial test results and methods •Provide input into equipment purchase decisions with validation requirements in mind. •Support quality investigations and deviations related to validation or equipment failures. Qualifications: •Bachelor's Degree in Mechanical Engineering, Chemical Engineering (Required) or related technical field. () •Process, cleaning, equipment, and utility validation (High proficiency) •IQ/OQ/PQ protocol development and execution (High proficiency) •CGMP compliance and regulatory standards (High proficiency) •Analytical and microbiological test interpretation (Medium proficiency) •SOP and technical document writing (High proficiency) •Cross-functional collaboration and stakeholder communication (High proficiency) •Root cause analysis and deviation support (Medium proficiency) •Environmental monitoring and lab coordination (Medium proficiency) •Equipment and computer system qualification (High proficiency) Interested candidates, please apply directly through the job posting on company's career page or try via AI auto apply on this platform. Don't miss this opportunity to join a forward-thinking team!