Quality Assurance Technician
7 days ago
Orangeburg
Job Description Job Title: Quality Assurance Technician Book for immediate interests: have QA experience within GMP environment Job Description: As a Quality Assurance Technician, you will perform daily inspections of all production lines to ensure compliance with Good Manufacturing Practices (GMPs) and company standards. You will document inspection information accurately on the Daily Inspection Report (DIR) and ensure all manufacturing specifications are correct and complete. Your role will involve inspecting work areas, monitoring in-process finished products, collecting data and samples, and determining final product disposition. Responsibilities • Perform daily inspections of production lines to ensure GMP compliance., • Document all inspection details including lot numbers, fill weights, and defects., • Ensure manufacturing specifications for components, labeling, and products are correct., • Inspect work areas for removal of previous products and verify readiness., • Monitor, sample, and inspect finished products for quality through appropriate tests., • Collect data and samples to support product disposition decisions., • Determine and verify final product disposition and apply disposition labels., • Identify and report discrepancies to Production and Quality teams., • Perform AQL inspections and execute Rework protocols as needed., • Initiate and log LIMS and Retain Samples, and print specifications from ERP systems., • Collect and ship samples as required by customers or Manufacturing Instructions., • Collect stability samples and execute Trials and Validations., • Review documentation for accuracy prior to submission to QA Release team., • Act as Lead QA Inspector in absence, ensuring proper production floor coverage., • Identify continuous improvement opportunities and promote a culture of quality., • 3+ years of quality experience in a regulated environment., • Strong understanding of GMPs, quality systems, and regulated manufacturing environments., • Working knowledge of AQL inspection standards and in-process quality control methods., • Familiarity with batch documentation and manufacturing specifications., • Proficiency in Microsoft Office Suite and ability to learn quality-related systems., • Experience with in-process quality inspections, line clearances, and documentation review., • Experience supporting trials, validations, rework activities, and sample collection., • Ability to interpret and follow SOPs, Work Instructions, and product specifications., • Excellent documentation accuracy and attention to detail., • Associate’s Degree in a scientific, technical, or related field, or equivalent experience., • Experience in a regulated industry (e.g., FDA, EPA), preferably in manufacturing or QA roles., • Prior exposure to continuous improvement and deviation identification., • Solid organizational, multitasking, and time-management skills. Medical Dental Vision Accidental/Life 401k + match Holidays, Vacation & Sick Time Workplace Type This is a fully onsite position in Orangeburg,NY. Application Deadline This position is anticipated to close on Mar 31, 2026. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I is embedded into our culture through: • Hiring diverse talent, • Maintaining an inclusive environment through persistent self-reflection, • Building a culture of care, engagement, and recognition with clear outcomes Our Bangalore, Hyderabad, Pune, and Chennai delivery centers are hubs of engineering expertise, with core capabilities in mechanical and electrical engineering, systems and software, and manufacturing engineering. Our teams deliver work across multiple industries including transportation, consumer and industrial products, and life sciences. We serve more than 4,500 clients, including many Fortune 500 brands. Learn more about how we can work together at actalentservices.com.