Job Description Job Description Immediate Opening! Quality Control Inspector We are seeking a highly detail-oriented Quality Control Inspector to test and inspect materials, parts, and products at various stages of production. This role is ideal for a dedicated quality professional with a strong background in pharmaceutical or medical device regulations, meticulous documentation habits, and a collaborative approach to continuous improvement. Key Responsibilities Perform incoming, first article, in-process, and final inspections to ensure full compliance with company and regulatory standards Initiate nonconformance reports (NCR) for any non-conforming materials identified during operations Review, complete, and release manufacturing job order documents using Good Documentation Practices (GDP) Approve or reject raw materials based on established quality standards and communicate findings to all required parties Support cross-functional investigations into non-conformance findings and provide recommendations for process improvements Perform critical pre- and post-inspection steps for products undergoing the gamma irradiation process Compile quality metrics data and regularly submit structured reports to the QC Supervisor or Lead Maintain a safe, orderly workspace and wear full personal protective equipment (PPE) including scrubs, coveralls, masks, and eyewear in an ISO cleanroom environment Qualifications High School Diploma or equivalent required Minimum 3 years of experience in manufacturing quality control inspections At least 1 year of experience handling technical documentation and corrective actions in a pharmaceutical or medical device setting Working knowledge of global regulations, including

ISO 9001, ISO

13485, and 21 CFR Parts 210, 211, or 820 Proven ability to execute strict GMP operations by following detailed Standard Operating Procedures (SOPs) Hands-on experience using precision measuring devices such as calipers, rulers, tape measures, and pin gauges Solid basic mathematics, computer proficiency, and preferred working knowledge of ERP systems (such as SyteLine) Strong interpersonal and communication skills to effectively collaborate across internal departments and external vendors Why Join Us? Critical quality ownership role within a highly regulated, precision-driven manufacturing facility Opportunity to participate directly in continuous improvement initiatives and cross-functional team investigations Structured and safe work environment with an uncompromising commitment to compliance and product integrity Stable position offering professional growth in advanced pharmaceutical and medical device quality standards