A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
1st Shift (7:00 AM to 3:00 PM): $21.00/hour 2nd Shift (3:00 PM to 11:00 PM): $23.00/hour 3rd Shift (11:00 PM to 7:00 AM): $23.00/hour Position Summary ZING is seeking a detail-oriented Quality Control Line Inspector to perform in-process inspections on manufacturing and packaging lines to ensure cosmetic and OTC drug products are produced in compliance with current Good Manufacturing Practices (cGMP), internal quality standards, and applicable regulatory requirements. Responsibilities Perform routine in-process inspections on filling, labeling, and packaging lines. Verify line clearance prior to production start-up. Inspect fill levels, container integrity, labeling accuracy, and product coding. Identify and report defects such as leaks, mislabels, contamination, or damaged packaging. Ensure compliance with cGMP requirements, standard operating procedures (SOPs), and quality standards. Complete inspection logs, batch records, and deviation documentation accurately. Escalate quality concerns and support investigations of non-conforming products. Conduct line clearance activities during product changeovers. Verify the correct labels, cartons, containers, and packaging components are being used. Confirm proper material reconciliation. Collect in-process samples according to established sampling plans. Perform visual inspections and basic quality checks. Submit samples to the Quality Control laboratory as required. Review batch documentation to ensure compliance with Good Documentation Practices (GDP/ALCOA+). Collaborate with Production, Quality Assurance, and Warehouse teams. Support internal, customer, and regulatory audits. Requirements High school diploma or GED required. Associate degree preferred. 1+ year of experience in cosmetic, pharmaceutical, OTC, or other regulated manufacturing quality inspection. Experience working in an FDA-regulated manufacturing environment preferred. Working knowledge of current Good Manufacturing Practices (cGMP). Familiarity with FDA regulations, including 21 CFR Parts 210 and 211, is preferred. Strong attention to detail and documentation accuracy. Effective communication and problem escalation skills. Basic math and inspection skills. Ability to work in a fast-paced manufacturing environment. Ability to stand for extended periods. Ability to perform visual inspections throughout the shift. Ability to lift up to 50 pounds. Willingness to work overtime, weekends, or alternate shifts as needed. Work Environment Manufacturing environment requiring appropriate PPE. Standing for extended periods throughout the shift. Shift work, overtime, and weekend work may be required. ZING Recruiting is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, sexual orientation, and gender identity), national origin, age, disability, genetic information, or any other protected status under federal, state, or local law. We are committed to fostering a diverse and inclusive workplace. #ZINGZIP #ZINGNJ
