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.
$20.00 per hour Join Our Growing Quality Team! Responsibilities Collect representative samples of raw materials, packaging components, bulk products, work-in-process materials, finished goods, and environmental monitoring samples. Perform sampling according to approved SOPs and sampling plans. Verify material identity, lot numbers, quantities, and labeling. Inspect incoming materials for damage, contamination, and labeling accuracy. Label, document, package, and submit samples to the Quality Control Laboratory. Maintain accurate sampling records, chain of custody documentation, and laboratory submission logs. Follow Good Documentation Practices (GDP), ALCOA+ principles, and cGMP requirements. Maintain sampling equipment, tools, and designated work areas. Collaborate with Warehouse, Production, Quality Assurance, Quality Control, Regulatory Affairs, and Supply Chain teams. Support audits, investigations, continuous improvement initiatives, and regulatory compliance. Required High School Diploma or GED Strong attention to detail and organizational skills Ability to follow SOPs and written procedures Basic computer and data entry skills Ability to lift up to 50 lbs. and work in a manufacturing environment Associate degree in Chemistry, Biology, Cosmetic Science, Quality Assurance, or a related scientific field 1-3 years of experience in Quality Assurance, Quality Control, laboratory, manufacturing, or sampling Experience in cosmetic, pharmaceutical, OTC, food, chemical, or CPG manufacturing Experience working in FDA-regulated and cGMP environments Preferred Knowledge Current Good Manufacturing Practices (cGMP) Good Documentation Practices (GDP)
ISO 22716
Cosmetic
GMP 21 CFR
Parts 210 & 211 Certificates of Analysis (COAs) Quality Management Systems (QMS) ERP systems Laboratory sample handling and chain of custody procedures Physical Requirements Stand and walk for extended periods Lift and move materials up to 50 pounds Bend, reach, and perform repetitive motions Work around manufacturing equipment, raw materials, fragrances, and chemicals Wear required PPE Apply today and become part of a team committed to quality, compliance, and operational excellence! 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
