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.
$16.00 - $17.00 per Hour This is a hands-on, detail-critical QC position responsible for ensuring the quality, accuracy, and integrity of all incoming product before it enters our distribution channels. Key Responsibilities Advanced Product Inspection & Verification Conduct in-depth quality inspections of incoming product samples from each shipment using structured DG QC procedures. Verify accuracy in DGMS (Designer Greetings Management System), including: Correct imagery Accurate UPC codes Proper item numbers Packaging integrity Attribute alignment Review POs and manifests to validate accuracy of production and receipts. Interpret process sheets and compare production specs against delivered product. Issue Identification, Investigation & Escalation Independently identify printing errors, specification mismatches, color inconsistencies, material defects, and supplier-quality deviations.
Determine whether issues stem from:
Art-file discrepancies Manufacturing defects Packaging failures Perform extended QC reviews by pulling cases from inventory when patterns emerge. Escalate issues with documented evidence to QC leadership and provide professional recommendations. Cross-Department Collaboration Partner with Art, Warehouse, Operations, and QC leadership to resolve product discrepancies quickly and accurately.
Provide clear communication regarding:
Hold decisions Rework requirements Pull-backs Disposal/compactor actions Replacements needed for sample rooms Documentation & Quality Reporting Enter detailed QC notes into DGMS, including: PO numbers Manifest IDs Description of defects Corrective actions taken Additional recommendations Maintain high-quality records to support traceability, audits, and continuous improvement. Advanced Product Testing Conduct structured testing (30-day tests where applicable) to evaluate: Hang-tab strength (gift bags, roll wrap) Polybag durability and seal integrity Envelope warping, bending, and insert fit Signage resilience, color fidelity, and curling Provide written reports and findings to QC leadership. Final QC Disposition & Stock Movement Approve or reject product based on DG standards. Label, palletize, and prepare product for return to stock. Complete Back-to-Stock transfers accurately and notify Warehouse leadership. Required Skills & Experience 3+ years hands-on Quality Control experience in manufacturing, print production, consumer goods, or packaging. Strong understanding of QC principles, visual inspection standards, and defect classification. Ability to work with multiple departments and communicate QC findings clearly. Strong computer skills; able to learn DGMS and follow digital workflows. Ability to make informed recommendations based on inspection results. Exceptional attention to detail — must consistently notice small defects or irregularities. Physical Requirements Ability to lift heavy boxes and move product during inspections. Must be able to stand, walk, bend, and maneuver within a warehouse for extended periods. Comfortable working in a fast-paced, high-volume operations environment. Work Environment On-site, warehouse-based QC role in Edison, NJ. Daily collaboration with Warehouse, Art, QC Leadership, and Operations. Hands-on, interactive, and quality-driven work environment. × Apply Now
